Variant report

Variant	rs2291617
Chromosome Location	chr12:58166403-58166404
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:273)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TBP	chr12:58165192-58167114	K562	blood:	n/a	n/a
2	MXI1	chr12:58164482-58167187	IMR90	lung:	n/a	chr12:58164814-58164829
3	POLR2A	chr12:58165457-58166975	K562	blood:	n/a	n/a
4	POLR2A	chr12:58165461-58166630	HCT-116	colon:	n/a	n/a
5	POLR2A	chr12:58165178-58166833	HL-60	blood:	n/a	n/a
6	MAX	chr12:58165288-58167068	HepG2	liver:	n/a	chr12:58166431-58166441
7	YY1	chr12:58165484-58166583	ECC-1	luminal epithelium:	n/a	chr12:58166470-58166484 chr12:58166314-58166325
8	TAF1	chr12:58165480-58166732	SK-N-SH	brain:	n/a	n/a
9	POLR2A	chr12:58165031-58166990	Hela-S3	cervix:	n/a	n/a
10	CEBPD	chr12:58165647-58166613	HepG2	liver:	n/a	n/a
11	YY1	chr12:58165402-58166825	HepG2	liver:	n/a	chr12:58166470-58166484 chr12:58166314-58166325
12	RCOR1	chr12:58165382-58166893	Hela-S3	cervix:	n/a	n/a
13	RFX5	chr12:58165404-58166918	Hela-S3	cervix:	n/a	n/a
14	MTA3	chr12:58165193-58167077	GM12878	blood:	n/a	n/a
15	POLR2A	chr12:58165205-58166952	PFSK-1	brain:	n/a	n/a
16	POLR2A	chr12:58165230-58166809	GM15510	blood:	n/a	n/a
17	POLR2A	chr12:58165126-58166925	IMR90	lung:	n/a	n/a
18	POLR2A	chr12:58165120-58166916	GM12891	blood:	n/a	n/a
19	ELF1	chr12:58165519-58166641	MCF-7	breast:	n/a	chr12:58166317-58166329
20	CREB1	chr12:58165141-58167012	HepG2	liver:	n/a	chr12:58165632-58165645
21	SIN3AK20	chr12:58165438-58166603	PANC-1	pancreas:	n/a	n/a
22	ZNF263	chr12:58165233-58166795	HEK293-T-REx	kidney:	n/a	chr12:58166368-58166377
23	SMARCC1	chr12:58165234-58167014	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr12:58165544-58166549	HepG2	liver:	n/a	n/a
25	JUND	chr12:58165249-58167042	K562	blood:	n/a	chr12:58165634-58165643 chr12:58166387-58166396
26	TCF12	chr12:58164990-58166916	A549	lung:	n/a	chr12:58165412-58165419
27	POLR2A	chr12:58164350-58167067	K562	blood:	n/a	n/a
28	TAF1	chr12:58165430-58166680	PFSK-1	brain:	n/a	n/a
29	HDAC2	chr12:58166401-58166820	HepG2	liver:	n/a	n/a
30	SIN3AK20	chr12:58165273-58166526	A549	lung:	n/a	n/a
31	POLR2A	chr12:58165520-58166539	A549	lung:	n/a	n/a
32	POLR2A	chr12:58165311-58166981	K562	blood:	n/a	n/a
33	MXI1	chr12:58165377-58166991	HepG2	liver:	n/a	n/a
34	CUX1	chr12:58165286-58166466	K562	blood:	n/a	n/a
35	POLR2A	chr12:58165086-58167033	K562	blood:	n/a	n/a
36	RCOR1	chr12:58165470-58166639	HepG2	liver:	n/a	n/a
37	POLR2A	chr12:58165256-58166916	SK-N-SH	brain:	n/a	n/a
38	SIN3AK20	chr12:58165256-58166841	MCF-7	breast:	n/a	n/a
39	POLR2A	chr12:58165140-58166761	GM12892	blood:	n/a	n/a
40	TCF7L2	chr12:58165423-58166758	Hela-S3	cervix:	n/a	n/a
41	YY1	chr12:58165418-58166978	K562	blood:	n/a	chr12:58166470-58166484 chr12:58166314-58166325
42	POLR2A	chr12:58165409-58166806	ProgFib	skin:	n/a	n/a
43	POLR2A	chr12:58165441-58166755	HUVEC	blood vessel:	n/a	n/a
44	POLR2A	chr12:58165148-58166902	HepG2	liver:	n/a	n/a
45	E2F6	chr12:58165699-58166633	A549	lung:	n/a	chr12:58165955-58165967 chr12:58166388-58166397 chr12:58166319-58166331
46	MAX	chr12:58165533-58166810	HUVEC	blood vessel:	n/a	chr12:58166431-58166441
47	ZEB1	chr12:58165915-58166426	GM12878	blood:	n/a	chr12:58166178-58166185 chr12:58166160-58166171
48	POLR2A	chr12:58165172-58167055	U87	brain:	n/a	n/a
49	MAX	chr12:58165159-58167088	ECC-1	luminal epithelium:	n/a	chr12:58166431-58166441
50	KAP1	chr12:58165454-58166813	HEK293	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:58166393-58166443	NHBE	bronchial:	n/a
2	chr12:58166393-58166443	PrEC	prostate:	n/a
3	chr12:58166393-58166443	NH-A	brain:	n/a
4	chr12:58166393-58166443	A549	lung:	n/a
5	chr12:58166393-58166443	ECC-1	luminal epithelium:	n/a
6	chr12:58166393-58166443	GM06990	blood:	n/a
7	chr12:58166393-58166443	T-47D	breast:	n/a
8	chr12:58166393-58166443	GM12892	blood:	n/a
9	chr12:58166393-58166443	Hela-S3	cervix:	n/a
10	chr12:58166393-58166443	HCT-116	colon:	n/a
11	chr12:58166393-58166443	HL-60	blood:	n/a
12	chr12:58166393-58166443	HIPEpiC	eye:	n/a
13	chr12:58166393-58166443	NT2-D1	testis:	n/a
14	chr12:58166393-58166443	AoSMC	blood vessel:	n/a
15	chr12:58166393-58166443	GM12891	blood:	n/a
16	chr12:58166393-58166443	HCF	heart:	n/a
17	chr12:58166393-58166443	GM12878	blood:	n/a
18	chr12:58166393-58166443	PANC-1	pancreas:	n/a
19	chr12:58166393-58166443	SK-N-SH_RA	brain:	n/a
20	chr12:58166393-58166443	K562	blood:	n/a
21	chr12:58166393-58166443	BE2_C	brain:	n/a
22	chr12:58166393-58166443	Hepatocyte	liver:	n/a
23	chr12:58166393-58166443	HAEpiC	amniotic membrane:	n/a
24	chr12:58166393-58166443	IMR90	lung:	fetal
25	chr12:58166393-58166443	AG04449	skin:	fetal
26	chr12:58166393-58166443	HCM	heart:	n/a
27	chr12:58166393-58166443	SK-N-SH	brain:	n/a
28	chr12:58166393-58166443	HMEC	breast:	n/a
29	chr12:58166393-58166443	HNPCEpiC	eye:	n/a
30	chr12:58166393-58166443	ovcar-3	ovarian:	n/a
31	chr12:58166393-58166443	SKMC	muscle:	n/a
32	chr12:58166393-58166443	Jurkat	blood:	n/a
33	chr12:58166393-58166443	NHDF-neo	bronchial:	n/a
34	chr12:58166393-58166443	HepG2	liver:	n/a
35	chr12:58166393-58166443	ProgFib	skin:	n/a
36	chr12:58166393-58166443	NB4	blood:	n/a
37	chr12:58166393-58166443	PFSK-1	brain:	n/a
38	chr12:58166393-58166443	HCPEpiC	choroid plexus:	n/a
39	chr12:58166393-58166443	AG10803	skin:	n/a
40	chr12:58166393-58166443	MCF10A-Er-Src	breast:	n/a
41	chr12:58166393-58166443	HUVEC	blood vessel:	n/a
42	chr12:58166393-58166443	AG04450	lung:	fetal
43	chr12:58166393-58166443	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:58166393-58166443	Caco-2	colon:	n/a
45	chr12:58166393-58166443	AG09309	skin:	n/a
46	chr12:58166393-58166443	MCF-7	breast:	n/a
47	chr12:58166393-58166443	HRE	kidney:	n/a
48	chr12:58166393-58166443	U87	brain:	n/a
49	chr12:58166393-58166443	SAEC	small airway:	n/a
50	chr12:58166393-58166443	LNCaP	prostate:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:58166150..58166770-chr6:30710132..30711087,2	Hela-S3	cervix:
2	chr12:58166094..58167924-chr12:58290124..58292095,2	MCF-7	breast:
3	chr12:58163238..58167741-chr12:58238267..58242135,5	MCF-7	breast:
4	chr1:147806754..147807358-chr12:58165991..58166519,2	Hela-S3	cervix:
5	chr12:57632502..57635395-chr12:58164755..58167639,2	MCF-7	breast:
6	chr12:58165655..58167905-chr12:58237563..58240125,2	K562	blood:
7	chr12:58166254..58167194-chr16:2731844..2732719,2	Hela-S3	cervix:
8	chr12:58015127..58017483-chr12:58164900..58167382,2	K562	blood:
9	chr12:58164678..58167264-chr12:58237471..58241552,5	MCF-7	breast:
10	chr12:58165555..58166512-chr12:58175671..58176492,3	K562	blood:
11	chr12:58164479..58167905-chr12:58237563..58242209,7	K562	blood:
12	chr12:58165699..58166613-chr17:25621025..25621834,2	Hela-S3	cervix:
13	chr12:58165013..58167189-chr3:185654127..185656713,2	MCF-7	breast:
14	chr12:58015983..58018978-chr12:58164900..58166825,2	K562	blood:
15	chr12:57823258..57825830-chr12:58164419..58166506,2	MCF-7	breast:
16	chr12:58165725..58168554-chr12:58208746..58212137,3	MCF-7	breast:
17	chr12:58087206..58088752-chr12:58165817..58167834,2	MCF-7	breast:
18	chr12:58164836..58167188-chr12:58333922..58337646,3	K562	blood:
19	chr12:58004396..58008788-chr12:58163385..58167140,4	MCF-7	breast:
20	chr12:57911596..57914324-chr12:58165059..58166579,2	MCF-7	breast:
21	chr12:58164894..58167465-chr12:58198689..58202991,3	K562	blood:
22	chr12:57913372..57915977-chr12:58164344..58168645,6	K562	blood:
23	chr12:58165030..58167398-chr12:58198100..58200821,2	MCF-7	breast:
24	chr12:58164032..58167803-chr12:58328284..58330655,5	K562	blood:
25	chr12:57912814..57915992-chr12:58164344..58170030,6	K562	blood:
26	chr12:58165907..58166669-chr6:52441299..52441930,2	Hela-S3	cervix:
27	chr12:58165740..58166574-chr12:58176461..58177013,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
ENSG00000257921	TF binding region
METTL21B	TF binding region
METTL1	TF binding region
CYP27B1	TF binding region
ENSG00000257921	CpG island
METTL21B	CpG island
METTL1	CpG island
CYP27B1	CpG island
ENSG00000135502	Chromatin interaction
ENSG00000208028	Chromatin interaction
ENSG00000257698	Chromatin interaction
ENSG00000206749	Chromatin interaction
ENSG00000167977	Chromatin interaction
ENSG00000245651	Chromatin interaction
ENSG00000185633	Chromatin interaction
ENSG00000137312	Chromatin interaction
ENSG00000272273	Chromatin interaction
ENSG00000240771	Chromatin interaction
ENSG00000166896	Chromatin interaction
ENSG00000135506	Chromatin interaction
ENSG00000109046	Chromatin interaction
ENSG00000175197	Chromatin interaction
ENSG00000065308	Chromatin interaction
ENSG00000166987	Chromatin interaction
ENSG00000202408	Chromatin interaction
ENSG00000258001	Chromatin interaction
ENSG00000123297	Chromatin interaction
ENSG00000136527	Chromatin interaction
ENSG00000135407	Chromatin interaction
ENSG00000179912	Chromatin interaction
ENSG00000175215	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 21 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1021469	0.92[CEU][hapmap];0.81[TSI][hapmap];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10431505	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10431552	1.00[CEU][hapmap];0.94[TSI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10747783	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10783847	1.00[CEU][hapmap];0.94[TSI][hapmap];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10783848	1.00[CEU][hapmap];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10877011	0.85[CEU][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs10877012	1.00[CEU][hapmap];0.94[TSI][hapmap];0.82[YRI][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10877013	0.96[CEU][hapmap];0.94[TSI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10877014	1.00[CEU][hapmap];0.94[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10877015	1.00[CEU][hapmap];0.94[TSI][hapmap];0.82[YRI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10877016	0.90[ASW][hapmap];1.00[CEU][hapmap];0.82[LWK][hapmap];0.94[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10877017	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10877018	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10877019	1.00[CEU][hapmap];0.94[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11172333	1.00[CEU][hapmap];0.94[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11172335	1.00[CEU][hapmap];0.94[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11172342	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11172343	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11172344	1.00[CEU][hapmap];0.94[TSI][hapmap];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11172349	1.00[CEU][hapmap];0.94[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11172350	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11172351	1.00[CEU][hapmap];0.94[TSI][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1599932	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1875124	1.00[CEU][hapmap];0.94[TSI][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2014886	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2069502	1.00[CEU][hapmap];0.91[TSI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2069506	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2072052	1.00[CEU][hapmap];0.91[TSI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3782130	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3825079	1.00[CEU][hapmap];0.94[TSI][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4646536	1.00[CEU][hapmap];0.94[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56177740	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6581155	1.00[CEU][hapmap];0.94[TSI][hapmap]
rs703842	1.00[CEU][hapmap];0.94[TSI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs724834	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7965287	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8181644	1.00[CEU][hapmap];0.81[MKK][hapmap];0.94[TSI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs923829	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9652011	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038741	chr12:57877355-58174506	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
2	nsv541503	chr12:57877355-58174506	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
3	nsv899121	chr12:58079825-58177292	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv470296	chr12:58112189-58177292	Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
5	nsv510601	chr12:58130298-58191925	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
6	nsv470297	chr12:58133256-58202419	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
7	nsv559046	chr12:58162085-58478598	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	261 gene(s)	inside rSNPs	diseases

mRNA abundance (count:21)

SNP	Gene	Cis/trans	Tissue	Source
rs2291617	TSFM	Cis_1M	lymphoblastoid	RTeQTL
rs2291617	METTL21B	cis	Adipose Subcutaneous	GTEx
rs2291617	METTL21B	cis	Skin Sun Exposed Lower leg	GTEx
rs2291617	TSFM	cis	multi-tissue	Pritchard
rs2291617	METTL21B	cis	lung	GTEx
rs2291617	FAM119B	cis	Cerebellum	GTEx
rs2291617	FAM119B	cis	Frontal Cortex	GTEx
rs2291617	FAM119B	Cis_1M	lymphoblastoid	RTeQTL
rs2291617	CYP27B1	cis	Thyroid	GTEx
rs2291617	METTL21B	cis	Heart Left Ventricle	GTEx
rs2291617	XRCC6BP1	cis	Muscle Skeletal	GTEx
rs2291617	METTL21B	cis	Whole Blood	GTEx
rs2291617	RP11-571M6.13	cis	Thyroid	GTEx
rs2291617	XRCC6BP1	cis	Whole Blood	GTEx
rs2291617	METTL21B	cis	Esophagus Mucosa	GTEx
rs2291617	TSFM	cis	Muscle Skeletal	GTEx
rs2291617	FAM119B	cis	Brain Pons	GTEx
rs2291617	DKFZP586D0919	cis	multi-tissue	Pritchard
rs2291617	METTL21B	cis	Muscle Skeletal	GTEx
rs2291617	FAM119B	cis	Lymphoblastoid	GTEx
rs2291617	METTL21B	cis	Esophagus Muscularis	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58164800-58167200	Active TSS	Psoas Muscle	Psoas
2	chr12:58164800-58167200	Active TSS	Right Ventricle	heart
3	chr12:58165000-58166800	Active TSS	K562	blood
4	chr12:58165000-58167000	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr12:58165000-58167000	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr12:58165000-58167200	Active TSS	H9 Cell Line	embryonic stem cell
7	chr12:58165000-58167200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:58165000-58167200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr12:58165000-58167200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:58165000-58167200	Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr12:58165000-58167200	Active TSS	Hela-S3	cervix
12	chr12:58165000-58167400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
13	chr12:58165000-58167400	Active TSS	Fetal Kidney	kidney
14	chr12:58165000-58167400	Active TSS	HSMMtube	muscle
15	chr12:58165000-58167800	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr12:58165200-58166600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
17	chr12:58165200-58166800	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr12:58165200-58166800	Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr12:58165200-58166800	Bivalent/Poised TSS	HepG2	liver
20	chr12:58165200-58167000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr12:58165200-58167200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr12:58165200-58167200	Active TSS	A549	lung
23	chr12:58165200-58167600	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr12:58165400-58166600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:58165400-58166600	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr12:58165400-58166600	Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr12:58165400-58166600	Active TSS	GM12878-XiMat	blood
28	chr12:58165400-58166800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:58165400-58166800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr12:58165400-58166800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr12:58165400-58166800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr12:58165400-58166800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr12:58165400-58166800	Active TSS	Rectal Smooth Muscle	rectum
34	chr12:58165400-58166800	Active TSS	Sigmoid Colon	Sigmoid Colon
35	chr12:58165400-58166800	Active TSS	Small Intestine	intestine
36	chr12:58165400-58167000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr12:58165400-58167000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr12:58165400-58167000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:58165400-58167000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
40	chr12:58165400-58167000	Active TSS	Aorta	Aorta
41	chr12:58165400-58167000	Active TSS	Esophagus	oesophagus
42	chr12:58165400-58167000	Active TSS	Fetal Intestine Large	intestine
43	chr12:58165400-58167000	Active TSS	Gastric	stomach
44	chr12:58165400-58167000	Active TSS	Left Ventricle	heart
45	chr12:58165400-58167000	Active TSS	HMEC	breast
46	chr12:58165400-58167200	Active TSS	H1 Cell Line	embryonic stem cell
47	chr12:58165400-58167200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr12:58165400-58167200	Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr12:58165400-58167200	Active TSS	Muscle Satellite Cultured Cells	--
50	chr12:58165400-58167200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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