Variant report

Variant	esv1006063
Chromosome Location	chr19:40368832-40385337
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:375)
CpG islands
(count:490)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40372209-40372386	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40377903-40377918	HepG2	liver:	n/a	n/a
3	ATF1	chr19:40372283-40372483	K562	blood:	n/a	n/a
4	ATF2	chr19:40372199-40372449	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:40372203-40372491	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr19:40372229-40372663	GM12878	blood:	n/a	chr19:40372417-40372430
7	BHLHE40	chr19:40372341-40372378	HepG2	liver:	n/a	n/a
8	BHLHE40	chr19:40378004-40378342	HepG2	liver:	n/a	n/a
9	BHLHE40	chr19:40372174-40372382	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:40372310-40372375	K562	blood:	n/a	n/a
11	CBX3	chr19:40372094-40372533	K562	blood:	n/a	n/a
12	CEBPB	chr19:40369307-40369516	HepG2	liver:	n/a	n/a
13	CTCF	chr19:40372260-40372410	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr19:40372260-40372410	HAc	cerebellar:	n/a	n/a
15	CTCF	chr19:40372217-40372482	H1-hESC	embryonic stem cell:	n/a	chr19:40372450-40372463
16	CTCF	chr19:40372240-40372390	AG10803	skin:	n/a	n/a
17	CTCF	chr19:40372210-40372457	A549	lung:	n/a	n/a
18	CTCF	chr19:40372238-40372426	GM20000	blood:	n/a	n/a
19	CTCF	chr19:40372260-40372410	HEK293	kidney:	n/a	n/a
20	CTCF	chr19:40370900-40371050	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr19:40372260-40372410	HRE	kidney:	n/a	n/a
22	CTCF	chr19:40372280-40372430	MCF-7	breast:	n/a	n/a
23	CTCF	chr19:40372262-40372466	MCF-7	breast:	n/a	chr19:40372450-40372463
24	CTCF	chr19:40372240-40372390	AG09309	skin:	n/a	n/a
25	CTCF	chr19:40372600-40372750	HEK293	kidney:	n/a	n/a
26	CTCF	chr19:40372083-40372671	A549	lung:	n/a	chr19:40372450-40372463
27	CTCF	chr19:40372260-40372410	HMEC	breast:	n/a	n/a
28	CTCF	chr19:40372280-40372430	NHLF	lung:	n/a	n/a
29	CTCF	chr19:40372220-40372541	Kidney_OC	kidney:	n/a	chr19:40372450-40372463
30	CTCF	chr19:40372151-40372680	A549	lung:	n/a	chr19:40372450-40372463
31	CTCF	chr19:40372203-40372462	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr19:40372280-40372430	AG04450	lung:	n/a	n/a
33	CTCF	chr19:40372280-40372430	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr19:40372280-40372430	HMF	breast:	n/a	n/a
35	CTCF	chr19:40372224-40372474	GM13976	blood:	n/a	chr19:40372450-40372463
36	CTCF	chr19:40372235-40372450	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr19:40372280-40372430	GM12869	blood:	n/a	n/a
38	CTCF	chr19:40382398-40382766	K562	blood:	n/a	n/a
39	CTCF	chr19:40372260-40372410	WI-38	lung:	n/a	n/a
40	CTCF	chr19:40372210-40372497	GM13977	blood:	n/a	chr19:40372450-40372463
41	CTCF	chr19:40372210-40372452	MCF-7	breast:	n/a	n/a
42	CTCF	chr19:40372260-40372410	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr19:40372207-40372478	Hela-S3	cervix:	n/a	chr19:40372450-40372463
44	CTCF	chr19:40372280-40372430	HCT-116	colon:	n/a	n/a
45	CTCF	chr19:40372123-40372643	K562	blood:	n/a	chr19:40372450-40372463
46	CTCF	chr19:40372260-40372410	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr19:40372137-40372441	HepG2	liver:	n/a	n/a
48	CTCF	chr19:40372205-40372488	NHEK	skin:	n/a	chr19:40372450-40372463
49	CTCF	chr19:40372041-40372503	A549	lung:	n/a	chr19:40372450-40372463
50	CTCF	chr19:40372243-40372561	GM10248	blood:	n/a	chr19:40372450-40372463

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40375973-40376023	HCPEpiC	choroid plexus:	n/a
2	chr19:40379680-40379730	HepG2	liver:	n/a
3	chr19:40375973-40376023	HCPEpiC	choroid plexus:	n/a
4	chr19:40379680-40379730	HepG2	liver:	n/a
5	chr19:40379680-40379730	AG10803	skin:	n/a
6	chr19:40376883-40376933	HCF	heart:	n/a
7	chr19:40375973-40376023	T-47D	breast:	n/a
8	chr19:40372977-40373027	ProgFib	skin:	n/a
9	chr19:40375973-40376023	NB4	blood:	n/a
10	chr19:40380853-40380903	RPTEC	kidney:	n/a
11	chr19:40376883-40376933	GM12891	blood:	n/a
12	chr19:40379680-40379730	NT2-D1	testis:	n/a
13	chr19:40372977-40373027	NB4	blood:	n/a
14	chr19:40368830-40368880	SK-N-SH	brain:	n/a
15	chr19:40375973-40376023	AG10803	skin:	n/a
16	chr19:40368830-40368880	HCPEpiC	choroid plexus:	n/a
17	chr19:40380319-40380369	ovcar-3	ovarian:	n/a
18	chr19:40372977-40373027	RPTEC	kidney:	n/a
19	chr19:40375973-40376023	PrEC	prostate:	n/a
20	chr19:40376883-40376933	ProgFib	skin:	n/a
21	chr19:40380853-40380903	BJ	skin:	n/a
22	chr19:40380853-40380903	HepG2	liver:	n/a
23	chr19:40368830-40368880	Hepatocyte	liver:	n/a
24	chr19:40368830-40368880	GM12878	blood:	n/a
25	chr19:40368830-40368880	HEK293	kidney:	embryo
26	chr19:40380853-40380903	T-47D	breast:	n/a
27	chr19:40368830-40368880	NHDF-neo	bronchial:	n/a
28	chr19:40375973-40376023	BJ	skin:	n/a
29	chr19:40379680-40379730	SAEC	small airway:	n/a
30	chr19:40375973-40376023	Hepatocyte	liver:	n/a
31	chr19:40380319-40380369	H1-hESC	embryonic stem cell:	embryo
32	chr19:40377434-40377484	GM06990	blood:	n/a
33	chr19:40380853-40380903	K562	blood:	n/a
34	chr19:40368830-40368880	HMEC	breast:	n/a
35	chr19:40376883-40376933	H1-hESC	embryonic stem cell:	embryo
36	chr19:40380319-40380369	SAEC	small airway:	n/a
37	chr19:40375973-40376023	HEEpiC	esophagus:	n/a
38	chr19:40379680-40379730	GM06990	blood:	n/a
39	chr19:40380319-40380369	Hepatocyte	liver:	n/a
40	chr19:40380319-40380369	U87	brain:	n/a
41	chr19:40377434-40377484	AG09309	skin:	n/a
42	chr19:40379680-40379730	HRCEpiC	kidney:	n/a
43	chr19:40368830-40368880	HNPCEpiC	eye:	n/a
44	chr19:40372977-40373027	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:40376883-40376933	GM12878	blood:	n/a
46	chr19:40377434-40377484	AG04449	skin:	fetal
47	chr19:40368830-40368880	Jurkat	blood:	n/a
48	chr19:40380853-40380903	HCM	heart:	n/a
49	chr19:40380319-40380369	K562	blood:	n/a
50	chr19:40377434-40377484	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:40371880..40372846-chr19:40476486..40477439,2	MCF-7	breast:
2	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:

No data

Variant related genes	Relation type
FCGBP	TF binding region
FCGBP	CpG island
ENSG00000013275	chromatin interactions

Extended variants
information (count: 576 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148053727	chr19:40368835-40368836	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371488968	chr19:40368837-40368838	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370209965	chr19:40368838-40368839	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539178516	chr19:40368841-40368842	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145138197	chr19:40368870-40368871	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375898948	chr19:40368871-40368872	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150967580	chr19:40368903-40368904	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554305659	chr19:40368907-40368908	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377718213	chr19:40368908-40368909	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371381755	chr19:40368912-40368913	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374280646	chr19:40368920-40368921	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566291851	chr19:40368954-40368955	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536430206	chr19:40368962-40368963	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555111454	chr19:40368968-40368969	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576665743	chr19:40368997-40368998	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543666649	chr19:40369071-40369072	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180931312	chr19:40369096-40369097	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372024790	chr19:40369125-40369126	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372448814	chr19:40369126-40369127	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576424947	chr19:40369150-40369151	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540754235	chr19:40369155-40369156	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12981005	chr19:40369163-40369164	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559165789	chr19:40369166-40369167	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370689239	chr19:40369196-40369197	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541682961	chr19:40369203-40369204	Weak transcription Bivalent Enhancer Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs373984500	chr19:40369213-40369214	Weak transcription Bivalent Enhancer Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs563453680	chr19:40369271-40369272	Weak transcription Bivalent Enhancer Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530726365	chr19:40369306-40369307	Weak transcription Bivalent Enhancer Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs552492354	chr19:40369328-40369329	Weak transcription Bivalent Enhancer Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs571717397	chr19:40369399-40369400	Weak transcription Bivalent Enhancer Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs200105955	chr19:40369411-40369412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200502502	chr19:40369429-40369430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61233386	chr19:40369430-40369431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7258336	chr19:40369431-40369432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75963372	chr19:40369432-40369433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs56403941	chr19:40369435-40369436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77786713	chr19:40369449-40369450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566057226	chr19:40369461-40369462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6508921	chr19:40369462-40369463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548506896	chr19:40369560-40369561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs67861877	chr19:40369566-40369567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570219964	chr19:40369588-40369589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537394930	chr19:40369603-40369604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10422500	chr19:40369619-40369620	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs113245187	chr19:40369624-40369625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368334762	chr19:40369629-40369630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534329327	chr19:40369633-40369634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552902162	chr19:40369634-40369635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs58339973	chr19:40369649-40369650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7257897	chr19:40369681-40369682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40349800-40369000	Weak transcription	Brain Anterior Caudate	brain
2	chr19:40350400-40372200	Weak transcription	Dnd41	blood
3	chr19:40352000-40372600	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr19:40352400-40372400	Weak transcription	Fetal Intestine Large	intestine
5	chr19:40354200-40370800	Weak transcription	Fetal Brain Female	brain
6	chr19:40354600-40372200	Weak transcription	HepG2	liver
7	chr19:40355200-40372200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr19:40358400-40372200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr19:40359800-40369600	Weak transcription	Fetal Muscle Leg	muscle
10	chr19:40361000-40372200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr19:40361200-40374000	Weak transcription	Pancreas	Pancrea
12	chr19:40364400-40372200	Weak transcription	Right Atrium	heart
13	chr19:40364400-40372400	Weak transcription	Gastric	stomach
14	chr19:40364600-40369200	Weak transcription	Colonic Mucosa	Colon
15	chr19:40365800-40372200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr19:40365800-40372600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr19:40366000-40369000	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr19:40366200-40372800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr19:40366600-40372400	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr19:40367000-40369000	Weak transcription	Stomach Mucosa	stomach
21	chr19:40367000-40372400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr19:40367000-40373400	Weak transcription	Fetal Stomach	stomach
23	chr19:40368000-40371400	Strong transcription	Fetal Intestine Small	intestine
24	chr19:40368400-40369000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr19:40368600-40371200	Strong transcription	Primary T cells from cord blood	blood
26	chr19:40368800-40369800	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr19:40368800-40371200	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr19:40369000-40369200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr19:40369000-40369400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
30	chr19:40369000-40369800	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr19:40369000-40370000	Strong transcription	Stomach Mucosa	stomach
32	chr19:40369200-40369400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr19:40369200-40369400	Active TSS	Brain Anterior Caudate	brain
34	chr19:40369200-40369800	Strong transcription	Colonic Mucosa	Colon
35	chr19:40369800-40375800	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr19:40369800-40402600	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr19:40369800-40404000	Weak transcription	Colonic Mucosa	Colon
38	chr19:40370000-40371600	Weak transcription	Stomach Mucosa	stomach
39	chr19:40371200-40402800	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr19:40371200-40404000	Weak transcription	Primary T cells from cord blood	blood
41	chr19:40371400-40391000	Weak transcription	Fetal Intestine Small	intestine
42	chr19:40372200-40372400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr19:40372200-40372400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr19:40372200-40372400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr19:40372200-40372400	ZNF genes & repeats	Right Atrium	heart
46	chr19:40372200-40372600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr19:40372200-40372600	Enhancers	Primary B cells from peripheral blood	blood
48	chr19:40372200-40372600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr19:40372200-40372600	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr19:40372200-40372600	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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