Variant report

Variant	nsv873794
Chromosome Location	chr2:33936701-34103546
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	BACH1	chr2:33989933-33989937	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:33992471-33992698	GM12878	blood:	n/a	n/a
3	BATF	chr2:33992376-33992627	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:33992459-33992730	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:33992452-33992619	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:33992456-33992639	HepG2	liver:	n/a	n/a
7	BHLHE40	chr2:33954808-33954914	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:34010355-34011098	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:34009927-34010076	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:33950219-33950224	GM12878	blood:	n/a	n/a
11	CBX3	chr2:33986046-33986247	K562	blood:	n/a	n/a
12	CEBPB	chr2:34027732-34028058	A549	lung:	n/a	n/a
13	CEBPB	chr2:34016763-34016978	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:34050115-34050323	HepG2	liver:	n/a	chr2:34050219-34050230
15	CEBPB	chr2:34074371-34074506	H1-hESC	embryonic stem cell:	n/a	chr2:34074408-34074419
16	CEBPB	chr2:34046847-34047396	IMR90	lung:	n/a	chr2:34046985-34046996 chr2:34046985-34046998
17	CEBPB	chr2:33944249-33944412	MCF-7	breast:	n/a	chr2:33944333-33944350 chr2:33944334-33944347 chr2:33944335-33944346
18	CEBPB	chr2:33944156-33944508	HepG2	liver:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
19	CEBPB	chr2:34093496-34093707	A549	lung:	n/a	n/a
20	CEBPB	chr2:34046885-34047345	A549	lung:	n/a	chr2:34046985-34046996 chr2:34046985-34046998
21	CEBPB	chr2:34073519-34074040	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:33944200-33944431	H1-hESC	embryonic stem cell:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
23	CEBPB	chr2:34016775-34017034	A549	lung:	n/a	n/a
24	CEBPB	chr2:34016725-34017098	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:34063261-34063570	HepG2	liver:	n/a	chr2:34063436-34063447
26	CEBPB	chr2:33944196-33944468	K562	blood:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
27	CEBPB	chr2:34050108-34050338	A549	lung:	n/a	chr2:34050219-34050230
28	CEBPB	chr2:34074255-34074588	HepG2	liver:	n/a	chr2:34074408-34074419
29	CEBPB	chr2:34090949-34090976	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr2:33944156-33944511	IMR90	lung:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
31	CEBPB	chr2:34074263-34074579	A549	lung:	n/a	chr2:34074408-34074419
32	CEBPB	chr2:34016736-34017067	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr2:34027728-34028064	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:34062064-34062078	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:33944152-33944511	A549	lung:	n/a	chr2:33944333-33944350 chr2:33944409-33944421 chr2:33944334-33944347 chr2:33944335-33944346
36	CEBPB	chr2:34074246-34074592	IMR90	lung:	n/a	chr2:34074408-34074419
37	CEBPB	chr2:34047164-34047373	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:34062049-34062067	A549	lung:	n/a	n/a
39	CEBPB	chr2:34063300-34063564	IMR90	lung:	n/a	chr2:34063436-34063447
40	CEBPB	chr2:33956627-33956689	K562	blood:	n/a	n/a
41	CEBPB	chr2:34098418-34098628	A549	lung:	n/a	n/a
42	CEBPB	chr2:34046826-34047351	HepG2	liver:	n/a	chr2:34046985-34046996 chr2:34046985-34046998
43	CEBPD	chr2:33992469-33992658	K562	blood:	n/a	n/a
44	CHD2	chr2:34010971-34011007	GM12878	blood:	n/a	n/a
45	CHD2	chr2:34010211-34010613	GM12878	blood:	n/a	n/a
46	CTCF	chr2:34045911-34046001	MCF-7	breast:	n/a	chr2:34045928-34045946
47	CTCF	chr2:34008020-34008170	GM12874	blood:	n/a	chr2:34008113-34008131
48	CTCF	chr2:34008080-34008230	AG09309	skin:	n/a	chr2:34008113-34008131
49	CTCF	chr2:33990260-33990410	GM12873	blood:	n/a	n/a
50	CTCF	chr2:34008080-34008230	WERI-Rb-1	eye:	n/a	chr2:34008113-34008131

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33954347-33954397	BJ	skin:	n/a
2	chr2:33954347-33954397	BJ	skin:	n/a
3	chr2:33953195-33953245	T-47D	breast:	n/a
4	chr2:33954347-33954397	SK-N-MC	brain:	n/a
5	chr2:33953195-33953245	GM06990	blood:	n/a
6	chr2:33953437-33953487	ECC-1	luminal epithelium:	n/a
7	chr2:33952488-33952538	ECC-1	luminal epithelium:	n/a
8	chr2:33948457-33948507	Caco-2	colon:	n/a
9	chr2:33948457-33948507	HEEpiC	esophagus:	n/a
10	chr2:33953195-33953245	A549	lung:	n/a
11	chr2:33953203-33953253	SAEC	small airway:	n/a
12	chr2:33953195-33953245	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:33948457-33948507	NB4	blood:	n/a
14	chr2:33953203-33953253	PrEC	prostate:	n/a
15	chr2:33952673-33952723	GM12892	blood:	n/a
16	chr2:33954043-33954093	BE2_C	brain:	n/a
17	chr2:33954735-33954785	RPTEC	kidney:	n/a
18	chr2:33952423-33952473	AG10803	skin:	n/a
19	chr2:33954043-33954093	HMEC	breast:	n/a
20	chr2:33954735-33954785	ProgFib	skin:	n/a
21	chr2:33953370-33953420	HIPEpiC	eye:	n/a
22	chr2:33952673-33952723	K562	blood:	n/a
23	chr2:33948457-33948507	SK-N-SH_RA	brain:	n/a
24	chr2:33954347-33954397	Caco-2	colon:	n/a
25	chr2:33951647-33951697	HAEpiC	amniotic membrane:	n/a
26	chr2:33951647-33951697	HUVEC	blood vessel:	n/a
27	chr2:33954735-33954785	NH-A	brain:	n/a
28	chr2:33953203-33953253	AoSMC	blood vessel:	n/a
29	chr2:33952509-33952559	U87	brain:	n/a
30	chr2:33953437-33953487	GM12878	blood:	n/a
31	chr2:33953195-33953245	Jurkat	blood:	n/a
32	chr2:33954043-33954093	GM12891	blood:	n/a
33	chr2:33952423-33952473	HL-60	blood:	n/a
34	chr2:33948457-33948507	IMR90	lung:	fetal
35	chr2:33952509-33952559	HEK293	kidney:	embryo
36	chr2:33953370-33953420	HRPEpiC	eye:	n/a
37	chr2:33954043-33954093	U87	brain:	n/a
38	chr2:33954043-33954093	HCM	heart:	n/a
39	chr2:33953203-33953253	Caco-2	colon:	n/a
40	chr2:33952423-33952473	HEK293	kidney:	embryo
41	chr2:33952423-33952473	HepG2	liver:	n/a
42	chr2:33953437-33953487	HL-60	blood:	n/a
43	chr2:33953195-33953245	GM12891	blood:	n/a
44	chr2:33954347-33954397	HCT-116	colon:	n/a
45	chr2:33952423-33952473	HMEC	breast:	n/a
46	chr2:33953437-33953487	SK-N-SH	brain:	n/a
47	chr2:33954735-33954785	AG04449	skin:	fetal
48	chr2:33954735-33954785	AG04450	lung:	fetal
49	chr2:33954347-33954397	HRPEpiC	eye:	n/a
50	chr2:33953370-33953420	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:34008516..34010441-chr2:34014849..34016681,2	MCF-7	breast:
2	chr2:33973736..33977470-chr2:33981372..33984191,3	K562	blood:
3	chr2:33938363..33940880-chr2:33942730..33944320,2	K562	blood:
4	chr2:33973736..33977470-chr2:33981372..33984191,3	K562	blood:
5	chr2:34008516..34010441-chr2:34014849..34016681,2	MCF-7	breast:
6	chr2:33994888..33996887-chr2:34002074..34004966,2	MCF-7	breast:
7	chr2:34033415..34035422-chr2:34038221..34040306,2	MCF-7	breast:
8	chr2:34056369..34058032-chr2:34058034..34060009,2	K562	blood:
9	chr2:34056369..34058032-chr2:34058034..34060009,2	K562	blood:
10	chr2:34033415..34035422-chr2:34038221..34040306,2	MCF-7	breast:
11	chr2:33938363..33940880-chr2:33942730..33944320,2	K562	blood:
12	chr11:62608939..62609489-chr2:34040620..34041120,2	Hela-S3	cervix:
13	chr2:33994888..33996887-chr2:34002074..34004966,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM98A-4	chr2:33947328-33947937	NONHSAT147081
2	lnc-RASGRP3-1	chr2:34080755-34080820	ENSG00000203386
3	lnc-FAM98A-4	chr2:33948350-33948577	NONHSAT147081
4	lnc-RASGRP3-1	chr2:34080755-34080820	ENSG00000203386

Variant related genes	Relation type
SLC25A5P2	TF binding region
MYADML	TF binding region
ENSG00000264267	TF binding region
SLC25A5P2	CpG island
MYADML	CpG island
ENSG00000264267	CpG island
ENSG00000133316	chromatin interactions

Extended variants
information (count: 5115 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5115 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6543739	chr2:33936701-33936702	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188541053	chr2:33936706-33936707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192271643	chr2:33936786-33936787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115958167	chr2:33936796-33936797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529294859	chr2:33936814-33936815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147400878	chr2:33936862-33936863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139629324	chr2:33936900-33936901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77942124	chr2:33936906-33936907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74262208	chr2:33936926-33936927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184206694	chr2:33936984-33936985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189399478	chr2:33936991-33936992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550081778	chr2:33937032-33937033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563599830	chr2:33937042-33937043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566339622	chr2:33937111-33937112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181959287	chr2:33937117-33937118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555461573	chr2:33937124-33937125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74605717	chr2:33937141-33937142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115492843	chr2:33937154-33937155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533989165	chr2:33937159-33937160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556781311	chr2:33937170-33937171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556332036	chr2:33937175-33937176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187293336	chr2:33937253-33937254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567307855	chr2:33937280-33937281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536275129	chr2:33937282-33937283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556160616	chr2:33937308-33937309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548712138	chr2:33937318-33937319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145309099	chr2:33937319-33937320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147629384	chr2:33937343-33937344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558839410	chr2:33937366-33937367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572647954	chr2:33937389-33937390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78765162	chr2:33937390-33937391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554681384	chr2:33937395-33937396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574461137	chr2:33937474-33937475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140452024	chr2:33937481-33937482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563288495	chr2:33937505-33937506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532407583	chr2:33937509-33937510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546081409	chr2:33937605-33937606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149981546	chr2:33937641-33937642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578145857	chr2:33937697-33937698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547552396	chr2:33937712-33937713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567394492	chr2:33937725-33937726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530149784	chr2:33937753-33937754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375549111	chr2:33937769-33937770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116654267	chr2:33937786-33937787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569720183	chr2:33937794-33937795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538963313	chr2:33937797-33937798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs61696126	chr2:33937798-33937799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397984270	chr2:33937804-33937805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112082301	chr2:33937812-33937813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559244169	chr2:33937820-33937821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33930000-33937400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:33930200-33937000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:33930200-33937000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr2:33930400-33937000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr2:33935000-33937600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:33936400-33938000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:33936600-33938400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr2:33937000-33937600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr2:33937000-33937800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:33937000-33938200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr2:33937000-33938400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr2:33937200-33937600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr2:33937200-33938400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:33937400-33937600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr2:33937400-33938200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr2:33938000-33938400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:33938400-33941800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:33938600-33942200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:33943800-33945200	Enhancers	HUVEC	blood vessel
20	chr2:33951400-33951600	Enhancers	K562	blood
21	chr2:33952200-33952400	Enhancers	K562	blood
22	chr2:33952200-33953200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:33952200-33953200	ZNF genes & repeats	Spleen	Spleen
24	chr2:33954800-33955200	Enhancers	GM12878-XiMat	blood
25	chr2:33955000-33955800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr2:33955200-33955600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr2:33955200-33955800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr2:33955400-33955800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr2:33955400-33955800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr2:33955800-33960200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr2:33960200-33960600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:33984200-33984400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:33986800-33987000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr2:33986800-33987000	Active TSS	Gastric	stomach
35	chr2:33986800-33987200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr2:33987000-33987200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr2:33987000-34000200	Weak transcription	Gastric	stomach
38	chr2:33987200-33987600	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr2:33987200-33988400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr2:33988000-33988800	Enhancers	Placenta Amnion	Placenta Amnion
41	chr2:33988000-33992200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:33988200-33988400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:33988200-33988800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:33988200-33989200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:33988200-33991200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:33988400-33989000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:33988400-33989000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr2:33988400-33989000	Enhancers	Lung	lung
49	chr2:33988400-33989800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:33988400-33991000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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