Variant report

Variant	nsv5947
Chromosome Location	chr7:128704900-128749885
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:873)
CpG islands
(count:123)
Chromatin interactive
region (count:55)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:873 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:128742509-128743042	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:128731574-128731901	K562	blood:	n/a	n/a
3	ARID3A	chr7:128725229-128725499	K562	blood:	n/a	n/a
4	ARID3A	chr7:128740628-128741001	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:128706300-128707884	K562	blood:	n/a	n/a
6	ATF1	chr7:128706465-128707615	K562	blood:	n/a	n/a
7	ATF2	chr7:128731448-128732072	GM12878	blood:	n/a	n/a
8	ATF2	chr7:128731508-128731964	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:128729509-128730267	GM12878	blood:	n/a	n/a
10	ATF2	chr7:128735115-128735799	GM12878	blood:	n/a	n/a
11	ATF2	chr7:128733911-128734339	GM12878	blood:	n/a	n/a
12	ATF2	chr7:128735226-128735863	GM12878	blood:	n/a	n/a
13	ATF2	chr7:128729507-128730081	GM12878	blood:	n/a	n/a
14	ATF2	chr7:128733854-128734302	GM12878	blood:	n/a	n/a
15	ATF3	chr7:128731483-128731792	K562	blood:	n/a	n/a
16	ATF3	chr7:128706290-128707548	K562	blood:	n/a	n/a
17	BACH1	chr7:128706916-128707205	H1-hESC	embryonic stem cell:	n/a	chr7:128707087-128707101
18	BACH1	chr7:128706337-128706650	K562	blood:	n/a	n/a
19	BACH1	chr7:128731714-128731928	K562	blood:	n/a	n/a
20	BATF	chr7:128713809-128714071	GM12878	blood:	n/a	chr7:128713952-128713963
21	BATF	chr7:128729624-128730235	GM12878	blood:	n/a	n/a
22	BATF	chr7:128713765-128714129	GM12878	blood:	n/a	chr7:128713952-128713963
23	BATF	chr7:128729604-128729993	GM12878	blood:	n/a	n/a
24	BATF	chr7:128733915-128734291	GM12878	blood:	n/a	n/a
25	BATF	chr7:128731544-128731878	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:128733935-128734268	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:128735295-128735641	GM12878	blood:	n/a	n/a
28	BCL11A	chr7:128729620-128730027	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:128729686-128729988	GM12878	blood:	n/a	n/a
30	BCL3	chr7:128729609-128729998	GM12878	blood:	n/a	n/a
31	BCL3	chr7:128738681-128739074	GM12878	blood:	n/a	n/a
32	BCLAF1	chr7:128735186-128735704	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:128731501-128732047	GM12878	blood:	n/a	chr7:128732033-128732042
34	BCLAF1	chr7:128729491-128730234	GM12878	blood:	n/a	n/a
35	BCLAF1	chr7:128731338-128732188	GM12878	blood:	n/a	chr7:128732033-128732042
36	BCLAF1	chr7:128735076-128735817	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:128742634-128742981	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:128706256-128707208	K562	blood:	n/a	n/a
39	BHLHE40	chr7:128731545-128731904	K562	blood:	n/a	n/a
40	BHLHE40	chr7:128735257-128735595	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:128731549-128731968	GM12878	blood:	n/a	n/a
42	BRCA1	chr7:128731574-128731787	GM12878	blood:	n/a	n/a
43	BRCA1	chr7:128731556-128731874	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr7:128731559-128731753	HepG2	liver:	n/a	n/a
45	BRCA1	chr7:128705590-128705640	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr7:128731481-128731997	K562	blood:	n/a	n/a
47	CBX3	chr7:128708013-128708623	K562	blood:	n/a	n/a
48	CBX3	chr7:128706015-128707896	K562	blood:	n/a	n/a
49	CCNT2	chr7:128706388-128706958	K562	blood:	n/a	n/a
50	CCNT2	chr7:128707355-128707549	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128731386-128731436	A549	lung:	n/a
2	chr7:128731386-128731436	A549	lung:	n/a
3	chr7:128731386-128731436	HEK293	kidney:	embryo
4	chr7:128707039-128707089	Hela-S3	cervix:	n/a
5	chr7:128707039-128707089	GM12878	blood:	n/a
6	chr7:128731386-128731436	HMEC	breast:	n/a
7	chr7:128707039-128707089	AG09319	gingival:	n/a
8	chr7:128707039-128707089	ovcar-3	ovarian:	n/a
9	chr7:128731386-128731436	HUVEC	blood vessel:	n/a
10	chr7:128731386-128731436	Caco-2	colon:	n/a
11	chr7:128707039-128707089	ProgFib	skin:	n/a
12	chr7:128731386-128731436	NT2-D1	testis:	n/a
13	chr7:128707039-128707089	SK-N-SH_RA	brain:	n/a
14	chr7:128707039-128707089	HIPEpiC	eye:	n/a
15	chr7:128731386-128731436	AG04450	lung:	fetal
16	chr7:128731386-128731436	GM12891	blood:	n/a
17	chr7:128707039-128707089	IMR90	lung:	fetal
18	chr7:128731386-128731436	AoSMC	blood vessel:	n/a
19	chr7:128707039-128707089	HCT-116	colon:	n/a
20	chr7:128731386-128731436	Hela-S3	cervix:	n/a
21	chr7:128707039-128707089	GM19239	blood:	n/a
22	chr7:128707039-128707089	Jurkat	blood:	n/a
23	chr7:128731386-128731436	GM19239	blood:	n/a
24	chr7:128707039-128707089	NHBE	bronchial:	n/a
25	chr7:128707039-128707089	HUVEC	blood vessel:	n/a
26	chr7:128731386-128731436	GM06990	blood:	n/a
27	chr7:128707039-128707089	HMEC	breast:	n/a
28	chr7:128707039-128707089	ECC-1	luminal epithelium:	n/a
29	chr7:128707039-128707089	SK-N-SH	brain:	n/a
30	chr7:128707039-128707089	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:128707039-128707089	NB4	blood:	n/a
32	chr7:128707039-128707089	PFSK-1	brain:	n/a
33	chr7:128731386-128731436	HRCEpiC	kidney:	n/a
34	chr7:128731386-128731436	SK-N-MC	brain:	n/a
35	chr7:128707039-128707089	BE2_C	brain:	n/a
36	chr7:128731386-128731436	U87	brain:	n/a
37	chr7:128707039-128707089	K562	blood:	n/a
38	chr7:128731386-128731436	HNPCEpiC	eye:	n/a
39	chr7:128731386-128731436	HRE	kidney:	n/a
40	chr7:128707039-128707089	SKMC	muscle:	n/a
41	chr7:128731386-128731436	PrEC	prostate:	n/a
42	chr7:128707039-128707089	A549	lung:	n/a
43	chr7:128731386-128731436	NHDF-neo	bronchial:	n/a
44	chr7:128731386-128731436	MCF10A-Er-Src	breast:	n/a
45	chr7:128707039-128707089	HRCEpiC	kidney:	n/a
46	chr7:128707039-128707089	T-47D	breast:	n/a
47	chr7:128731386-128731436	ECC-1	luminal epithelium:	n/a
48	chr7:128707039-128707089	PrEC	prostate:	n/a
49	chr7:128707039-128707089	H1-hESC	embryonic stem cell:	embryo
50	chr7:128731386-128731436	T-47D	breast:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:128730793..128732096-chr7:128853501..128854381,4	MCF-7	breast:
2	chr7:128703442..128704954-chr7:128706819..128708761,2	K562	blood:
3	chr7:128640430..128642897-chr7:128713817..128715502,2	K562	blood:
4	chr7:128518981..128521726-chr7:128729945..128731755,3	MCF-7	breast:
5	chr20:12657875..12658607-chr7:128730473..128731030,2	MCF-7	breast:
6	chr7:128722565..128724290-chr7:128725775..128728315,2	MCF-7	breast:
7	chr7:128694148..128696169-chr7:128711107..128713909,4	K562	blood:
8	chr7:128694230..128698361-chr7:128709403..128713600,5	MCF-7	breast:
9	chr7:128481770..128482607-chr7:128731640..128732184,3	MCF-7	breast:
10	chr7:128543323..128545602-chr7:128729089..128731732,2	MCF-7	breast:
11	chr7:128576739..128579546-chr7:128728612..128731057,2	MCF-7	breast:
12	chr7:128743149..128745189-chr7:128749817..128751977,2	K562	blood:
13	chr7:128703442..128704954-chr7:128706819..128708761,2	K562	blood:
14	chr7:128695213..128698206-chr7:128720937..128723020,2	MCF-7	breast:
15	chr7:128695623..128697162-chr7:128718401..128720801,2	MCF-7	breast:
16	chr7:128731432..128731937-chr7:128803431..128804420,2	MCF-7	breast:
17	chr7:128690768..128692397-chr7:128709974..128712728,2	K562	blood:
18	chr7:128694341..128696448-chr7:128729270..128733085,3	K562	blood:
19	chr7:128722565..128724290-chr7:128725775..128728315,2	MCF-7	breast:
20	chr7:128544416..128545364-chr7:128731259..128732201,6	K562	blood:
21	chr7:128713665..128715847-chr7:128722237..128724921,2	K562	blood:
22	chr7:128690605..128692450-chr7:128738032..128740772,2	K562	blood:
23	chr7:128742671..128745529-chr7:128752826..128754792,2	K562	blood:
24	chr7:128543415..128545099-chr7:128729314..128731770,2	MCF-7	breast:
25	chr7:128695195..128696945-chr7:128706166..128708418,2	MCF-7	breast:
26	chr7:128712991..128714867-chr7:128728502..128730721,2	K562	blood:
27	chr7:128743990..128745611-chr7:128795942..128798106,2	K562	blood:
28	chr7:128731307..128732251-chr7:129284641..129285143,2	K562	blood:
29	chr7:128713665..128715847-chr7:128722237..128724921,2	K562	blood:
30	chr7:128705554..128708231-chr7:128722304..128724842,2	K562	blood:
31	chr7:128647545..128649314-chr7:128729887..128731425,2	K562	blood:
32	chr7:128693117..128696073-chr7:128715266..128718557,3	K562	blood:
33	chr7:128693199..128695947-chr7:128735340..128738177,2	MCF-7	breast:
34	chr7:128693445..128696833-chr7:128704821..128709448,12	K562	blood:
35	chr7:128731303..128732213-chr7:128850012..128851029,4	K562	blood:
36	chr7:128579925..128580797-chr7:128731314..128732147,3	K562	blood:
37	chr7:128712991..128714867-chr7:128728502..128730721,2	K562	blood:
38	chr7:128544442..128544977-chr7:128731340..128732241,2	MCF-7	breast:
39	chr7:128590811..128591653-chr7:128731640..128732378,2	K562	blood:
40	chr7:128694823..128695669-chr7:128731218..128731763,2	K562	blood:
41	chr7:128697928..128700141-chr7:128704756..128706286,2	K562	blood:
42	chr7:128706137..128708231-chr7:128723342..128724943,2	K562	blood:
43	chr7:128693215..128696602-chr7:128704853..128708545,4	MCF-7	breast:
44	chr7:128481736..128482276-chr7:128731260..128731834,2	K562	blood:
45	chr7:128742139..128744810-chr7:128757802..128759404,2	K562	blood:
46	chr7:128694170..128696582-chr7:128722394..128724608,2	MCF-7	breast:
47	chr7:128692565..128697627-chr7:128730000..128734495,6	K562	blood:
48	chr7:128729541..128731737-chr7:128775619..128778494,2	K562	blood:
49	chr7:128694755..128696750-chr7:128720943..128723217,2	K562	blood:
50	chr7:128586224..128588261-chr7:128749255..128750903,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNPO3-4	chr7:128735355-128735544	NONHSAT123286
2	lnc-TNPO3-4	chr7:128735697-128735865	NONHSAT123286

No data

Variant related genes	Relation type
ENSG00000241573	TF binding region
ENSG00000241102	TF binding region
ENSG00000242162	TF binding region
ENSG00000241573	CpG island
ENSG00000241102	CpG island
ENSG00000242162	CpG island
ENSG00000242162	chromatin interactions
ENSG00000238733	chromatin interactions
ENSG00000064419	chromatin interactions
ENSG00000230359	chromatin interactions
ENSG00000128604	chromatin interactions
ENSG00000135253	chromatin interactions
ENSG00000128602	chromatin interactions
ENSG00000240416	chromatin interactions

Extended variants
information (count: 1855 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1855 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144241019	chr7:128704925-128704926	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs532970562	chr7:128704937-128704938	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs185892236	chr7:128704939-128704940	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs148307806	chr7:128704940-128704941	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567557103	chr7:128704952-128704953	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs373026826	chr7:128704968-128704969	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs551634176	chr7:128705001-128705002	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs560225357	chr7:128705028-128705029	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs76076677	chr7:128705040-128705041	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs190560599	chr7:128705068-128705069	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568170992	chr7:128705080-128705081	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs372041907	chr7:128705103-128705104	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546846796	chr7:128705112-128705113	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs535563416	chr7:128705203-128705204	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs565972827	chr7:128705243-128705244	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs569430807	chr7:128705260-128705261	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375182614	chr7:128705288-128705289	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs113600825	chr7:128705289-128705290	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs570896189	chr7:128705348-128705349	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573471958	chr7:128705392-128705393	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs533740288	chr7:128705393-128705394	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs56385229	chr7:128705413-128705414	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs55850651	chr7:128705414-128705415	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs142018657	chr7:128705438-128705439	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs146346065	chr7:128705514-128705515	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535004323	chr7:128705561-128705562	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs79065461	chr7:128705624-128705625	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562475924	chr7:128705666-128705667	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs116151169	chr7:128705694-128705695	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs139294369	chr7:128705730-128705731	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs578144691	chr7:128705757-128705758	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs560369226	chr7:128705767-128705768	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs183806110	chr7:128705833-128705834	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs546549828	chr7:128705883-128705884	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs561738935	chr7:128705905-128705906	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538375816	chr7:128705910-128705911	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs144102969	chr7:128705957-128705958	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs551032050	chr7:128705979-128705980	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs569285739	chr7:128705988-128705989	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs557286514	chr7:128705989-128705990	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs551703133	chr7:128706000-128706001	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs567104703	chr7:128706002-128706003	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs534502873	chr7:128706022-128706023	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs73228772	chr7:128706037-128706038	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs567251527	chr7:128706062-128706063	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs537877914	chr7:128706073-128706074	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs556191781	chr7:128706122-128706123	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs577687672	chr7:128706142-128706143	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs188645121	chr7:128706189-128706190	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs553695427	chr7:128706193-128706194	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128695800-128706200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:128696200-128706400	Weak transcription	Right Atrium	heart
3	chr7:128696600-128706200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:128703200-128706800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:128703800-128705800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:128704600-128705200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr7:128704600-128705800	Enhancers	Fetal Intestine Large	intestine
8	chr7:128704800-128705600	Enhancers	GM12878-XiMat	blood
9	chr7:128704800-128706000	Enhancers	K562	blood
10	chr7:128705200-128705400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:128705200-128705600	Enhancers	Fetal Intestine Small	intestine
12	chr7:128705200-128708600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr7:128705400-128706400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:128705600-128706600	Weak transcription	Fetal Intestine Small	intestine
15	chr7:128705600-128706800	Weak transcription	GM12878-XiMat	blood
16	chr7:128705800-128706200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:128705800-128706200	Weak transcription	Fetal Intestine Large	intestine
18	chr7:128706000-128707400	Enhancers	Placenta	Placenta
19	chr7:128706000-128708000	Flanking Active TSS	K562	blood
20	chr7:128706000-128709600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr7:128706200-128706400	Enhancers	H9 Cell Line	embryonic stem cell
22	chr7:128706200-128706400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:128706200-128706600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr7:128706200-128706800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr7:128706200-128706800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:128706200-128706800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr7:128706200-128707000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:128706200-128707000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:128706200-128707200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr7:128706200-128707200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr7:128706200-128707200	Enhancers	Fetal Intestine Large	intestine
32	chr7:128706200-128707200	Enhancers	Hela-S3	cervix
33	chr7:128706200-128707800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr7:128706200-128708000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:128706200-128708200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr7:128706200-128710200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr7:128706400-128706600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr7:128706400-128706800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr7:128706400-128707000	Enhancers	H1 Cell Line	embryonic stem cell
40	chr7:128706400-128707000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:128706400-128707000	Enhancers	Brain Germinal Matrix	brain
42	chr7:128706400-128707200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr7:128706400-128707200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:128706400-128707200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:128706400-128707200	Enhancers	Psoas Muscle	Psoas
46	chr7:128706400-128707200	Strong transcription	Right Atrium	heart
47	chr7:128706400-128707200	Enhancers	A549	lung
48	chr7:128706400-128707200	Enhancers	NH-A	brain
49	chr7:128706400-128707400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:128706400-128707400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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