Variant report

Variant	nsv579512
Chromosome Location	chr19:40368522-40385744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:376)
CpG islands
(count:488)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:376 , 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	chr19:40377903-40377918	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40372209-40372386	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	chr19:40378004-40378342	HepG2	liver:	n/a	n/a
8	BHLHE40	chr19:40372341-40372378	HepG2	liver:	n/a	n/a
9	BHLHE40	chr19:40372310-40372375	K562	blood:	n/a	n/a
10	BHLHE40	chr19:40372174-40372382	GM12878	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	chr19:40372240-40372390	NHDF-neo	bronchial:	n/a	n/a
14	CTCF	chr19:40372240-40372390	SAEC	small airway:	n/a	n/a
15	CTCF	chr19:40372122-40372678	K562	blood:	n/a	chr19:40372450-40372463
16	CTCF	chr19:40372243-40372561	GM10248	blood:	n/a	chr19:40372450-40372463
17	CTCF	chr19:40372123-40372643	K562	blood:	n/a	chr19:40372450-40372463
18	CTCF	chr19:40372203-40372462	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr19:40372260-40372410	K562	blood:	n/a	n/a
20	CTCF	chr19:40372240-40372390	GM12801	blood:	n/a	n/a
21	CTCF	chr19:40372280-40372430	GM12875	blood:	n/a	n/a
22	CTCF	chr19:40372220-40372445	MCF-7	breast:	n/a	n/a
23	CTCF	chr19:40377762-40377797	LNCaP	prostate:	n/a	n/a
24	CTCF	chr19:40372260-40372410	AG04449	skin:	n/a	n/a
25	CTCF	chr19:40372280-40372430	GM12866	blood:	n/a	n/a
26	CTCF	chr19:40372280-40372430	NHEK	skin:	n/a	n/a
27	CTCF	chr19:40372178-40372518	GM10266	blood:	n/a	chr19:40372450-40372463
28	CTCF	chr19:40372241-40372447	ProgFib	skin:	n/a	n/a
29	CTCF	chr19:40372248-40372468	Lung_OC	lung:	n/a	chr19:40372450-40372463
30	CTCF	chr19:40372253-40372401	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr19:40372237-40372435	HepG2	liver:	n/a	n/a
32	CTCF	chr19:40372280-40372430	SAEC	small airway:	n/a	n/a
33	CTCF	chr19:40372135-40372547	K562	blood:	n/a	chr19:40372450-40372463
34	CTCF	chr19:40372260-40372410	HL-60	blood:	n/a	n/a
35	CTCF	chr19:40372280-40372430	HVMF	connective:	n/a	n/a
36	CTCF	chr19:40372110-40372651	SK-N-SH	brain:	n/a	chr19:40372450-40372463
37	CTCF	chr19:40372260-40372410	BJ	skin:	n/a	n/a
38	CTCF	chr19:40372207-40372473	GM12891	blood:	n/a	chr19:40372450-40372463
39	CTCF	chr19:40372260-40372410	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr19:40372280-40372430	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr19:40372217-40372482	H1-hESC	embryonic stem cell:	n/a	chr19:40372450-40372463
42	CTCF	chr19:40372260-40372410	HEK293	kidney:	n/a	n/a
43	CTCF	chr19:40372280-40372430	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr19:40372260-40372410	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr19:40372280-40372430	RPTEC	kidney:	n/a	n/a
46	CTCF	chr19:40382647-40382771	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr19:40372207-40372478	Hela-S3	cervix:	n/a	chr19:40372450-40372463
48	CTCF	chr19:40372280-40372430	HepG2	liver:	n/a	n/a
49	CTCF	chr19:40372236-40372442	ECC-1	luminal epithelium:	n/a	n/a
50	CTCF	chr19:40372236-40372444	MCF-7	breast:	n/a	n/a

(count:488 , 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	HEK293	kidney:	embryo
2	chr19:40375973-40376023	GM06990	blood:	n/a
3	chr19:40375973-40376023	GM12891	blood:	n/a
4	chr19:40372977-40373027	K562	blood:	n/a
5	chr19:40368830-40368880	BJ	skin:	n/a
6	chr19:40379680-40379730	HEEpiC	esophagus:	n/a
7	chr19:40379680-40379730	PFSK-1	brain:	n/a
8	chr19:40376883-40376933	AG09319	gingival:	n/a
9	chr19:40372977-40373027	PANC-1	pancreas:	n/a
10	chr19:40380853-40380903	T-47D	breast:	n/a
11	chr19:40368830-40368880	NHBE	bronchial:	n/a
12	chr19:40377434-40377484	HEK293	kidney:	embryo
13	chr19:40377434-40377484	H1-hESC	embryonic stem cell:	embryo
14	chr19:40372977-40373027	NT2-D1	testis:	n/a
15	chr19:40380853-40380903	BJ	skin:	n/a
16	chr19:40375973-40376023	HL-60	blood:	n/a
17	chr19:40377434-40377484	AG09309	skin:	n/a
18	chr19:40377434-40377484	HCF	heart:	n/a
19	chr19:40372977-40373027	SK-N-SH_RA	brain:	n/a
20	chr19:40377434-40377484	ProgFib	skin:	n/a
21	chr19:40375973-40376023	BE2_C	brain:	n/a
22	chr19:40377434-40377484	HIPEpiC	eye:	n/a
23	chr19:40368830-40368880	H1-hESC	embryonic stem cell:	embryo
24	chr19:40375973-40376023	ProgFib	skin:	n/a
25	chr19:40375973-40376023	SAEC	small airway:	n/a
26	chr19:40372977-40373027	AG04450	lung:	fetal
27	chr19:40368830-40368880	HCM	heart:	n/a
28	chr19:40368830-40368880	AG10803	skin:	n/a
29	chr19:40379680-40379730	H1-hESC	embryonic stem cell:	embryo
30	chr19:40368830-40368880	HRPEpiC	eye:	n/a
31	chr19:40375973-40376023	HRE	kidney:	n/a
32	chr19:40380319-40380369	HRPEpiC	eye:	n/a
33	chr19:40380853-40380903	HMEC	breast:	n/a
34	chr19:40368830-40368880	RPTEC	kidney:	n/a
35	chr19:40377434-40377484	ECC-1	luminal epithelium:	n/a
36	chr19:40368830-40368880	SK-N-SH	brain:	n/a
37	chr19:40377434-40377484	IMR90	lung:	fetal
38	chr19:40368830-40368880	Hela-S3	cervix:	n/a
39	chr19:40375973-40376023	Hela-S3	cervix:	n/a
40	chr19:40372977-40373027	CMK	blood:	n/a
41	chr19:40380319-40380369	BJ	skin:	n/a
42	chr19:40380853-40380903	Caco-2	colon:	n/a
43	chr19:40380853-40380903	Hepatocyte	liver:	n/a
44	chr19:40377434-40377484	NH-A	brain:	n/a
45	chr19:40375973-40376023	AoSMC	blood vessel:	n/a
46	chr19:40372977-40373027	GM12878	blood:	n/a
47	chr19:40379680-40379730	AoSMC	blood vessel:	n/a
48	chr19:40379680-40379730	Hepatocyte	liver:	n/a
49	chr19:40380853-40380903	ovcar-3	ovarian:	n/a
50	chr19:40380853-40380903	HepG2	liver:	n/a

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

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

No data

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

Extended variants
information (count: 617 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554417983	chr19:40368525-40368526	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572540106	chr19:40368526-40368527	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374411567	chr19:40368538-40368539	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543353045	chr19:40368539-40368540	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554943335	chr19:40368553-40368554	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576023060	chr19:40368554-40368555	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140562758	chr19:40368577-40368578	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372333418	chr19:40368602-40368603	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201926065	chr19:40368605-40368606	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150027077	chr19:40368619-40368620	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543072093	chr19:40368629-40368630	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564493439	chr19:40368676-40368677	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532085056	chr19:40368678-40368679	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144966876	chr19:40368683-40368684	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199714018	chr19:40368684-40368685	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368994804	chr19:40368697-40368698	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144631134	chr19:40368707-40368708	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372533131	chr19:40368737-40368738	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377237982	chr19:40368749-40368750	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529826298	chr19:40368750-40368751	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138525431	chr19:40368764-40368765	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569864250	chr19:40368779-40368780	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530808402	chr19:40368802-40368803	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140207614	chr19:40368805-40368806	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368547780	chr19:40368806-40368807	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200976557	chr19:40368819-40368820	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143612696	chr19:40368829-40368830	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571629241	chr19:40368831-40368832	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148053727	chr19:40368835-40368836	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371488968	chr19:40368837-40368838	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370209965	chr19:40368838-40368839	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539178516	chr19:40368841-40368842	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145138197	chr19:40368870-40368871	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375898948	chr19:40368871-40368872	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150967580	chr19:40368903-40368904	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554305659	chr19:40368907-40368908	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377718213	chr19:40368908-40368909	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371381755	chr19:40368912-40368913	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374280646	chr19:40368920-40368921	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566291851	chr19:40368954-40368955	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536430206	chr19:40368962-40368963	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555111454	chr19:40368968-40368969	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576665743	chr19:40368997-40368998	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543666649	chr19:40369071-40369072	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180931312	chr19:40369096-40369097	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372024790	chr19:40369125-40369126	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372448814	chr19:40369126-40369127	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576424947	chr19:40369150-40369151	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540754235	chr19:40369155-40369156	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12981005	chr19:40369163-40369164	Weak transcription Enhancers Bivalent Enhancer 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:75 , 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	chr19:40367000-40368800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr19:40367000-40369000	Weak transcription	Stomach Mucosa	stomach
22	chr19:40367000-40372400	Weak transcription	Fetal Muscle Trunk	muscle
23	chr19:40367000-40373400	Weak transcription	Fetal Stomach	stomach
24	chr19:40367200-40368600	Weak transcription	Primary T cells from cord blood	blood
25	chr19:40367200-40368800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr19:40368000-40371400	Strong transcription	Fetal Intestine Small	intestine
27	chr19:40368400-40369000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr19:40368600-40371200	Strong transcription	Primary T cells from cord blood	blood
29	chr19:40368800-40369800	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr19:40368800-40371200	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr19:40369000-40369200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr19:40369000-40369400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
33	chr19:40369000-40369800	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr19:40369000-40370000	Strong transcription	Stomach Mucosa	stomach
35	chr19:40369200-40369400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr19:40369200-40369400	Active TSS	Brain Anterior Caudate	brain
37	chr19:40369200-40369800	Strong transcription	Colonic Mucosa	Colon
38	chr19:40369800-40375800	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr19:40369800-40402600	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr19:40369800-40404000	Weak transcription	Colonic Mucosa	Colon
41	chr19:40370000-40371600	Weak transcription	Stomach Mucosa	stomach
42	chr19:40371200-40402800	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr19:40371200-40404000	Weak transcription	Primary T cells from cord blood	blood
44	chr19:40371400-40391000	Weak transcription	Fetal Intestine Small	intestine
45	chr19:40372200-40372400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr19:40372200-40372400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr19:40372200-40372400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr19:40372200-40372400	ZNF genes & repeats	Right Atrium	heart
49	chr19:40372200-40372600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr19:40372200-40372600	Enhancers	Primary B cells from peripheral blood	blood

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