Variant report

Variant	esv2762347
Chromosome Location	chr3:137851198-137910007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1274)
CpG islands
(count:1955)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1274 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:137899485-137899803	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:137905839-137906287	K562	blood:	n/a	n/a
3	ARID3A	chr3:137899379-137899843	K562	blood:	n/a	n/a
4	ARID3A	chr3:137879784-137879972	K562	blood:	n/a	n/a
5	ARID3A	chr3:137905658-137906424	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:137893562-137894000	HepG2	liver:	n/a	n/a
7	ATF2	chr3:137893446-137893845	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:137905958-137906570	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:137905995-137906423	GM12878	blood:	n/a	n/a
10	ATF2	chr3:137893571-137893865	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr3:137906031-137906379	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr3:137893293-137893967	GM12878	blood:	n/a	n/a
13	ATF2	chr3:137893467-137893965	GM12878	blood:	n/a	n/a
14	ATF3	chr3:137906066-137906469	A549	lung:	n/a	n/a
15	BCLAF1	chr3:137893329-137893921	GM12878	blood:	n/a	chr3:137893773-137893782 chr3:137893770-137893779
16	BHLHE40	chr3:137905720-137906807	GM12878	blood:	n/a	chr3:137906649-137906665
17	BHLHE40	chr3:137905804-137906451	K562	blood:	n/a	n/a
18	BHLHE40	chr3:137893040-137893866	K562	blood:	n/a	n/a
19	BRCA1	chr3:137906134-137906371	HepG2	liver:	n/a	n/a
20	BRCA1	chr3:137906113-137906326	GM12878	blood:	n/a	n/a
21	BRCA1	chr3:137893207-137893999	H1-hESC	embryonic stem cell:	n/a	chr3:137893790-137893799
22	BRCA1	chr3:137906931-137907058	HepG2	liver:	n/a	n/a
23	BRCA1	chr3:137893194-137894057	Hela-S3	cervix:	n/a	chr3:137893790-137893799
24	BRCA1	chr3:137893441-137893994	GM12878	blood:	n/a	chr3:137893790-137893799
25	BRCA1	chr3:137906673-137906706	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr3:137905720-137906355	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr3:137893480-137893968	HepG2	liver:	n/a	chr3:137893790-137893799
28	CBX3	chr3:137906024-137906469	K562	blood:	n/a	n/a
29	CBX3	chr3:137906814-137907191	K562	blood:	n/a	n/a
30	CBX3	chr3:137893430-137893900	K562	blood:	n/a	n/a
31	CCNT2	chr3:137893163-137893776	K562	blood:	n/a	n/a
32	CCNT2	chr3:137905901-137906954	K562	blood:	n/a	n/a
33	CEBPB	chr3:137856928-137856955	H1-hESC	embryonic stem cell:	n/a	chr3:137856932-137856943
34	CEBPB	chr3:137893158-137893878	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr3:137905683-137906578	GM12878	blood:	n/a	n/a
36	CEBPB	chr3:137906829-137907178	K562	blood:	n/a	n/a
37	CEBPB	chr3:137905188-137907503	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:137906076-137907416	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:137856793-137857016	K562	blood:	n/a	chr3:137856932-137856943
40	CEBPB	chr3:137856876-137857091	HepG2	liver:	n/a	chr3:137856932-137856943
41	CEBPB	chr3:137893582-137893841	K562	blood:	n/a	n/a
42	CEBPB	chr3:137905783-137906499	K562	blood:	n/a	n/a
43	CEBPB	chr3:137906112-137906453	K562	blood:	n/a	n/a
44	CEBPB	chr3:137870257-137870422	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr3:137906164-137906502	HepG2	liver:	n/a	n/a
46	CEBPD	chr3:137905952-137906579	HepG2	liver:	n/a	n/a
47	CEBPD	chr3:137893562-137893803	HepG2	liver:	n/a	n/a
48	CHD1	chr3:137906174-137907097	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr3:137905917-137907007	GM12878	blood:	n/a	n/a
50	CHD1	chr3:137893475-137893895	GM12878	blood:	n/a	chr3:137893790-137893799

(count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:137893432-137893482	NHBE	bronchial:	n/a
2	chr3:137893807-137893857	HCPEpiC	choroid plexus:	n/a
3	chr3:137893707-137893757	HRCEpiC	kidney:	n/a
4	chr3:137893432-137893482	NHBE	bronchial:	n/a
5	chr3:137893807-137893857	HCPEpiC	choroid plexus:	n/a
6	chr3:137893707-137893757	HRCEpiC	kidney:	n/a
7	chr3:137902226-137902276	U87	brain:	n/a
8	chr3:137851874-137851924	HCPEpiC	choroid plexus:	n/a
9	chr3:137905836-137905886	AG10803	skin:	n/a
10	chr3:137906213-137906263	AG09309	skin:	n/a
11	chr3:137906066-137906116	ECC-1	luminal epithelium:	n/a
12	chr3:137893270-137893320	CMK	blood:	n/a
13	chr3:137905908-137905958	ECC-1	luminal epithelium:	n/a
14	chr3:137893793-137893843	A549	lung:	n/a
15	chr3:137907359-137907409	NB4	blood:	n/a
16	chr3:137906066-137906116	Caco-2	colon:	n/a
17	chr3:137893743-137893793	HNPCEpiC	eye:	n/a
18	chr3:137893432-137893482	GM12892	blood:	n/a
19	chr3:137893807-137893857	NT2-D1	testis:	n/a
20	chr3:137896703-137896753	AG04450	lung:	fetal
21	chr3:137906213-137906263	GM12891	blood:	n/a
22	chr3:137904059-137904109	HCPEpiC	choroid plexus:	n/a
23	chr3:137906342-137906392	AG10803	skin:	n/a
24	chr3:137893718-137893768	HCPEpiC	choroid plexus:	n/a
25	chr3:137851776-137851826	Hepatocyte	liver:	n/a
26	chr3:137893432-137893482	HCT-116	colon:	n/a
27	chr3:137880405-137880455	NHBE	bronchial:	n/a
28	chr3:137893795-137893845	GM12892	blood:	n/a
29	chr3:137893743-137893793	ovcar-3	ovarian:	n/a
30	chr3:137906050-137906100	SKMC	muscle:	n/a
31	chr3:137906066-137906116	NB4	blood:	n/a
32	chr3:137905836-137905886	HCPEpiC	choroid plexus:	n/a
33	chr3:137893743-137893793	HAEpiC	amniotic membrane:	n/a
34	chr3:137906050-137906100	SK-N-SH	brain:	n/a
35	chr3:137905877-137905927	GM12892	blood:	n/a
36	chr3:137906106-137906156	AoSMC	blood vessel:	n/a
37	chr3:137906122-137906172	SK-N-SH_RA	brain:	n/a
38	chr3:137904059-137904109	HRE	kidney:	n/a
39	chr3:137893793-137893843	H1-hESC	embryonic stem cell:	embryo
40	chr3:137893795-137893845	MCF-7	breast:	n/a
41	chr3:137893270-137893320	HUVEC	blood vessel:	n/a
42	chr3:137906122-137906172	HIPEpiC	eye:	n/a
43	chr3:137893699-137893749	HNPCEpiC	eye:	n/a
44	chr3:137893743-137893793	NHBE	bronchial:	n/a
45	chr3:137907359-137907409	GM06990	blood:	n/a
46	chr3:137893793-137893843	MCF10A-Er-Src	breast:	n/a
47	chr3:137893707-137893757	HEEpiC	esophagus:	n/a
48	chr3:137880405-137880455	HUVEC	blood vessel:	n/a
49	chr3:137852643-137852693	HRCEpiC	kidney:	n/a
50	chr3:137906213-137906263	HRCEpiC	kidney:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:137903312..137904852-chr3:137905102..137906663,2	MCF-7	breast:
2	chr3:137881624..137884175-chr3:137906260..137908266,2	K562	blood:
3	chr3:137889024..137895470-chr3:137896789..137909029,20	K562	blood:
4	chr3:137884117..137886892-chr3:137892059..137895192,4	MCF-7	breast:
5	chr3:137904054..137908081-chr3:137908152..137912895,9	MCF-7	breast:
6	chr3:137900435..137902398-chr3:137902812..137904921,3	MCF-7	breast:
7	chr3:137886831..137889981-chr3:137890698..137894994,6	MCF-7	breast:
8	chr3:137883514..137885289-chr3:137888443..137890790,3	MCF-7	breast:
9	chr17:56708248..56710673-chr3:137893303..137894884,2	MCF-7	breast:
10	chr3:137904820..137906747-chr3:137954562..137956605,2	K562	blood:
11	chr3:137881624..137884175-chr3:137906260..137908266,2	K562	blood:
12	chr3:137908958..137910626-chr3:138333368..138336043,2	K562	blood:
13	chr3:137891675..137895635-chr3:137902725..137910565,16	MCF-7	breast:
14	chr3:137904811..137907736-chr3:137908254..137910507,2	K562	blood:
15	chr12:3068006..3068677-chr3:137906028..137906625,2	Hela-S3	cervix:
16	chr3:137889293..137890860-chr3:137969954..137972677,2	K562	blood:
17	chr3:137892183..137893942-chr3:138313140..138314743,2	K562	blood:
18	chr3:137880343..137882012-chr3:137893517..137895073,2	K562	blood:
19	chr3:137819951..137820556-chr3:137867215..137868064,2	MCF-7	breast:
20	chr3:137891568..137893180-chr3:137920750..137922415,2	K562	blood:
21	chr3:137889024..137895470-chr3:137896789..137909029,20	K562	blood:
22	chr3:137899229..137899796-chr3:138067137..138067658,2	MCF-7	breast:
23	chr3:137876601..137878547-chr3:137880308..137882922,2	MCF-7	breast:
24	chr3:137893238..137894030-chr6:88411539..88412391,2	Hela-S3	cervix:
25	chr3:137882800..137885689-chr3:137905079..137908377,3	MCF-7	breast:
26	chr3:137900693..137902461-chr3:138048326..138049847,2	MCF-7	breast:
27	chr3:137860771..137863892-chr3:137892131..137894669,3	MCF-7	breast:
28	chr3:137883514..137885289-chr3:137888443..137890790,3	MCF-7	breast:
29	chr3:137891492..137895416-chr3:137896439..137900714,7	MCF-7	breast:
30	chr3:137904685..137906516-chr3:137939797..137942288,3	K562	blood:
31	chr3:137900435..137902398-chr3:137902812..137904921,3	MCF-7	breast:
32	chr3:137898900..137900113-chr3:138003497..138004427,6	MCF-7	breast:
33	chr3:137880775..137882783-chr3:137887476..137889731,2	K562	blood:
34	chr3:137881170..137883124-chr3:137906116..137908266,2	K562	blood:
35	chr3:137882946..137886396-chr3:137891072..137895118,4	MCF-7	breast:
36	chr3:137890311..137895409-chr3:137904718..137908692,8	MCF-7	breast:
37	chr3:137890311..137895409-chr3:137904718..137908692,8	MCF-7	breast:
38	chr3:137891989..137894675-chr3:137980214..137982632,2	K562	blood:
39	chr3:137906774..137910394-chr3:137911786..137917069,7	K562	blood:
40	chr3:137846713..137849373-chr3:137854180..137855933,2	K562	blood:
41	chr3:137899186..137900054-chr3:137981994..137982584,2	MCF-7	breast:
42	chr3:137908519..137910885-chr3:137962285..137965162,2	K562	blood:
43	chr3:137886740..137888372-chr3:137892285..137893890,2	K562	blood:
44	chr3:137881170..137883124-chr3:137906116..137908266,2	K562	blood:
45	chr10:13344143..13344643-chr3:137893316..137893818,2	Hela-S3	cervix:
46	chr3:137898654..137900353-chr3:137922615..137924973,2	MCF-7	breast:
47	chr3:63810836..63811646-chr3:137862140..137863107,2	MCF-7	breast:
48	chr3:137892199..137894619-chr3:137909781..137912615,2	K562	blood:
49	chr3:137876601..137878547-chr3:137880308..137882922,2	MCF-7	breast:
50	chr3:137882800..137885689-chr3:137905079..137908377,3	MCF-7	breast:

No data

Variant related genes	Relation type
A4GNT	TF binding region
ARMC8	TF binding region
DBR1	TF binding region
A4GNT	CpG island
ARMC8	CpG island
DBR1	CpG island
ENSG00000114107	chromatin interactions
ENSG00000135334	chromatin interactions
ENSG00000138231	chromatin interactions
ENSG00000107537	chromatin interactions
ENSG00000181322	chromatin interactions
ENSG00000114098	chromatin interactions
ENSG00000197905	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000158186	chromatin interactions

Extended variants
information (count: 1574 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1574 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2724692	chr3:137851198-137851199	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188161164	chr3:137851227-137851228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35585241	chr3:137851270-137851271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149461058	chr3:137851300-137851301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567740661	chr3:137851320-137851321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572881400	chr3:137851331-137851332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192372100	chr3:137851350-137851351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75568477	chr3:137851353-137851354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536829203	chr3:137851358-137851359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145881251	chr3:137851379-137851380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576057576	chr3:137851389-137851390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542345190	chr3:137851482-137851483	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs555595117	chr3:137851608-137851609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184681791	chr3:137851658-137851659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558283611	chr3:137851718-137851719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571986627	chr3:137851726-137851727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189548392	chr3:137851755-137851756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540974967	chr3:137851758-137851759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560841331	chr3:137851777-137851778	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs111596177	chr3:137851798-137851799	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs73867017	chr3:137851874-137851875	Weak transcription Enhancers ZNF genes & repeats	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs114639550	chr3:137851879-137851880	Weak transcription Enhancers ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs181560789	chr3:137851898-137851899	Weak transcription Enhancers ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs531730425	chr3:137851963-137851964	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs372166415	chr3:137851966-137851967	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs185799739	chr3:137851983-137851984	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs565161254	chr3:137852000-137852001	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs376759164	chr3:137852010-137852011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575666757	chr3:137852065-137852066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113198783	chr3:137852086-137852087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75405051	chr3:137852148-137852149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142952049	chr3:137852212-137852213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544079425	chr3:137852249-137852250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550417903	chr3:137852252-137852253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs62280645	chr3:137852291-137852292	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs111375930	chr3:137852307-137852308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146135236	chr3:137852322-137852323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565581469	chr3:137852340-137852341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189042035	chr3:137852405-137852406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148772591	chr3:137852452-137852453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574416371	chr3:137852463-137852464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181788977	chr3:137852556-137852557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556913049	chr3:137852575-137852576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369574798	chr3:137852579-137852580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372609109	chr3:137852630-137852631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76266180	chr3:137852643-137852644	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs545215161	chr3:137852735-137852736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186327039	chr3:137852738-137852739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533279657	chr3:137852767-137852768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141444411	chr3:137852775-137852776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:137843800-137851800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:137845200-137853200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr3:137847800-137851200	Active TSS	Fetal Stomach	stomach
4	chr3:137850000-137851800	Weak transcription	Pancreas	Pancrea
5	chr3:137850600-137856800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:137851000-137851200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:137851000-137851200	Enhancers	Fetal Intestine Small	intestine
8	chr3:137851000-137852400	Enhancers	Stomach Mucosa	stomach
9	chr3:137851200-137851600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:137851200-137852200	Weak transcription	Fetal Intestine Small	intestine
11	chr3:137851600-137852000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr3:137851800-137852000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:137851800-137852600	Enhancers	Gastric	stomach
14	chr3:137851800-137854000	Enhancers	Pancreas	Pancrea
15	chr3:137852000-137852200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:137852200-137852800	Enhancers	Fetal Intestine Small	intestine
17	chr3:137852200-137859400	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr3:137852400-137853200	Weak transcription	Stomach Mucosa	stomach
19	chr3:137852400-137853400	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr3:137852600-137856600	Weak transcription	Gastric	stomach
21	chr3:137852800-137853200	Weak transcription	Fetal Intestine Small	intestine
22	chr3:137853200-137853800	Enhancers	Adipose Nuclei	Adipose
23	chr3:137853200-137853800	Enhancers	Fetal Intestine Small	intestine
24	chr3:137853200-137853800	Enhancers	Stomach Mucosa	stomach
25	chr3:137853200-137854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr3:137853200-137856200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr3:137853400-137855000	Enhancers	Primary B cells from peripheral blood	blood
28	chr3:137853400-137855200	Enhancers	Brain Hippocampus Middle	brain
29	chr3:137853400-137857000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr3:137853400-137857600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr3:137853400-137857800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr3:137853600-137855200	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr3:137853600-137857000	Enhancers	Primary hematopoietic stem cells	blood
34	chr3:137853600-137857400	Enhancers	Primary B cells from cord blood	blood
35	chr3:137853800-137854200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:137853800-137854800	Weak transcription	Fetal Intestine Small	intestine
37	chr3:137853800-137855200	Weak transcription	Stomach Mucosa	stomach
38	chr3:137853800-137855600	Weak transcription	Adipose Nuclei	Adipose
39	chr3:137854000-137856600	Weak transcription	Pancreas	Pancrea
40	chr3:137854200-137855000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:137854200-137855000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:137854400-137855200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr3:137854400-137855400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:137854400-137855400	Enhancers	Brain Substantia Nigra	brain
45	chr3:137854600-137855000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr3:137854600-137855000	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr3:137854800-137855400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr3:137854800-137855800	Enhancers	Fetal Intestine Small	intestine
49	chr3:137855000-137855400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:137855000-137855400	Weak transcription	Primary B cells from peripheral blood	blood

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