Variant report

Variant	nsv1041078
Chromosome Location	chr14:97001679-97279220
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3064)
CpG islands
(count:3790)
Chromatin interactive
region (count:235)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:3064 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:97113854-97114026	K562	blood:	n/a	n/a
2	ARID3A	chr14:97263366-97263797	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:97050635-97050712	K562	blood:	n/a	n/a
4	ARID3A	chr14:97275339-97275687	K562	blood:	n/a	n/a
5	ARID3A	chr14:97223125-97223507	K562	blood:	n/a	n/a
6	ARID3A	chr14:97126507-97126797	K562	blood:	n/a	n/a
7	ARID3A	chr14:97268957-97269728	K562	blood:	n/a	n/a
8	ARID3A	chr14:97030779-97030978	HepG2	liver:	n/a	n/a
9	ATF1	chr14:97148684-97148746	K562	blood:	n/a	n/a
10	ATF1	chr14:97171802-97172071	K562	blood:	n/a	n/a
11	ATF1	chr14:97263386-97263812	K562	blood:	n/a	n/a
12	ATF1	chr14:97126481-97126798	K562	blood:	n/a	n/a
13	ATF1	chr14:97026028-97026228	K562	blood:	n/a	n/a
14	ATF1	chr14:97273223-97273549	K562	blood:	n/a	n/a
15	ATF1	chr14:97047250-97047711	K562	blood:	n/a	n/a
16	ATF1	chr14:97275339-97275756	K562	blood:	n/a	n/a
17	ATF1	chr14:97102247-97102558	K562	blood:	n/a	n/a
18	ATF1	chr14:97151485-97151654	K562	blood:	n/a	n/a
19	ATF1	chr14:97268987-97269670	K562	blood:	n/a	n/a
20	ATF1	chr14:97270459-97270522	K562	blood:	n/a	n/a
21	ATF1	chr14:97223118-97224298	K562	blood:	n/a	n/a
22	ATF1	chr14:97241267-97241530	K562	blood:	n/a	n/a
23	ATF1	chr14:97228972-97229408	K562	blood:	n/a	n/a
24	ATF2	chr14:97165421-97165724	GM12878	blood:	n/a	n/a
25	ATF2	chr14:97165535-97165843	GM12878	blood:	n/a	n/a
26	ATF2	chr14:97263404-97263855	GM12878	blood:	n/a	n/a
27	ATF3	chr14:97273176-97273463	K562	blood:	n/a	n/a
28	ATF3	chr14:97228952-97229465	GM12878	blood:	n/a	n/a
29	ATF3	chr14:97154975-97155235	K562	blood:	n/a	n/a
30	ATF3	chr14:97229125-97229330	K562	blood:	n/a	n/a
31	ATF3	chr14:97129932-97130110	K562	blood:	n/a	n/a
32	ATF3	chr14:97229084-97229355	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr14:97229096-97229321	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF3	chr14:97269265-97269726	K562	blood:	n/a	n/a
35	ATF3	chr14:97263414-97263815	K562	blood:	n/a	n/a
36	ATF3	chr14:97229129-97229291	HepG2	liver:	n/a	n/a
37	ATF3	chr14:97263389-97263682	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr14:97196988-97197131	K562	blood:	n/a	n/a
39	BACH1	chr14:97263683-97264115	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr14:97027940-97027967	K562	blood:	n/a	n/a
41	BACH1	chr14:97224051-97224182	K562	blood:	n/a	n/a
42	BACH1	chr14:97266062-97266100	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr14:97207734-97208439	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr14:97223078-97223079	K562	blood:	n/a	n/a
45	BACH1	chr14:97093553-97093561	K562	blood:	n/a	n/a
46	BCL3	chr14:97263288-97263788	A549	lung:	n/a	chr14:97263703-97263716 chr14:97263610-97263619 chr14:97263569-97263577
47	BCLAF1	chr14:97269163-97269669	K562	blood:	n/a	n/a
48	BCLAF1	chr14:97263285-97263986	GM12878	blood:	n/a	chr14:97263703-97263716 chr14:97263932-97263945 chr14:97263610-97263619 chr14:97263569-97263577 chr14:97263946-97263955
49	BHLHE40	chr14:97263450-97263858	HepG2	liver:	n/a	chr14:97263701-97263717
50	BHLHE40	chr14:97129978-97130201	K562	blood:	n/a	n/a

(count:3790 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97205952-97206002	HL-60	blood:	n/a
2	chr14:97206170-97206220	MCF10A-Er-Src	breast:	n/a
3	chr14:97059243-97059293	ovcar-3	ovarian:	n/a
4	chr14:97205952-97206002	NHDF-neo	bronchial:	n/a
5	chr14:97031960-97032010	ProgFib	skin:	n/a
6	chr14:97206170-97206220	NHBE	bronchial:	n/a
7	chr14:97092150-97092200	HCPEpiC	choroid plexus:	n/a
8	chr14:97091520-97091570	Hela-S3	cervix:	n/a
9	chr14:97205952-97206002	HL-60	blood:	n/a
10	chr14:97206170-97206220	MCF10A-Er-Src	breast:	n/a
11	chr14:97059243-97059293	ovcar-3	ovarian:	n/a
12	chr14:97205952-97206002	NHDF-neo	bronchial:	n/a
13	chr14:97031960-97032010	ProgFib	skin:	n/a
14	chr14:97206170-97206220	NHBE	bronchial:	n/a
15	chr14:97092150-97092200	HCPEpiC	choroid plexus:	n/a
16	chr14:97091520-97091570	Hela-S3	cervix:	n/a
17	chr14:97055808-97055858	HRCEpiC	kidney:	n/a
18	chr14:97205952-97206002	PrEC	prostate:	n/a
19	chr14:97262871-97262921	LNCaP	prostate:	n/a
20	chr14:97059192-97059242	HRPEpiC	eye:	n/a
21	chr14:97263710-97263760	HIPEpiC	eye:	n/a
22	chr14:97058777-97058827	AG10803	skin:	n/a
23	chr14:97264013-97264063	HRCEpiC	kidney:	n/a
24	chr14:97263524-97263574	NHBE	bronchial:	n/a
25	chr14:97031960-97032010	K562	blood:	n/a
26	chr14:97267126-97267176	BE2_C	brain:	n/a
27	chr14:97165297-97165347	MCF10A-Er-Src	breast:	n/a
28	chr14:97129577-97129627	AG04450	lung:	fetal
29	chr14:97061349-97061399	CMK	blood:	n/a
30	chr14:97208170-97208220	AG09319	gingival:	n/a
31	chr14:97081558-97081608	HEEpiC	esophagus:	n/a
32	chr14:97135129-97135179	PFSK-1	brain:	n/a
33	chr14:97129577-97129627	PFSK-1	brain:	n/a
34	chr14:97208170-97208220	H1-hESC	embryonic stem cell:	embryo
35	chr14:97059467-97059517	K562	blood:	n/a
36	chr14:97267126-97267176	GM12891	blood:	n/a
37	chr14:97207786-97207836	NHDF-neo	bronchial:	n/a
38	chr14:97092205-97092255	NH-A	brain:	n/a
39	chr14:97059349-97059399	Caco-2	colon:	n/a
40	chr14:97262732-97262782	AG10803	skin:	n/a
41	chr14:97263458-97263508	HRCEpiC	kidney:	n/a
42	chr14:97055808-97055858	SK-N-SH_RA	brain:	n/a
43	chr14:97059243-97059293	Caco-2	colon:	n/a
44	chr14:97211894-97211944	BJ	skin:	n/a
45	chr14:97208114-97208164	A549	lung:	n/a
46	chr14:97208245-97208295	IMR90	lung:	fetal
47	chr14:97059349-97059399	AG10803	skin:	n/a
48	chr14:97208170-97208220	PrEC	prostate:	n/a
49	chr14:97092150-97092200	AG10803	skin:	n/a
50	chr14:97263643-97263693	HCF	heart:	n/a

(count:235 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr14:97265880..97270207-chr14:97278911..97281407,6	K562	blood:
2	chr14:97039485..97041409-chr14:97041476..97043217,2	K562	blood:
3	chr14:97244728..97247243-chr14:97260484..97262767,2	K562	blood:
4	chr14:97262824..97265554-chr14:97270271..97273136,2	MCF-7	breast:
5	chr14:96967004..96969133-chr14:97009562..97011863,2	MCF-7	breast:
6	chr14:97270252..97272755-chr14:97275339..97277575,4	K562	blood:
7	chr14:97221085..97223610-chr14:97225132..97227654,2	MCF-7	breast:
8	chr14:97043094..97045370-chr14:97047033..97048626,2	K562	blood:
9	chr14:97130230..97132435-chr14:97152874..97154643,2	MCF-7	breast:
10	chr14:97121918..97124905-chr14:97127753..97129733,2	K562	blood:
11	chr14:97100866..97101454-chr14:97138053..97138598,2	MCF-7	breast:
12	chr14:97263731..97266819-chr14:97323461..97326778,3	K562	blood:
13	chr14:97270310..97272481-chr14:97294425..97296809,2	K562	blood:
14	chr14:97125727..97128111-chr14:97129743..97131813,3	K562	blood:
15	chr14:97265808..97269390-chr14:97269409..97272897,4	MCF-7	breast:
16	chr14:96967059..96970873-chr14:97003621..97006595,4	K562	blood:
17	chr14:97253752..97255337-chr14:97258116..97260062,2	K562	blood:
18	chr14:97251859..97256627-chr14:97261114..97265301,5	K562	blood:
19	chr14:97265808..97269390-chr14:97269409..97272897,4	MCF-7	breast:
20	chr14:97050265..97051308-chr14:97136874..97138151,3	MCF-7	breast:
21	chr14:96998656..97003736-chr14:97006318..97010679,5	MCF-7	breast:
22	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
23	chr14:97199537..97202098-chr14:97275666..97277302,2	K562	blood:
24	chr14:95522595..95523324-chr14:97032688..97033240,2	MCF-7	breast:
25	chr14:97266936..97268792-chr14:97269139..97271889,2	MCF-7	breast:
26	chr14:97127931..97131812-chr14:97133536..97135209,3	K562	blood:
27	chr14:97041013..97042090-chr14:97100546..97101489,8	MCF-7	breast:
28	chr14:97125727..97128111-chr14:97129743..97131813,3	K562	blood:
29	chr14:97100866..97101454-chr14:97138053..97138598,2	MCF-7	breast:
30	chr14:97050324..97051208-chr14:97145144..97146022,4	MCF-7	breast:
31	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
32	chr14:97050494..97051205-chr14:97646447..97647466,5	MCF-7	breast:
33	chr14:97075091..97077466-chr14:97079393..97081183,2	MCF-7	breast:
34	chr14:97040936..97041835-chr14:97100556..97101428,4	MCF-7	breast:
35	chr14:97050283..97051241-chr14:99732793..99733539,2	K562	blood:
36	chr14:97040936..97041835-chr14:97100556..97101428,4	MCF-7	breast:
37	chr14:97061336..97063111-chr14:97065431..97067528,2	K562	blood:
38	chr14:97050319..97051064-chr14:97320992..97321806,2	MCF-7	breast:
39	chr14:97272734..97276764-chr14:97276840..97280627,4	K562	blood:
40	chr14:97133535..97135440-chr14:97140308..97142145,2	MCF-7	breast:
41	chr14:97047308..97047841-chr14:97100928..97101485,2	MCF-7	breast:
42	chr14:97079988..97082344-chr14:97083126..97085624,2	MCF-7	breast:
43	chr14:97049647..97051758-chr14:97207410..97208429,16	MCF-7	breast:
44	chr14:97053592..97055539-chr14:97067888..97070552,2	MCF-7	breast:
45	chr14:97263932..97266038-chr14:97266708..97268317,2	MCF-7	breast:
46	chr14:97096962..97100936-chr14:97101885..97104048,3	K562	blood:
47	chr14:97263560..97266144-chr14:97273752..97276345,2	MCF-7	breast:
48	chr14:97191718..97193333-chr14:97193874..97196333,2	MCF-7	breast:
49	chr14:97252075..97254821-chr14:97254880..97257598,2	K562	blood:
50	chr14:97050566..97051176-chr14:97145157..97145895,3	MCF-7	breast:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG2B-9	chr14:97209419-97209532	ucscGeneNc_uc001yfv_1
2	lnc-PAPOLA-1	chr14:97059827-97060036	XLOC_010920
3	lnc-PAPOLA-1	chr14:97061001-97061097	ENSG00000258702.1
4	lnc-PAPOLA-1	chr14:97059458-97059586	XLOC_010920
5	lnc-VRK1-2	chr14:97207528-97207548	ENSG00000258979
6	lnc-VRK1-2	chr14:97256709-97257011	XLOC_010921
7	lnc-PAPOLA-1	chr14:97059827-97062437	XLOC_010920
8	lnc-PAPOLA-1	chr14:97061001-97062356	XLOC_010920
9	lnc-AK7-5	chr14:97028795-97029230	NONHSAT039542
10	lnc-PAPOLA-1	chr14:97059070-97062099	ENSG00000258702.1
11	lnc-PAPOLA-1	chr14:97059827-97059916	NONHSAT039548
12	lnc-VRK1-2	chr14:97256709-97256950	ENSG00000258979
13	lnc-VRK1-2	chr14:97229347-97229452	XLOC_010921
14	lnc-ATG2B-9	chr14:97182252-97182462	ucscGeneNc_uc001yfv_1
15	lnc-PAPOLA-1	chr14:97059105-97059586	ENSG00000258702.1
16	lnc-PAPOLA-1	chr14:97059444-97059586	NONHSAT039548
17	lnc-PAPOLA-1	chr14:97059458-97059586	XLOC_010920
18	lnc-ATG2B-9	chr14:97168771-97169781	ucscGeneNc_uc001yfv_1
19	lnc-PAPOLA-1	chr14:97059347-97059586	XLOC_010920
20	lnc-PAPOLA-1	chr14:97059827-97060036	ENSG00000258702.1
21	lnc-PAPOLA-1	chr14:97061001-97061619	NONHSAT039548
22	lnc-VRK1-2	chr14:97210498-97210606	ENSG00000258979
23	lnc-PAPOLA-1	chr14:97059070-97061767	NONHSAT039545
24	lnc-PAPOLA-1	chr14:97059040-97059152	XLOC_010920
25	lnc-ATG2B-8	chr14:97104524-97104851	NONHSAT039549
26	lnc-VRK1-2	chr14:97219606-97219663	ENSG00000258979
27	lnc-AK7-5	chr14:97031292-97031443	NONHSAT039542
28	lnc-ATG2B-9	chr14:97222449-97222748	ucscGeneNc_uc001yfv_1
29	lnc-PAPOLA-1	chr14:97059124-97059152	XLOC_010920
30	lnc-PAPOLA-1	chr14:97062078-97062088	NONHSAT039545
31	lnc-PAPOLA-1	chr14:97061001-97062093	XLOC_010920
32	lnc-PAPOLA-1	chr14:97059827-97060036	XLOC_010920

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PAPOLA	hsa-miR-320a	chr14:97031785-97031808
2	PAPOLA	hsa-miR-93-5p	chr14:97031736-97031760
3	PAPOLA	hsa-miR-155-5p	chr14:97031585-97031607
4	PAPOLA	hsa-miR-93-5p	chr14:97031753-97031759

Variant related genes	Relation type
ENSG00000258702	TF binding region
ENSG00000258979	TF binding region
PAPOLA	TF binding region
VRK1	TF binding region
RN7SKP108	TF binding region
ENSG00000258702	CpG island
ENSG00000258979	CpG island
PAPOLA	CpG island
VRK1	CpG island
RN7SKP108	CpG island
ENSG00000144366	chromatin interactions
ENSG00000270141	chromatin interactions
ENSG00000260806	chromatin interactions
ENSG00000196405	chromatin interactions
ENSG00000077152	chromatin interactions
ENSG00000100749	chromatin interactions
ENSG00000072736	chromatin interactions
ENSG00000258979	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000258702	chromatin interactions

Extended variants
information (count: 10533 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:10533 , 50 per page) page: 1 2 3 4 5 6 7 ... 211

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577826546	chr14:97001695-97001696	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs545361997	chr14:97001742-97001743	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376623800	chr14:97001766-97001767	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs564469037	chr14:97001796-97001797	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs529076607	chr14:97001929-97001930	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531767804	chr14:97001930-97001931	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs34390783	chr14:97001937-97001938	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs543853265	chr14:97001978-97001979	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs562136382	chr14:97002017-97002018	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs529373405	chr14:97002046-97002047	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374523706	chr14:97002059-97002060	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs144765554	chr14:97002068-97002069	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566184488	chr14:97002119-97002120	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs559642134	chr14:97002144-97002145	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs374018438	chr14:97002168-97002169	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs151075600	chr14:97002175-97002176	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs371361604	chr14:97002201-97002202	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs373329661	chr14:97002211-97002212	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs144379355	chr14:97002284-97002285	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs200442417	chr14:97002297-97002298	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs140991527	chr14:97002317-97002318	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs376875671	chr14:97002343-97002344	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs150210401	chr14:97002345-97002346	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183696650	chr14:97002354-97002355	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373009601	chr14:97002355-97002356	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs373110862	chr14:97002359-97002360	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs377329684	chr14:97002369-97002370	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs187787582	chr14:97002433-97002434	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs190312449	chr14:97002464-97002465	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs113891738	chr14:97002513-97002514	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs528420080	chr14:97002517-97002518	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs377387329	chr14:97002530-97002531	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs557259101	chr14:97002587-97002588	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs183048499	chr14:97002656-97002657	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs186973042	chr14:97002677-97002678	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561948767	chr14:97002694-97002695	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs191828389	chr14:97002695-97002696	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs530468902	chr14:97002706-97002707	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs200071545	chr14:97002712-97002713	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs541215740	chr14:97002781-97002782	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs184376835	chr14:97002833-97002834	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs533385824	chr14:97002835-97002836	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs551571818	chr14:97002857-97002858	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs567256447	chr14:97002861-97002862	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187512644	chr14:97002908-97002909	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs78417558	chr14:97002938-97002939	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs548531752	chr14:97002974-97002975	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs369319705	chr14:97002979-97002980	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs567192892	chr14:97002991-97002992	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs192749774	chr14:97002994-97002995	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
Cancer	20164920	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Breast cancer	21509527	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	17426248	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:3140 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:96978000-97019400	Weak transcription	Aorta	Aorta
2	chr14:96979600-97022400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:96979800-97019200	Weak transcription	Small Intestine	intestine
4	chr14:96980800-97020600	Weak transcription	Stomach Mucosa	stomach
5	chr14:96982000-97031400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr14:96984800-97020800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:96984800-97039400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr14:96985800-97004800	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr14:96985800-97005200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:96986000-97003800	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr14:96986000-97004800	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr14:96986200-97004400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr14:96986200-97005600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr14:96986400-97002800	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr14:96986400-97002800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr14:96986400-97002800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr14:96986400-97003000	Strong transcription	Duodenum Mucosa	Duodenum
18	chr14:96986400-97005400	Strong transcription	Placenta	Placenta
19	chr14:96986400-97007200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr14:96986600-97003800	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr14:96986600-97005200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:96986600-97006200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:96986800-97003800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:96986800-97006800	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr14:96987000-97002400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr14:96987000-97002600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
27	chr14:96987000-97003000	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr14:96987200-97002800	Strong transcription	Primary B cells from cord blood	blood
29	chr14:96987200-97003800	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr14:96987200-97004000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr14:96987200-97004400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr14:96987200-97004400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr14:96987200-97010200	Weak transcription	HSMMtube	muscle
34	chr14:96987400-97003000	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr14:96987400-97003800	Strong transcription	Primary B cells from peripheral blood	blood
36	chr14:96987800-97003800	Strong transcription	Dnd41	blood
37	chr14:96988200-97012600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:96989000-97018800	Weak transcription	Lung	lung
39	chr14:96989200-97018600	Weak transcription	Brain Substantia Nigra	brain
40	chr14:96991000-97004000	Strong transcription	Fetal Intestine Large	intestine
41	chr14:96991400-97022400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr14:96992200-97011600	Weak transcription	NHLF	lung
43	chr14:96993000-97018800	Weak transcription	Gastric	stomach
44	chr14:96993000-97018800	Weak transcription	Pancreas	Pancrea
45	chr14:96993000-97018800	Weak transcription	Spleen	Spleen
46	chr14:96993200-97012400	Weak transcription	Right Ventricle	heart
47	chr14:96993200-97018800	Weak transcription	Esophagus	oesophagus
48	chr14:96993600-97002200	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr14:96993600-97017400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr14:96993600-97018800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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