Variant report

Variant	rs16891464
Chromosome Location	chr6:26235300-26235301
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:183)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:26233532-26235480	HUVEC	blood vessel:	n/a	n/a
2	NRF1	chr6:26233287-26235329	H1-hESC	embryonic stem cell:	n/a	n/a
3	SP1	chr6:26234720-26235517	H1-hESC	embryonic stem cell:	n/a	n/a
4	NFYA	chr6:26235060-26235681	GM12878	blood:	n/a	chr6:26235260-26235275 chr6:26235256-26235274 chr6:26235263-26235273
5	CREB1	chr6:26233019-26235417	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr6:26232959-26235359	SK-N-SH	brain:	n/a	n/a
7	SP4	chr6:26232935-26235412	H1-hESC	embryonic stem cell:	n/a	n/a
8	TBL1XR1	chr6:26233211-26235346	K562	blood:	n/a	n/a
9	YY1	chr6:26234859-26235338	H1-hESC	embryonic stem cell:	n/a	n/a
10	HEY1	chr6:26232360-26235431	K562	blood:	n/a	n/a
11	CHD2	chr6:26232930-26235320	K562	blood:	n/a	n/a
12	POLR2A	chr6:26233043-26235359	GM12878	blood:	n/a	n/a
13	POLR2A	chr6:26233282-26235338	A549	lung:	n/a	n/a
14	POLR2A	chr6:26234798-26235318	HUVEC	blood vessel:	n/a	n/a
15	ELF1	chr6:26233305-26235353	GM12878	blood:	n/a	n/a
16	E2F6	chr6:26235184-26235368	K562	blood:	n/a	n/a
17	CTCF	chr6:26235257-26235321	GM19240	blood:	n/a	n/a
18	POLR2A	chr6:26232386-26235514	GM12878	blood:	n/a	n/a
19	POLR2A	chr6:26233560-26235322	A549	lung:	n/a	n/a
20	UBTF	chr6:26234398-26235397	K562	blood:	n/a	n/a
21	PBX3	chr6:26233778-26235315	A549	lung:	n/a	n/a
22	BCLAF1	chr6:26233509-26235413	GM12878	blood:	n/a	chr6:26234372-26234385 chr6:26234308-26234316
23	CHD1	chr6:26233057-26235307	GM12878	blood:	n/a	n/a
24	CBX3	chr6:26234741-26235363	K562	blood:	n/a	n/a
25	CHD2	chr6:26232706-26235433	H1-hESC	embryonic stem cell:	n/a	n/a
26	NFIC	chr6:26233580-26235402	GM12878	blood:	n/a	n/a
27	RELA	chr6:26233850-26235358	GM18951	blood:	n/a	n/a
28	POLR2A	chr6:26230664-26235434	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr6:26232363-26235719	MCF-7	breast:	n/a	n/a
30	ZNF384	chr6:26233138-26235373	GM12878	blood:	n/a	n/a
31	ETS1	chr6:26234996-26235318	A549	lung:	n/a	n/a
32	POLR2A	chr6:26233185-26235395	GM12891	blood:	n/a	n/a
33	BCL3	chr6:26233671-26235329	A549	lung:	n/a	chr6:26234372-26234385 chr6:26234308-26234316
34	TAF7	chr6:26231102-26235460	H1-hESC	embryonic stem cell:	n/a	n/a
35	PBX3	chr6:26234753-26235433	SK-N-SH	brain:	n/a	n/a
36	POLR2A	chr6:26233170-26235360	GM12878	blood:	n/a	n/a
37	MXI1	chr6:26232890-26235546	IMR90	lung:	n/a	n/a
38	POLR2A	chr6:26232620-26235395	GM19099	blood:	n/a	n/a
39	MTA3	chr6:26233584-26235377	GM12878	blood:	n/a	n/a
40	POLR2A	chr6:26232125-26235418	H1-hESC	embryonic stem cell:	n/a	n/a
41	SIN3AK20	chr6:26233783-26235351	K562	blood:	n/a	n/a
42	RELA	chr6:26233531-26235347	GM19099	blood:	n/a	n/a
43	NFYB	chr6:26235012-26235564	GM12878	blood:	n/a	chr6:26235260-26235275 chr6:26235263-26235273
44	ZBTB33	chr6:26233143-26235551	SK-N-SH	brain:	n/a	chr6:26235409-26235418 chr6:26235491-26235500
45	POLR2A	chr6:26233705-26235397	A549	lung:	n/a	n/a
46	POLR2A	chr6:26233113-26235414	GM12891	blood:	n/a	n/a
47	TCF12	chr6:26234653-26235344	A549	lung:	n/a	n/a
48	KAP1	chr6:26234904-26235322	U2OS	brain:	n/a	n/a
49	POLR2A	chr6:26233219-26235395	GM19193	blood:	n/a	n/a
50	POLR2A	chr6:26233148-26235443	GM12891	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26235287-26235337	PANC-1	pancreas:	n/a
2	chr6:26235254-26235304	HMEC	breast:	n/a
3	chr6:26235254-26235304	AoSMC	blood vessel:	n/a
4	chr6:26235287-26235337	GM19239	blood:	n/a
5	chr6:26235287-26235337	GM12891	blood:	n/a
6	chr6:26235287-26235337	NB4	blood:	n/a
7	chr6:26235290-26235340	AG09319	gingival:	n/a
8	chr6:26235254-26235304	ProgFib	skin:	n/a
9	chr6:26235254-26235304	SKMC	muscle:	n/a
10	chr6:26235254-26235304	AG04449	skin:	fetal
11	chr6:26235287-26235337	AG10803	skin:	n/a
12	chr6:26235254-26235304	IMR90	lung:	fetal
13	chr6:26235254-26235304	NHDF-neo	bronchial:	n/a
14	chr6:26235287-26235337	AG04449	skin:	fetal
15	chr6:26235290-26235340	HMEC	breast:	n/a
16	chr6:26235290-26235340	ovcar-3	ovarian:	n/a
17	chr6:26235287-26235337	SKMC	muscle:	n/a
18	chr6:26235287-26235337	HRE	kidney:	n/a
19	chr6:26235290-26235340	PFSK-1	brain:	n/a
20	chr6:26235290-26235340	HRPEpiC	eye:	n/a
21	chr6:26235290-26235340	HCT-116	colon:	n/a
22	chr6:26235287-26235337	GM06990	blood:	n/a
23	chr6:26235287-26235337	ovcar-3	ovarian:	n/a
24	chr6:26235287-26235337	AG09309	skin:	n/a
25	chr6:26235254-26235304	BJ	skin:	n/a
26	chr6:26235287-26235337	NT2-D1	testis:	n/a
27	chr6:26235290-26235340	LNCaP	prostate:	n/a
28	chr6:26235287-26235337	BE2_C	brain:	n/a
29	chr6:26235290-26235340	MCF10A-Er-Src	breast:	n/a
30	chr6:26235290-26235340	AG10803	skin:	n/a
31	chr6:26235287-26235337	Hepatocyte	liver:	n/a
32	chr6:26235290-26235340	Caco-2	colon:	n/a
33	chr6:26235254-26235304	HRE	kidney:	n/a
34	chr6:26235254-26235304	T-47D	breast:	n/a
35	chr6:26235254-26235304	HNPCEpiC	eye:	n/a
36	chr6:26235290-26235340	U87	brain:	n/a
37	chr6:26235287-26235337	HRCEpiC	kidney:	n/a
38	chr6:26235254-26235304	NH-A	brain:	n/a
39	chr6:26235290-26235340	HEK293	kidney:	embryo
40	chr6:26235254-26235304	HCM	heart:	n/a
41	chr6:26235254-26235304	K562	blood:	n/a
42	chr6:26235254-26235304	SK-N-MC	brain:	n/a
43	chr6:26235287-26235337	GM12892	blood:	n/a
44	chr6:26235254-26235304	Hela-S3	cervix:	n/a
45	chr6:26235290-26235340	SK-N-SH_RA	brain:	n/a
46	chr6:26235254-26235304	H1-hESC	embryonic stem cell:	embryo
47	chr6:26235287-26235337	SK-N-SH_RA	brain:	n/a
48	chr6:26235287-26235337	HepG2	liver:	n/a
49	chr6:26235254-26235304	HUVEC	blood vessel:	n/a
50	chr6:26235254-26235304	ovcar-3	ovarian:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26233448..26235462-chr6:27099272..27101626,2	MCF-7	breast:
2	chr16:33963952..33966447-chr6:26233532..26235518,2	MCF-7	breast:
3	chr6:26233018..26235518-chr6:27781228..27784528,3	MCF-7	breast:
4	chr1:145469949..145470604-chr6:26234575..26235468,2	NB4	blood:
5	chr6:24719968..24721731-chr6:26234799..26237042,2	K562	blood:
6	chr6:26031185..26034143-chr6:26233658..26236359,2	MCF-7	breast:
7	chr6:26225043..26225693-chr6:26235156..26235831,2	MCF-7	breast:
8	chr11:62608417..62609626-chr6:26234563..26235451,4	NB4	blood:
9	chr6:26232392..26235722-chr6:27100798..27102386,3	K562	blood:
10	chr6:26231234..26236589-chr6:27099738..27104932,8	K562	blood:
11	chr17:56736343..56738004-chr6:26233634..26236262,2	MCF-7	breast:
12	chr15:65425945..65426715-chr6:26234552..26235534,2	NB4	blood:
13	chr6:26020523..26023508-chr6:26233779..26236758,2	MCF-7	breast:
14	chr15:74753352..74756015-chr6:26233514..26236458,2	K562	blood:
15	chr3:28388905..28390597-chr6:26234908..26237633,2	K562	blood:
16	chr6:26234528..26236146-chr6:26520612..26523386,2	K562	blood:
17	chr6:26233781..26236628-chr6:27113286..27115220,2	K562	blood:
18	chr16:2009340..2011468-chr6:26233811..26235989,2	MCF-7	breast:

No data

Variant related genes	Relation type
HIST1H1D	TF binding region
HIST1H1D	CpG island
ENSG00000121851	Chromatin interaction
ENSG00000163512	Chromatin interaction
ENSG00000200434	Chromatin interaction
ENSG00000247240	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000112308	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000196374	Chromatin interaction
ENSG00000140990	Chromatin interaction
ENSG00000090470	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000181039	Chromatin interaction
ENSG00000196966	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000182611	Chromatin interaction
ENSG00000138629	Chromatin interaction
ENSG00000196176	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11751062	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11751286	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11751812	1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs11753084	0.83[EUR][1000 genomes]
rs11753610	1.00[CHD][hapmap];0.91[GIH][hapmap]
rs11753717	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11753837	1.00[ASW][hapmap];0.87[GIH][hapmap];0.94[LWK][hapmap];0.85[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11754140	0.87[EUR][1000 genomes]
rs11754368	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11755618	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11757549	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];0.84[LWK][hapmap];0.96[MKK][hapmap];0.87[TSI][hapmap];0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11757724	0.86[EUR][1000 genomes]
rs11759758	0.85[EUR][1000 genomes]
rs11760140	0.82[EUR][1000 genomes]
rs16891375	1.00[TSI][hapmap];0.85[EUR][1000 genomes]
rs16891407	0.87[EUR][1000 genomes]
rs16891484	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1981019	0.85[EUR][1000 genomes]
rs2179516	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3734534	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MKK][hapmap];0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs41266811	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56119218	0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61746493	0.83[AFR][1000 genomes]
rs61978632	0.80[AFR][1000 genomes]
rs7775052	1.00[ASW][hapmap];0.87[GIH][hapmap];0.94[LWK][hapmap];0.85[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
8	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
9	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
10	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
11	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
12	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
13	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
14	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
15	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases
16	nsv1021294	chr6:26190316-26246784	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	309 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs16891464	HIST1H3E	Cis_1M	lymphoblastoid	RTeQTL
rs16891464	HIST1H2AE	cis	multi-tissue	Pritchard

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26231200-26236000	Active TSS	Thymus	Thymus
2	chr6:26232400-26236000	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr6:26232600-26235800	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr6:26232800-26235400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr6:26232800-26235600	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr6:26232800-26235600	Active TSS	Aorta	Aorta
7	chr6:26232800-26235800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr6:26232800-26235800	Active TSS	Fetal Lung	lung
9	chr6:26233000-26235400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:26233000-26235600	Active TSS	Primary T killer memory cells from peripheral blood	blood
11	chr6:26233000-26235800	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr6:26233000-26235800	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr6:26233000-26235800	Bivalent/Poised TSS	Brain Angular Gyrus	brain
14	chr6:26233000-26236000	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr6:26233000-26236000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:26233200-26235400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:26233200-26235400	Active TSS	Esophagus	oesophagus
18	chr6:26233200-26235400	Active TSS	Rectal Mucosa Donor 29	rectum
19	chr6:26233200-26235400	Transcr. at gene 5' and 3'	Right Atrium	heart
20	chr6:26233200-26235600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr6:26233200-26235600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
22	chr6:26233200-26235600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
23	chr6:26233200-26235600	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
24	chr6:26233200-26235600	Bivalent/Poised TSS	Psoas Muscle	Psoas
25	chr6:26233200-26235800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr6:26233200-26235800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr6:26233200-26235800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:26233200-26235800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr6:26233200-26235800	Active TSS	Fetal Stomach	stomach
30	chr6:26233200-26235800	Active TSS	Rectal Smooth Muscle	rectum
31	chr6:26233200-26235800	Flanking Active TSS	HUVEC	blood vessel
32	chr6:26233200-26235800	Active TSS	NHLF	lung
33	chr6:26233200-26236000	Active TSS	Fetal Kidney	kidney
34	chr6:26233200-26236000	Active TSS	A549	lung
35	chr6:26233400-26235400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:26233400-26235600	Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr6:26233400-26235600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:26233400-26235800	Active TSS	H9 Cell Line	embryonic stem cell
39	chr6:26233600-26235800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:26233600-26235800	Active TSS	Fetal Intestine Small	intestine
41	chr6:26233600-26235800	Bivalent/Poised TSS	NHDF-Ad	bronchial
42	chr6:26233600-26236000	Active TSS	H1 Cell Line	embryonic stem cell
43	chr6:26233800-26235400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
44	chr6:26233800-26235400	Flanking Active TSS	Liver	Liver
45	chr6:26233800-26235600	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:26233800-26235600	Active TSS	Primary T cells from cord blood	blood
47	chr6:26233800-26235600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr6:26233800-26235600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
49	chr6:26233800-26235800	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr6:26233800-26235800	Active TSS	Fetal Heart	heart

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