Variant report

Variant	nsv830455
Chromosome Location	chr5:114761542-114938284
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3250)
CpG islands
(count:2627)
Chromatin interactive
region (count:119)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3250 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:114799770-114800052	K562	blood:	n/a	n/a
2	ARID3A	chr5:114880322-114880976	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:114880325-114880472	K562	blood:	n/a	n/a
4	ARID3A	chr5:114887023-114887344	K562	blood:	n/a	n/a
5	ARID3A	chr5:114922230-114922547	K562	blood:	n/a	n/a
6	ARID3A	chr5:114890940-114891103	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:114922287-114922759	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:114875815-114876014	K562	blood:	n/a	n/a
9	ATF1	chr5:114799811-114799998	K562	blood:	n/a	n/a
10	ATF1	chr5:114790917-114791113	K562	blood:	n/a	n/a
11	ATF1	chr5:114880294-114880673	K562	blood:	n/a	n/a
12	ATF2	chr5:114795970-114796493	GM12878	blood:	n/a	n/a
13	ATF2	chr5:114937281-114937791	GM12878	blood:	n/a	n/a
14	ATF2	chr5:114880186-114880585	GM12878	blood:	n/a	n/a
15	ATF2	chr5:114880030-114880572	GM12878	blood:	n/a	n/a
16	ATF2	chr5:114830009-114830685	GM12878	blood:	n/a	n/a
17	ATF2	chr5:114796051-114796480	GM12878	blood:	n/a	n/a
18	ATF2	chr5:114937958-114938507	GM12878	blood:	n/a	n/a
19	ATF2	chr5:114880183-114880603	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:114914152-114914766	GM12878	blood:	n/a	n/a
21	ATF2	chr5:114913231-114913974	GM12878	blood:	n/a	n/a
22	ATF2	chr5:114830093-114830646	GM12878	blood:	n/a	n/a
23	ATF2	chr5:114937257-114937744	GM12878	blood:	n/a	n/a
24	ATF2	chr5:114915115-114916084	GM12878	blood:	n/a	n/a
25	ATF2	chr5:114914848-114916000	GM12878	blood:	n/a	n/a
26	ATF2	chr5:114823254-114823947	GM12878	blood:	n/a	n/a
27	ATF2	chr5:114823298-114823787	GM12878	blood:	n/a	n/a
28	ATF2	chr5:114880599-114881056	GM12878	blood:	n/a	n/a
29	ATF2	chr5:114913373-114913930	GM12878	blood:	n/a	n/a
30	ATF2	chr5:114914216-114914802	GM12878	blood:	n/a	n/a
31	ATF3	chr5:114938066-114938296	K562	blood:	n/a	n/a
32	BACH1	chr5:114938065-114938286	K562	blood:	n/a	n/a
33	BACH1	chr5:114805491-114805506	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr5:114937814-114938326	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr5:114924913-114924931	K562	blood:	n/a	n/a
36	BACH1	chr5:114895452-114895462	K562	blood:	n/a	n/a
37	BATF	chr5:114823362-114823699	GM12878	blood:	n/a	n/a
38	BATF	chr5:114913443-114913938	GM12878	blood:	n/a	n/a
39	BATF	chr5:114938019-114938314	GM12878	blood:	n/a	n/a
40	BATF	chr5:114797164-114797567	GM12878	blood:	n/a	chr5:114797403-114797412
41	BATF	chr5:114796027-114796555	GM12878	blood:	n/a	chr5:114796271-114796282 chr5:114796272-114796282
42	BATF	chr5:114913443-114913854	GM12878	blood:	n/a	n/a
43	BATF	chr5:114914378-114914734	GM12878	blood:	n/a	n/a
44	BATF	chr5:114937319-114937692	GM12878	blood:	n/a	n/a
45	BATF	chr5:114915352-114915680	GM12878	blood:	n/a	n/a
46	BATF	chr5:114797231-114797570	GM12878	blood:	n/a	chr5:114797403-114797412
47	BATF	chr5:114915322-114915800	GM12878	blood:	n/a	n/a
48	BATF	chr5:114808363-114808561	GM12878	blood:	n/a	chr5:114808465-114808474
49	BATF	chr5:114887194-114887495	GM12878	blood:	n/a	chr5:114887351-114887361 chr5:114887355-114887365 chr5:114887350-114887361
50	BATF	chr5:114937295-114937797	GM12878	blood:	n/a	n/a

(count:2627 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:114880771-114880821	RPTEC	kidney:	n/a
2	chr5:114880745-114880795	A549	lung:	n/a
3	chr5:114849119-114849169	SK-N-MC	brain:	n/a
4	chr5:114937614-114937664	GM06990	blood:	n/a
5	chr5:114880771-114880821	RPTEC	kidney:	n/a
6	chr5:114880745-114880795	A549	lung:	n/a
7	chr5:114849119-114849169	SK-N-MC	brain:	n/a
8	chr5:114937614-114937664	GM06990	blood:	n/a
9	chr5:114937919-114937969	SK-N-MC	brain:	n/a
10	chr5:114895062-114895112	PrEC	prostate:	n/a
11	chr5:114879806-114879856	HIPEpiC	eye:	n/a
12	chr5:114880508-114880558	HEEpiC	esophagus:	n/a
13	chr5:114791124-114791174	GM19239	blood:	n/a
14	chr5:114880796-114880846	GM12878	blood:	n/a
15	chr5:114880381-114880431	SAEC	small airway:	n/a
16	chr5:114880667-114880717	Jurkat	blood:	n/a
17	chr5:114762855-114762905	GM19239	blood:	n/a
18	chr5:114934133-114934183	K562	blood:	n/a
19	chr5:114937614-114937664	Jurkat	blood:	n/a
20	chr5:114880715-114880765	SK-N-SH	brain:	n/a
21	chr5:114935797-114935847	AG09309	skin:	n/a
22	chr5:114764748-114764798	GM12891	blood:	n/a
23	chr5:114895062-114895112	HPAEpiC	pulmonary alveolar:	n/a
24	chr5:114880330-114880380	NHDF-neo	bronchial:	n/a
25	chr5:114879806-114879856	Jurkat	blood:	n/a
26	chr5:114934133-114934183	LNCaP	prostate:	n/a
27	chr5:114849140-114849190	U87	brain:	n/a
28	chr5:114879806-114879856	NHBE	bronchial:	n/a
29	chr5:114916433-114916483	GM12891	blood:	n/a
30	chr5:114937784-114937834	ProgFib	skin:	n/a
31	chr5:114937784-114937834	HRE	kidney:	n/a
32	chr5:114879581-114879631	AG04450	lung:	fetal
33	chr5:114849010-114849060	NB4	blood:	n/a
34	chr5:114887230-114887280	MCF10A-Er-Src	breast:	n/a
35	chr5:114880381-114880431	HAEpiC	amniotic membrane:	n/a
36	chr5:114849140-114849190	HIPEpiC	eye:	n/a
37	chr5:114937614-114937664	MCF10A-Er-Src	breast:	n/a
38	chr5:114884044-114884094	AG04450	lung:	fetal
39	chr5:114849010-114849060	U87	brain:	n/a
40	chr5:114807774-114807824	HCT-116	colon:	n/a
41	chr5:114916433-114916483	AG09319	gingival:	n/a
42	chr5:114879687-114879737	AG04450	lung:	fetal
43	chr5:114938148-114938198	HMEC	breast:	n/a
44	chr5:114849010-114849060	HUVEC	blood vessel:	n/a
45	chr5:114937919-114937969	IMR90	lung:	fetal
46	chr5:114934133-114934183	HEK293	kidney:	embryo
47	chr5:114791124-114791174	GM12878	blood:	n/a
48	chr5:114938236-114938286	GM12891	blood:	n/a
49	chr5:114937919-114937969	GM12878	blood:	n/a
50	chr5:114880796-114880846	K562	blood:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:114841716..114844376-chr5:114856234..114858022,2	MCF-7	breast:
2	chr5:114712822..114713353-chr5:114921928..114922705,2	MCF-7	breast:
3	chr5:114761971..114764716-chr5:114811734..114814412,2	MCF-7	breast:
4	chr5:114840582..114843514-chr5:114878687..114880300,2	K562	blood:
5	chr5:114930114..114932547-chr5:114952290..114954569,2	K562	blood:
6	chr5:114903873..114906375-chr5:114910655..114912171,2	MCF-7	breast:
7	chr5:114869947..114871868-chr5:114902039..114905014,2	K562	blood:
8	chr5:114934770..114936777-chr5:114950796..114953360,2	K562	blood:
9	chr5:114823853..114826321-chr5:114827357..114829571,2	K562	blood:
10	chr5:114877886..114879457-chr5:114935009..114937600,2	K562	blood:
11	chr5:114840340..114842115-chr5:114845150..114846853,2	K562	blood:
12	chr5:114934250..114936093-chr5:114941092..114942888,2	MCF-7	breast:
13	chr5:114880215..114881730-chr5:114959993..114961960,2	K562	blood:
14	chr5:114869947..114871868-chr5:114902039..114905014,2	K562	blood:
15	chr5:114893635..114896285-chr5:114902455..114905206,2	MCF-7	breast:
16	chr5:114825113..114827220-chr5:114830397..114832433,2	MCF-7	breast:
17	chr5:114856363..114859247-chr5:114859922..114862071,2	K562	blood:
18	chr5:114845762..114847363-chr5:114855311..114858213,2	K562	blood:
19	chr5:114934667..114936866-chr5:114947563..114949959,2	K562	blood:
20	chr5:114873536..114875419-chr5:114960010..114961720,2	K562	blood:
21	chr5:114891420..114893149-chr5:114895048..114897672,2	K562	blood:
22	chr5:114845762..114847363-chr5:114855311..114858213,2	K562	blood:
23	chr5:114903873..114906375-chr5:114910655..114912171,2	MCF-7	breast:
24	chr5:114860835..114862684-chr5:114863168..114864729,2	MCF-7	breast:
25	chr5:114857751..114862120-chr5:114862571..114865082,5	K562	blood:
26	chr5:114856543..114858049-chr5:115420611..115422224,2	MCF-7	breast:
27	chr5:114749201..114751602-chr5:114786972..114789566,2	K562	blood:
28	chr5:114857751..114862120-chr5:114862571..114865082,5	K562	blood:
29	chr5:114872131..114874195-chr5:114874384..114876871,2	MCF-7	breast:
30	chr5:114878325..114881784-chr5:114886706..114888930,3	MCF-7	breast:
31	chr17:46048149..46048819-chr5:114879946..114880664,2	NB4	blood:
32	chr5:114787173..114789116-chr5:114797971..114800586,2	MCF-7	breast:
33	chr5:114713336..114714974-chr5:114920219..114921988,2	MCF-7	breast:
34	chr5:114884990..114887012-chr5:114894509..114897041,2	K562	blood:
35	chr5:114870046..114871711-chr5:114873556..114876513,2	MCF-7	breast:
36	chr5:114828364..114830864-chr5:114831434..114833524,2	MCF-7	breast:
37	chr5:114891420..114893149-chr5:114895048..114897672,2	K562	blood:
38	chr5:114872131..114874195-chr5:114874384..114876871,2	MCF-7	breast:
39	chr5:114933628..114936434-chr5:114936724..114940118,4	MCF-7	breast:
40	chr5:114645138..114646056-chr5:114908059..114908645,2	MCF-7	breast:
41	chr5:114785383..114787402-chr5:114806966..114809373,2	MCF-7	breast:
42	chr5:114908239..114910015-chr5:114914437..114916676,2	MCF-7	breast:
43	chr5:114884946..114886999-chr5:114921116..114924631,3	K562	blood:
44	chr5:114823713..114825523-chr5:114959295..114961713,2	K562	blood:
45	chr5:114815800..114817948-chr5:114820554..114822975,2	MCF-7	breast:
46	chr5:114630084..114632961-chr5:114870291..114872236,2	K562	blood:
47	chr5:114893635..114896285-chr5:114902455..114905206,2	MCF-7	breast:
48	chr5:114851275..114854449-chr5:114878994..114881449,3	MCF-7	breast:
49	chr5:114708411..114710984-chr5:114878847..114880354,2	MCF-7	breast:
50	chr5:114884990..114887012-chr5:114894509..114897041,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMED7-3	chr5:114937794-114937886	NONHSAT103310
2	lnc-AP3S1-4	chr5:114937852-114938157	NR_109874
3	lnc-TMED7-3	chr5:114917427-114917621	NONHSAT103310
4	lnc-AP3S1-12	chr5:114829254-114829518	NONHSAT103305
5	lnc-AP3S1-9	chr5:114914612-114915030	NONHSAT103309
6	lnc-AP3S1-13	chr5:114825331-114825628	NONHSAT103304
7	lnc-AP3S1-4	chr5:114937852-114938157	NR_109875
8	lnc-AP3S1-11	chr5:114913244-114913454	NONHSAT103307
9	lnc-AP3S1-11	chr5:114910746-114913269	NONHSAT103306
10	lnc-AP3S1-4	chr5:114937844-114938157	NONHSAT103312
11	lnc-AP3S1-10	chr5:114914347-114914598	NONHSAT103308

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FEM1C	hsa-miR-103a-3p	chr5:114859110-114859133
2	FEM1C	hsa-miR-93-5p	chr5:114858541-114858534
3	FEM1C	hsa-miR-103a-3p	chr5:114859116-114859110
4	FEM1C	hsa-miR-93-5p	chr5:114858535-114858557
5	FEM1C	hsa-miR-16-5p	chr5:114859109-114859129

Variant related genes	Relation type
ENSG00000249944	TF binding region
ENSG00000249249	TF binding region
CCT5P1	TF binding region
TICAM2	TF binding region
ENSG00000249433	TF binding region
FEM1C	TF binding region
ENSG00000249944	CpG island
ENSG00000249249	CpG island
CCT5P1	CpG island
TICAM2	CpG island
ENSG00000249433	CpG island
FEM1C	CpG island
ENSG00000145781	chromatin interactions
ENSG00000243414	chromatin interactions
ENSG00000271918	chromatin interactions
ENSG00000164221	chromatin interactions
ENSG00000249249	chromatin interactions
ENSG00000251201	chromatin interactions
ENSG00000152503	chromatin interactions
ENSG00000108465	chromatin interactions
ENSG00000145780	chromatin interactions
ENSG00000134970	chromatin interactions
ENSG00000177879	chromatin interactions
ENSG00000145782	chromatin interactions
ENSG00000249433	chromatin interactions
ENSG00000250444	chromatin interactions
ENSG00000124523	chromatin interactions
ENSG00000249944	chromatin interactions
ENSG00000092203	chromatin interactions

Extended variants
information (count: 6724 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6724 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71579498	chr5:114761593-114761594	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192573767	chr5:114761596-114761597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71579499	chr5:114761601-114761602	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs544946530	chr5:114761632-114761633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566506373	chr5:114761649-114761650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548521034	chr5:114761703-114761704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535403003	chr5:114761720-114761721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141679564	chr5:114761733-114761734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540714635	chr5:114761737-114761738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568812403	chr5:114761831-114761832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538054677	chr5:114761873-114761874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557707010	chr5:114761903-114761904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150546159	chr5:114761917-114761918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577763792	chr5:114761939-114761940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565732197	chr5:114761965-114761966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533864958	chr5:114761985-114761986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79845585	chr5:114761987-114761988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111885960	chr5:114762016-114762017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200319351	chr5:114762021-114762022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201281693	chr5:114762038-114762039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183533892	chr5:114762039-114762040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs5010267	chr5:114762055-114762056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181241198	chr5:114762057-114762058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs3072102	chr5:114762058-114762059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs28435620	chr5:114762059-114762060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs5010268	chr5:114762071-114762072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs66513657	chr5:114762075-114762076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60603984	chr5:114762081-114762082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs60258042	chr5:114762085-114762086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145474642	chr5:114762099-114762100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369159216	chr5:114762126-114762127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573712651	chr5:114762140-114762141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116192230	chr5:114762175-114762176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559942058	chr5:114762179-114762180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186514114	chr5:114762216-114762217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576421353	chr5:114762235-114762236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545477459	chr5:114762257-114762258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190232764	chr5:114762294-114762295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139371668	chr5:114762317-114762318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs56130134	chr5:114762364-114762365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527869823	chr5:114762368-114762369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144153577	chr5:114762408-114762409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73783136	chr5:114762409-114762410	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs181496053	chr5:114762455-114762456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528898369	chr5:114762482-114762483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548660356	chr5:114762540-114762541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146485136	chr5:114762541-114762542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186151204	chr5:114762544-114762545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190917833	chr5:114762588-114762589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183502382	chr5:114762598-114762599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD
Renal cell carcinoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:4120 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114754000-114761600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:114754800-114766800	Weak transcription	Fetal Intestine Large	intestine
3	chr5:114755200-114762200	Weak transcription	Fetal Intestine Small	intestine
4	chr5:114756400-114761600	Weak transcription	NH-A	brain
5	chr5:114756400-114762200	Weak transcription	Small Intestine	intestine
6	chr5:114758000-114762400	Enhancers	Left Ventricle	heart
7	chr5:114758000-114762400	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr5:114758000-114762800	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr5:114758600-114765400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr5:114759400-114762200	Weak transcription	A549	lung
11	chr5:114759400-114766000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:114759600-114761600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:114759600-114761800	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr5:114759600-114762200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr5:114759600-114762200	Weak transcription	Osteobl	bone
16	chr5:114759600-114764400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr5:114759600-114764600	Weak transcription	Aorta	Aorta
18	chr5:114759600-114766000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:114759600-114766200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr5:114759800-114761600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr5:114759800-114762200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr5:114759800-114762200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr5:114759800-114764400	Weak transcription	Gastric	stomach
24	chr5:114759800-114767800	Weak transcription	Esophagus	oesophagus
25	chr5:114760000-114761600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr5:114760000-114761600	Weak transcription	NHDF-Ad	bronchial
27	chr5:114760000-114762200	Weak transcription	NHLF	lung
28	chr5:114760000-114763600	Weak transcription	Stomach Mucosa	stomach
29	chr5:114760000-114764400	Weak transcription	Psoas Muscle	Psoas
30	chr5:114760000-114765400	Weak transcription	Pancreas	Pancrea
31	chr5:114760200-114761600	Weak transcription	HSMM	muscle
32	chr5:114760200-114762200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr5:114760200-114763800	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr5:114760400-114761600	Weak transcription	Rectal Smooth Muscle	rectum
35	chr5:114760400-114762800	Enhancers	Stomach Smooth Muscle	stomach
36	chr5:114760400-114764200	Weak transcription	Fetal Muscle Leg	muscle
37	chr5:114760400-114766800	Weak transcription	Lung	lung
38	chr5:114760400-114767200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr5:114760600-114761600	Weak transcription	Colonic Mucosa	Colon
40	chr5:114760600-114761600	Weak transcription	Right Ventricle	heart
41	chr5:114760600-114762200	Weak transcription	HSMMtube	muscle
42	chr5:114761000-114762600	Enhancers	Colon Smooth Muscle	Colon
43	chr5:114761400-114761600	Enhancers	Fetal Heart	heart
44	chr5:114761400-114762000	Enhancers	Right Atrium	heart
45	chr5:114761400-114762800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:114761400-114763000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:114761600-114761800	Enhancers	Colonic Mucosa	Colon
48	chr5:114761600-114761800	Enhancers	Right Ventricle	heart
49	chr5:114761600-114762400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:114761600-114762600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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