Variant report

Variant	rs2537697
Chromosome Location	chr19:42807321-42807322
allele	A/G
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	SP1	chr19:42805624-42807490	A549	lung:	n/a	chr19:42806832-42806844 chr19:42806762-42806776 chr19:42806533-42806543 chr19:42806961-42806970 chr19:42806798-42806807 chr19:42806864-42806875 chr19:42806240-42806252 chr19:42806832-42806843 chr19:42806832-42806844 chr19:42806240-42806252 chr19:42806076-42806090 chr19:42806235-42806247 chr19:42806864-42806876 chr19:42806984-42806998 chr19:42806833-42806842 chr19:42806235-42806247 chr19:42806834-42806843 chr19:42806241-42806250 chr19:42806533-42806543 chr19:42806236-42806245 chr19:42806804-42806815 chr19:42806987-42806999 chr19:42806988-42806997 chr19:42806865-42806874 chr19:42806801-42806815
2	USF1	chr19:42806290-42807579	A549	lung:	n/a	n/a
3	RELA	chr19:42806564-42807425	GM12891	blood:	n/a	n/a
4	TCF12	chr19:42806220-42807365	ECC-1	luminal epithelium:	n/a	n/a
5	IRF1	chr19:42806497-42807567	K562	blood:	n/a	chr19:42806864-42806878 chr19:42807409-42807423 chr19:42807413-42807427 chr19:42807413-42807423 chr19:42806530-42806544
6	E2F6	chr19:42806009-42807336	H1-hESC	embryonic stem cell:	n/a	chr19:42806715-42806726 chr19:42806341-42806350 chr19:42806865-42806877
7	MAFF	chr19:42806540-42807647	K562	blood:	n/a	n/a
8	GATA3	chr19:42805611-42807702	A549	lung:	n/a	chr19:42805851-42805859 chr19:42805910-42805917
9	TCF12	chr19:42805649-42807906	A549	lung:	n/a	n/a
10	POLR2A	chr19:42805997-42807650	PFSK-1	brain:	n/a	n/a
11	IRF1	chr19:42806431-42807321	K562	blood:	n/a	chr19:42806864-42806878 chr19:42806530-42806544
12	MYC	chr19:42806031-42807403	K562	blood:	n/a	chr19:42807332-42807341 chr19:42806957-42806967
13	CREB1	chr19:42806127-42807340	HepG2	liver:	n/a	n/a
14	MXI1	chr19:42805818-42807634	IMR90	lung:	n/a	n/a
15	CHD1	chr19:42805975-42807449	IMR90	lung:	n/a	chr19:42806987-42806997
16	REST	chr19:42805542-42807717	H1-neurons	neurons:	n/a	chr19:42806242-42806255 chr19:42806850-42806868 chr19:42806021-42806041
17	HCFC1	chr19:42806517-42807335	K562	blood:	n/a	n/a
18	REST	chr19:42806043-42807466	A549	lung:	n/a	chr19:42806242-42806255 chr19:42806850-42806868
19	MYC	chr19:42805959-42807401	K562	blood:	n/a	chr19:42807332-42807341 chr19:42806957-42806967
20	EP300	chr19:42806539-42807455	K562	blood:	n/a	chr19:42807418-42807432
21	RFX5	chr19:42807172-42807337	K562	blood:	n/a	n/a
22	MAX	chr19:42805967-42807483	ECC-1	luminal epithelium:	n/a	chr19:42807332-42807341 chr19:42806957-42806967
23	POLR2A	chr19:42805951-42807626	K562	blood:	n/a	n/a
24	MAX	chr19:42805981-42807389	HepG2	liver:	n/a	chr19:42807332-42807341 chr19:42806957-42806967
25	MAX	chr19:42805951-42807326	MCF-7	breast:	n/a	chr19:42806957-42806967
26	CEBPB	chr19:42807113-42807406	K562	blood:	n/a	n/a
27	RELA	chr19:42806577-42807353	GM18951	blood:	n/a	n/a
28	TBL1XR1	chr19:42806408-42807437	GM12878	blood:	n/a	n/a
29	SREBP1	chr19:42806146-42807688	GM12878	blood:	n/a	n/a
30	EGR1	chr19:42806262-42807373	K562	blood:	n/a	chr19:42806954-42806967 chr19:42806860-42806873 chr19:42806536-42806547 chr19:42806768-42806782 chr19:42806860-42806873 chr19:42806534-42806549 chr19:42806615-42806625 chr19:42806959-42806969 chr19:42806859-42806874
31	EP300	chr19:42806368-42807327	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAX	chr19:42805899-42807504	HCT-116	colon:	n/a	chr19:42807332-42807341 chr19:42806957-42806967
33	EP300	chr19:42806497-42807326	GM12878	blood:	n/a	n/a
34	ZMIZ1	chr19:42806537-42807400	K562	blood:	n/a	n/a
35	MAZ	chr19:42805812-42807329	IMR90	lung:	n/a	chr19:42806957-42806967
36	MAX	chr19:42806321-42807409	GM12878	blood:	n/a	chr19:42807332-42807341 chr19:42806957-42806967
37	MTA3	chr19:42805851-42807615	GM12878	blood:	n/a	n/a
38	MAX	chr19:42806050-42807333	H1-hESC	embryonic stem cell:	n/a	chr19:42806957-42806967
39	TCF12	chr19:42806317-42807438	A549	lung:	n/a	n/a
40	GATA2	chr19:42807054-42807622	SH-SY5Y	brain:	n/a	n/a
41	POLR2A	chr19:42805149-42807770	PFSK-1	brain:	n/a	n/a
42	JUND	chr19:42805980-42807400	K562	blood:	n/a	chr19:42806960-42806969 chr19:42806957-42806966 chr19:42806238-42806247 chr19:42806959-42806968
43	GATA3	chr19:42806398-42807389	SK-N-SH	brain:	n/a	n/a
44	MAX	chr19:42805901-42807374	K562	blood:	n/a	chr19:42807332-42807341 chr19:42806957-42806967
45	RUNX3	chr19:42806379-42807385	GM12878	blood:	n/a	n/a
46	ETS1	chr19:42806219-42807484	A549	lung:	n/a	chr19:42806958-42806969 chr19:42806957-42806968 chr19:42806335-42806346 chr19:42806960-42806971
47	EP300	chr19:42806252-42807541	A549	lung:	n/a	chr19:42807418-42807432 chr19:42806294-42806307
48	JUND	chr19:42805981-42807404	A549	lung:	n/a	chr19:42806960-42806969 chr19:42806957-42806966 chr19:42806238-42806247 chr19:42806959-42806968
49	POLR2A	chr19:42806097-42807461	K562	blood:	n/a	n/a
50	BCL3	chr19:42806352-42807460	A549	lung:	n/a	chr19:42807190-42807199

No.	Distal block	Cell Line	Cell type
1	chr19:42806642..42809220-chr19:42829976..42831705,2	K562	blood:
2	chr19:42720843..42724936-chr19:42805318..42808035,4	MCF-7	breast:
3	chr19:42579835..42581809-chr19:42805426..42808329,2	K562	blood:
4	chr19:42805304..42808319-chr19:42899510..42903078,3	K562	blood:
5	chr19:42745670..42748955-chr19:42805967..42808847,6	K562	blood:
6	chr19:42771398..42774307-chr19:42804493..42807877,4	MCF-7	breast:
7	chr19:42746221..42749028-chr19:42806673..42809269,4	K562	blood:
8	chr19:42804082..42810862-chr19:42813351..42818872,10	K562	blood:
9	chr19:42757990..42761273-chr19:42805380..42807935,4	MCF-7	breast:
10	chr19:42756858..42760226-chr19:42804706..42807905,7	K562	blood:
11	chr19:42754219..42757685-chr19:42805206..42807524,5	MCF-7	breast:
12	chr19:42806459..42808702-chr19:42827247..42830028,2	K562	blood:
13	chr19:42756858..42762075-chr19:42803237..42807691,9	K562	blood:
14	chr19:42786948..42794333-chr19:42803465..42809501,23	K562	blood:
15	chr19:42787763..42791073-chr19:42804241..42808628,6	MCF-7	breast:
16	chr19:42804822..42808346-chr19:42815036..42819132,8	MCF-7	breast:
17	chr19:42757687..42760394-chr19:42806453..42809186,2	MCF-7	breast:
18	chr19:42745110..42750037-chr19:42804255..42809210,7	MCF-7	breast:
19	chr19:42804664..42808164-chr19:42828676..42831528,3	MCF-7	breast:
20	chr19:42722916..42725353-chr19:42805921..42808141,2	K562	blood:
21	chr19:42783298..42787362-chr19:42802681..42808039,8	MCF-7	breast:
22	chr19:42387685..42389812-chr19:42806888..42808559,2	K562	blood:
23	chr19:42804981..42810862-chr19:42813585..42819261,9	K562	blood:
24	chr19:42771105..42773106-chr19:42805155..42808634,5	K562	blood:

Variant related genes	Relation type
PAFAH1B3	TF binding region
PRR19	TF binding region
ENSG00000204957	Chromatin interaction
ENSG00000160570	Chromatin interaction
ENSG00000105722	Chromatin interaction
ENSG00000268643	Chromatin interaction
ENSG00000105732	Chromatin interaction
ENSG00000167619	Chromatin interaction
ENSG00000105723	Chromatin interaction
ENSG00000105429	Chromatin interaction
ENSG00000167625	Chromatin interaction
ENSG00000213904	Chromatin interaction
ENSG00000079432	Chromatin interaction
ENSG00000076928	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10410185	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10410198	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10410698	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10412833	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10426306	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10426310	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11557114	0.82[ASN][1000 genomes]
rs11878620	0.82[CHB][hapmap];0.82[ASN][1000 genomes]
rs11880124	0.82[CHB][hapmap]
rs11882654	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11883412	0.82[CHB][hapmap]
rs1206009	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1206027	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.91[LWK][hapmap];0.90[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1206028	1.00[ASW][hapmap];0.85[GIH][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];0.85[TSI][hapmap];0.95[YRI][hapmap];0.82[AMR][1000 genomes]
rs1206029	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.80[MEX][hapmap];0.94[TSI][hapmap];0.81[EUR][1000 genomes]
rs1206031	0.82[EUR][1000 genomes]
rs1206033	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.89[MEX][hapmap];0.89[TSI][hapmap]
rs1206035	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1206038	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.88[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1206040	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1206041	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.88[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1206042	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1206043	0.84[EUR][1000 genomes]
rs1206044	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[YRI][hapmap];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1209280	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1211265	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13346991	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1613100	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.87[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];0.94[TSI][hapmap];0.95[YRI][hapmap];0.84[EUR][1000 genomes]
rs1654623	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.90[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];0.94[TSI][hapmap];0.95[YRI][hapmap];0.84[EUR][1000 genomes]
rs1676211	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.88[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1676213	0.84[EUR][1000 genomes]
rs1676215	0.84[EUR][1000 genomes]
rs1676217	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1676220	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1676221	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1676222	1.00[CHB][hapmap]
rs1685565	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes]
rs16975684	0.82[CHB][hapmap]
rs2267630	1.00[CHB][hapmap]
rs2302485	0.82[CHB][hapmap];0.82[ASN][1000 genomes]
rs2303652	0.82[CHB][hapmap]
rs2615614	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28537976	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28621009	1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[TSI][hapmap];0.82[EUR][1000 genomes]
rs34922891	0.81[EUR][1000 genomes]
rs35493131	0.82[ASN][1000 genomes]
rs35557987	0.82[EUR][1000 genomes]
rs3745231	0.82[CHB][hapmap]
rs3745233	0.82[CHB][hapmap]
rs3810148	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.80[MEX][hapmap];0.94[TSI][hapmap];0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs3810151	0.82[CHB][hapmap]
rs4141062	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs57938324	0.90[ASN][1000 genomes]
rs61995685	0.81[EUR][1000 genomes]
rs7248379	0.82[CHB][hapmap]
rs7255956	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7258795	0.90[ASN][1000 genomes]
rs7260287	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73552881	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73552895	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs741070	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs8182491	0.82[CHB][hapmap]
rs851292	0.81[EUR][1000 genomes]
rs851293	0.81[EUR][1000 genomes]
rs851296	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.87[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];0.94[TSI][hapmap];0.89[YRI][hapmap];0.84[EUR][1000 genomes]
rs851612	0.86[ASN][1000 genomes]
rs851615	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs862228	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs865436	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9636121	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.89[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv520239	chr19:42357455-42931004	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv911782	chr19:42514712-42931004	Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
4	nsv1055554	chr19:42619671-42821642	Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
5	nsv526186	chr19:42676481-43203507	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
6	esv2422471	chr19:42733141-43669485	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
7	nsv833834	chr19:42736444-42835027	Genic enhancers Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	42 gene(s)	inside rSNPs	diseases
8	nsv911785	chr19:42741124-42917545	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42805800-42807400	Flanking Active TSS	Primary B cells from cord blood	blood
2	chr19:42805800-42807400	Flanking Active TSS	Primary hematopoietic stem cells	blood
3	chr19:42805800-42807400	Active TSS	Brain Angular Gyrus	brain
4	chr19:42805800-42807400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr19:42805800-42807800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
6	chr19:42806000-42807400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr19:42806000-42807400	Active TSS	Fetal Kidney	kidney
8	chr19:42806000-42808000	Active TSS	Rectal Smooth Muscle	rectum
9	chr19:42806200-42807400	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr19:42806200-42807400	Active TSS	NHLF	lung
11	chr19:42806200-42807800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr19:42806400-42807400	Active TSS	Brain Substantia Nigra	brain
13	chr19:42806600-42807400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr19:42806600-42807400	Active TSS	Fetal Brain Female	brain
15	chr19:42806600-42807400	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr19:42806600-42807600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr19:42806600-42807600	Enhancers	Fetal Heart	heart
18	chr19:42806800-42807400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr19:42806800-42807400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
20	chr19:42806800-42807400	Active TSS	Brain Germinal Matrix	brain
21	chr19:42806800-42807400	Enhancers	Lung	lung
22	chr19:42806800-42807400	Weak transcription	Small Intestine	intestine
23	chr19:42806800-42807600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr19:42806800-42807600	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr19:42806800-42807600	Flanking Active TSS	Dnd41	blood
26	chr19:42806800-42808000	Enhancers	Spleen	Spleen
27	chr19:42807000-42807400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr19:42807000-42807400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
29	chr19:42807000-42807400	Flanking Active TSS	Primary B cells from peripheral blood	blood
30	chr19:42807000-42807400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
31	chr19:42807000-42807400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr19:42807000-42807400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
33	chr19:42807000-42807400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr19:42807000-42807400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
35	chr19:42807000-42807400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr19:42807000-42807400	Flanking Active TSS	Fetal Muscle Leg	muscle
37	chr19:42807000-42807400	Flanking Active TSS	Fetal Thymus	thymus
38	chr19:42807000-42807400	Weak transcription	Gastric	stomach
39	chr19:42807000-42807400	Flanking Active TSS	Stomach Mucosa	stomach
40	chr19:42807000-42807400	Flanking Active TSS	HMEC	breast
41	chr19:42807000-42807400	Flanking Active TSS	NH-A	brain
42	chr19:42807000-42807400	Flanking Active TSS	NHEK	skin
43	chr19:42807000-42807600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr19:42807000-42807600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr19:42807000-42807600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr19:42807000-42807600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chr19:42807000-42807600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr19:42807000-42807600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr19:42807000-42807600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr19:42807000-42807600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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