Variant report

Variant	nsv887320
Chromosome Location	chr7:3110446-3134593
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:3118056-3118550	GM12878	blood:	n/a	n/a
2	ATF2	chr7:3131973-3132406	GM12878	blood:	n/a	n/a
3	ATF2	chr7:3132072-3132548	GM12878	blood:	n/a	n/a
4	ATF2	chr7:3118024-3118508	GM12878	blood:	n/a	n/a
5	BATF	chr7:3118166-3118517	GM12878	blood:	n/a	n/a
6	BATF	chr7:3132066-3132400	GM12878	blood:	n/a	n/a
7	BATF	chr7:3114599-3114890	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:3118127-3118458	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:3118124-3118494	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:3118138-3118639	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:3118443-3118622	K562	blood:	n/a	n/a
12	BHLHE40	chr7:3126085-3126131	K562	blood:	n/a	n/a
13	BHLHE40	chr7:3120025-3120105	K562	blood:	n/a	n/a
14	BHLHE40	chr7:3132108-3132440	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:3122367-3122715	K562	blood:	n/a	chr7:3122437-3122446
16	CEBPB	chr7:3116334-3116728	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:3115156-3115502	HepG2	liver:	n/a	chr7:3115311-3115322
18	CEBPB	chr7:3115180-3115481	A549	lung:	n/a	chr7:3115311-3115322
19	CEBPB	chr7:3115199-3115474	IMR90	lung:	n/a	chr7:3115311-3115322
20	CEBPB	chr7:3116404-3116590	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:3115189-3115491	K562	blood:	n/a	chr7:3115311-3115322
22	CEBPB	chr7:3115188-3115472	Hela-S3	cervix:	n/a	chr7:3115311-3115322
23	CHD2	chr7:3117626-3117667	HepG2	liver:	n/a	n/a
24	CHD2	chr7:3118168-3118456	GM12878	blood:	n/a	n/a
25	CREB1	chr7:3118037-3118644	GM12878	blood:	n/a	n/a
26	CREB1	chr7:3132031-3132499	GM12878	blood:	n/a	chr7:3132241-3132254
27	CREB1	chr7:3131965-3132570	GM12878	blood:	n/a	chr7:3132241-3132254
28	CREB1	chr7:3117968-3118642	GM12878	blood:	n/a	n/a
29	CTCF	chr7:3129187-3129443	Gliobla	brain:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
30	CTCF	chr7:3129260-3129410	BJ	skin:	n/a	chr7:3129314-3129323
31	CTCF	chr7:3129180-3129447	MCF-7	breast:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
32	CTCF	chr7:3129240-3129390	RPTEC	kidney:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
33	CTCF	chr7:3129178-3129439	GM19240	blood:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
34	CTCF	chr7:3129240-3129390	WERI-Rb-1	eye:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
35	CTCF	chr7:3128956-3129069	GM19238	blood:	n/a	n/a
36	CTCF	chr7:3128924-3129705	SK-N-SH	brain:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
37	CTCF	chr7:3129220-3129370	HMEC	breast:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
38	CTCF	chr7:3129171-3129439	K562	blood:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
39	CTCF	chr7:3132320-3132470	HBMEC	blood vessel:	n/a	chr7:3132354-3132367
40	CTCF	chr7:3129020-3129170	NHEK	skin:	n/a	n/a
41	CTCF	chr7:3129001-3129060	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:3129220-3129370	Hela-S3	cervix:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
43	CTCF	chr7:3129240-3129390	SK-N-SH_RA	brain:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
44	CTCF	chr7:3129253-3129400	LNCaP	prostate:	n/a	chr7:3129314-3129323
45	CTCF	chr7:3129180-3129330	GM12872	blood:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
46	CTCF	chr7:3129240-3129390	GM12866	blood:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
47	CTCF	chr7:3129058-3129597	MCF-7	breast:	n/a	chr7:3129314-3129323 chr7:3129415-3129423 chr7:3129243-3129252
48	CTCF	chr7:3128950-3129094	GM12891	blood:	n/a	n/a
49	CTCF	chr7:3129220-3129370	HEK293	kidney:	n/a	chr7:3129314-3129323 chr7:3129243-3129252
50	CTCF	chr7:3129220-3129370	HCPEpiC	choroid plexus:	n/a	chr7:3129314-3129323 chr7:3129243-3129252

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3127028-3127078	HRCEpiC	kidney:	n/a
2	chr7:3127028-3127078	HRCEpiC	kidney:	n/a
3	chr7:3127028-3127078	A549	lung:	n/a
4	chr7:3134557-3134607	ProgFib	skin:	n/a
5	chr7:3134557-3134607	H1-hESC	embryonic stem cell:	embryo
6	chr7:3127028-3127078	SK-N-SH	brain:	n/a
7	chr7:3134557-3134607	AG04449	skin:	fetal
8	chr7:3134592-3134642	NT2-D1	testis:	n/a
9	chr7:3127028-3127078	AoSMC	blood vessel:	n/a
10	chr7:3134557-3134607	PANC-1	pancreas:	n/a
11	chr7:3127028-3127078	SAEC	small airway:	n/a
12	chr7:3127028-3127078	GM12878	blood:	n/a
13	chr7:3134557-3134607	AG09319	gingival:	n/a
14	chr7:3127028-3127078	HCM	heart:	n/a
15	chr7:3134557-3134607	HUVEC	blood vessel:	n/a
16	chr7:3127028-3127078	AG09309	skin:	n/a
17	chr7:3134592-3134642	BJ	skin:	n/a
18	chr7:3134557-3134607	HEEpiC	esophagus:	n/a
19	chr7:3134557-3134607	Hela-S3	cervix:	n/a
20	chr7:3134557-3134607	SK-N-SH_RA	brain:	n/a
21	chr7:3134557-3134607	HL-60	blood:	n/a
22	chr7:3127028-3127078	AG09319	gingival:	n/a
23	chr7:3127028-3127078	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:3134557-3134607	SK-N-SH	brain:	n/a
25	chr7:3127028-3127078	U87	brain:	n/a
26	chr7:3134557-3134607	LNCaP	prostate:	n/a
27	chr7:3134592-3134642	GM19239	blood:	n/a
28	chr7:3134592-3134642	CMK	blood:	n/a
29	chr7:3127028-3127078	HCT-116	colon:	n/a
30	chr7:3134592-3134642	HMEC	breast:	n/a
31	chr7:3134557-3134607	Caco-2	colon:	n/a
32	chr7:3134592-3134642	NB4	blood:	n/a
33	chr7:3127028-3127078	BJ	skin:	n/a
34	chr7:3127028-3127078	HRPEpiC	eye:	n/a
35	chr7:3134592-3134642	NHBE	bronchial:	n/a
36	chr7:3134592-3134642	Jurkat	blood:	n/a
37	chr7:3134592-3134642	HCF	heart:	n/a
38	chr7:3134592-3134642	AoSMC	blood vessel:	n/a
39	chr7:3134557-3134607	GM19239	blood:	n/a
40	chr7:3134592-3134642	HepG2	liver:	n/a
41	chr7:3127028-3127078	K562	blood:	n/a
42	chr7:3134592-3134642	SAEC	small airway:	n/a
43	chr7:3134592-3134642	Caco-2	colon:	n/a
44	chr7:3134557-3134607	MCF10A-Er-Src	breast:	n/a
45	chr7:3127028-3127078	ECC-1	luminal epithelium:	n/a
46	chr7:3134557-3134607	HIPEpiC	eye:	n/a
47	chr7:3127028-3127078	HepG2	liver:	n/a
48	chr7:3134557-3134607	HCF	heart:	n/a
49	chr7:3134592-3134642	HAEpiC	amniotic membrane:	n/a
50	chr7:3134592-3134642	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:2913908..2916162-chr7:3122594..3124369,2	MCF-7	breast:
2	chr7:2926599..2927259-chr7:3129024..3129578,2	MCF-7	breast:
3	chr7:3095854..3098003-chr7:3113268..3116037,2	K562	blood:
4	chr7:3128837..3129871-chr7:3239803..3240577,4	MCF-7	breast:
5	chr7:3113104..3115838-chr7:3115974..3117943,2	K562	blood:
6	chr7:2913414..2914953-chr7:3113951..3116529,2	MCF-7	breast:
7	chr7:3114729..3116313-chr7:3116448..3118369,2	MCF-7	breast:
8	chr7:3113104..3115838-chr7:3115974..3117943,2	K562	blood:
9	chr7:3114729..3116313-chr7:3116448..3118369,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC091801.1.1-5	chr7:3133765-3135219	XLOC_006338
2	lnc-CARD11-1	chr7:3122886-3123252	XLOC_006337
3	lnc-AC091801.1.1-5	chr7:3133765-3135219	XLOC_006338
4	lnc-CARD11-3	chr7:3124135-3124176	l_3354_chr7:3100290-3107234_whiteBloodCell
5	lnc-CARD11-1	chr7:3125986-3126055	XLOC_006337

Variant related genes	Relation type
ENSG00000228334	TF binding region
ENSG00000228334	CpG island
PLIN3	miRNA target sites

Extended variants
information (count: 1202 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13223548	chr7:3110446-3110447	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs57844578	chr7:3110468-3110469	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs372783577	chr7:3110472-3110473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531195624	chr7:3110536-3110537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551104972	chr7:3110556-3110557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571255529	chr7:3110575-3110576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs13234017	chr7:3110587-3110588	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs12700542	chr7:3110620-3110621	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs78723777	chr7:3110621-3110622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536577506	chr7:3110622-3110623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556481503	chr7:3110628-3110629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12700543	chr7:3110653-3110654	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs544614277	chr7:3110671-3110672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76712661	chr7:3110685-3110686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75401659	chr7:3110689-3110690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142135220	chr7:3110735-3110736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143715455	chr7:3110760-3110761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529471134	chr7:3110784-3110785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369813199	chr7:3110786-3110787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144876639	chr7:3110787-3110788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184970526	chr7:3110842-3110843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146758905	chr7:3110905-3110906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531836503	chr7:3110918-3110919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2396960	chr7:3110933-3110934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs141891358	chr7:3111015-3111016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs150201942	chr7:3111022-3111023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs57454085	chr7:3111026-3111027	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs547446589	chr7:3111027-3111028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2396959	chr7:3111043-3111044	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs538545683	chr7:3111067-3111068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75854839	chr7:3111126-3111127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556544972	chr7:3111218-3111219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569970848	chr7:3111260-3111261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs6978715	chr7:3111292-3111293	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs75622463	chr7:3111341-3111342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189422927	chr7:3111343-3111344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79429496	chr7:3111353-3111354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138801068	chr7:3111363-3111364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73298805	chr7:3111389-3111390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142266261	chr7:3111424-3111425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562701152	chr7:3111426-3111427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs59608562	chr7:3111427-3111428	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545653122	chr7:3111441-3111442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564755879	chr7:3111467-3111468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186075130	chr7:3111480-3111481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6964346	chr7:3111491-3111492	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs572153457	chr7:3111535-3111536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs6968442	chr7:3111536-3111537	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529768527	chr7:3111562-3111563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550012022	chr7:3111565-3111566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3102000-3113800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr7:3103200-3110800	Enhancers	Primary T cells fromperipheralblood	blood
3	chr7:3103200-3111000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr7:3105800-3113600	Weak transcription	Aorta	Aorta
5	chr7:3108800-3111600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:3109800-3111000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr7:3110000-3110800	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr7:3110800-3111800	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr7:3111600-3111800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
10	chr7:3111800-3112400	Enhancers	Primary T cells fromperipheralblood	blood
11	chr7:3113200-3113600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:3113200-3113600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr7:3113400-3114200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr7:3113600-3113800	ZNF genes & repeats	Aorta	Aorta
15	chr7:3113600-3113800	Enhancers	Fetal Stomach	stomach
16	chr7:3113600-3114000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:3113600-3114600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:3114200-3114400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:3114200-3114600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr7:3114400-3114600	Enhancers	Fetal Stomach	stomach
21	chr7:3116200-3117000	Enhancers	HepG2	liver
22	chr7:3116800-3117200	Enhancers	Fetal Intestine Large	intestine
23	chr7:3117600-3119000	Enhancers	Primary B cells from peripheral blood	blood
24	chr7:3118000-3118400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:3118000-3118600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:3118400-3119000	Enhancers	GM12878-XiMat	blood
27	chr7:3118400-3122400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:3119000-3121800	Weak transcription	Primary B cells from peripheral blood	blood
29	chr7:3121600-3123600	Enhancers	Adipose Nuclei	Adipose
30	chr7:3121800-3123000	Enhancers	Primary B cells from peripheral blood	blood
31	chr7:3122000-3123600	Enhancers	Placenta	Placenta
32	chr7:3122200-3122600	Enhancers	Primary T cells fromperipheralblood	blood
33	chr7:3122200-3122800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr7:3122400-3122800	Enhancers	Primary B cells from cord blood	blood
35	chr7:3122600-3123200	Enhancers	Aorta	Aorta
36	chr7:3123000-3124200	Enhancers	Fetal Brain Male	brain
37	chr7:3123000-3130200	Weak transcription	Primary B cells from peripheral blood	blood
38	chr7:3123200-3126400	Weak transcription	Aorta	Aorta
39	chr7:3125000-3126600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:3126200-3126800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr7:3126400-3126800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr7:3126400-3127000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:3126400-3127000	Bivalent Enhancer	Placenta	Placenta
44	chr7:3126400-3127400	Enhancers	Aorta	Aorta
45	chr7:3126600-3126800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:3126600-3127400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:3126600-3127400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr7:3126600-3127400	Bivalent Enhancer	Fetal Stomach	stomach
49	chr7:3126600-3128000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:3126800-3127400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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