Variant report

Variant	rs1056678
Chromosome Location	chr7:100860636-100860637
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	TAF1	chr7:100860405-100861166	K562	blood:	n/a	n/a
2	POLR2A	chr7:100860516-100861689	MCF-7	breast:	n/a	n/a
3	HEY1	chr7:100860495-100861687	K562	blood:	n/a	n/a
4	ELF1	chr7:100860065-100861977	MCF-7	breast:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
5	POLR2A	chr7:100860558-100861656	GM19193	blood:	n/a	n/a
6	CTCF	chr7:100860560-100860710	NHEK	skin:	n/a	n/a
7	ZBTB7A	chr7:100860137-100861098	ECC-1	luminal epithelium:	n/a	chr7:100860641-100860650
8	POLR2A	chr7:100860512-100861719	GM18951	blood:	n/a	n/a
9	RAD21	chr7:100860554-100861135	H1-hESC	embryonic stem cell:	n/a	n/a
10	MAX	chr7:100860060-100861813	Hela-S3	cervix:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
11	POLR2A	chr7:100860373-100861648	Gliobla	brain:	n/a	n/a
12	MXI1	chr7:100859501-100862549	IMR90	lung:	n/a	chr7:100861332-100861347
13	SIN3AK20	chr7:100859882-100862120	MCF-7	breast:	n/a	n/a
14	CTCF	chr7:100860526-100860733	NHEK	skin:	n/a	n/a
15	POLR2A	chr7:100859817-100863220	HepG2	liver:	n/a	n/a
16	YY1	chr7:100860429-100861628	K562	blood:	n/a	chr7:100861301-100861323 chr7:100861312-100861321
17	YY1	chr7:100860519-100861748	SK-N-SH_RA	brain:	n/a	chr7:100861301-100861323 chr7:100861312-100861321
18	RAD21	chr7:100860574-100860816	Hela-S3	cervix:	n/a	n/a
19	STAT5A	chr7:100860411-100861392	GM12878	blood:	n/a	n/a
20	THAP1	chr7:100860540-100861461	K562	blood:	n/a	chr7:100861298-100861322
21	CTCF	chr7:100860560-100860710	RPTEC	kidney:	n/a	n/a
22	ELF1	chr7:100860292-100861898	GM12878	blood:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
23	TAF1	chr7:100860538-100861093	K562	blood:	n/a	n/a
24	CTCF	chr7:100860500-100860650	GM12873	blood:	n/a	n/a
25	YY1	chr7:100860458-100861844	SK-N-SH	brain:	n/a	chr7:100861301-100861323 chr7:100861312-100861321
26	ETS1	chr7:100860254-100861192	K562	blood:	n/a	chr7:100860406-100860417
27	GABPA	chr7:100860582-100861622	K562	blood:	n/a	chr7:100861371-100861385 chr7:100861432-100861446 chr7:100861371-100861382 chr7:100861435-100861446 chr7:100861437-100861446
28	MYC	chr7:100860524-100861708	K562	blood:	n/a	chr7:100861338-100861347
29	POLR2A	chr7:100860455-100861653	K562	blood:	n/a	n/a
30	EGR1	chr7:100860587-100861626	MCF-7	breast:	n/a	chr7:100861288-100861297 chr7:100861517-100861530 chr7:100861372-100861381 chr7:100861436-100861445 chr7:100861395-100861404
31	CBX3	chr7:100859882-100862021	K562	blood:	n/a	n/a
32	YY1	chr7:100860580-100861843	SK-N-SH_RA	brain:	n/a	chr7:100861301-100861323 chr7:100861312-100861321
33	MYC	chr7:100860595-100861020	MCF10A-Er-Src	breast:	n/a	n/a
34	UBTF	chr7:100860104-100861180	K562	blood:	n/a	n/a
35	ZNF143	chr7:100860507-100861553	GM12878	blood:	n/a	n/a
36	SIN3AK20	chr7:100860513-100861879	A549	lung:	n/a	n/a
37	ETS1	chr7:100860324-100861607	K562	blood:	n/a	chr7:100861395-100861404 chr7:100861289-100861300 chr7:100861395-100861404 chr7:100861288-100861297 chr7:100860406-100860417 chr7:100861288-100861297 chr7:100861288-100861299 chr7:100861395-100861404 chr7:100861391-100861407 chr7:100861288-100861297 chr7:100861288-100861297 chr7:100861289-100861299 chr7:100861395-100861404 chr7:100861396-100861406 chr7:100861288-100861297 chr7:100861395-100861404 chr7:100861395-100861404 chr7:100861392-100861405 chr7:100861395-100861404 chr7:100861284-100861300
38	POLR2A	chr7:100860429-100861593	GM12878	blood:	n/a	n/a
39	CTCF	chr7:100860560-100860710	GM06990	blood:	n/a	n/a
40	POLR2A	chr7:100860009-100861708	MCF-7	breast:	n/a	n/a
41	YY1	chr7:100860549-100861743	GM12878	blood:	n/a	chr7:100861301-100861323 chr7:100861312-100861321
42	MAX	chr7:100859842-100861976	K562	blood:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
43	JUND	chr7:100860399-100861061	A549	lung:	n/a	chr7:100860559-100860568
44	TAF1	chr7:100860336-100861925	ECC-1	luminal epithelium:	n/a	n/a
45	NR2F2	chr7:100860493-100861622	K562	blood:	n/a	n/a
46	TCF12	chr7:100860255-100861637	ECC-1	luminal epithelium:	n/a	n/a
47	POLR2A	chr7:100860229-100861738	H1-neurons	neurons:	n/a	n/a
48	ELF1	chr7:100860394-100861913	MCF-7	breast:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
49	POLR2A	chr7:100860520-100861995	HepG2	liver:	n/a	n/a
50	E2F6	chr7:100859974-100861069	K562	blood:	n/a	chr7:100860148-100860159 chr7:100860306-100860321 chr7:100860334-100860349 chr7:100860132-100860143 chr7:100860304-100860314

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100860599-100860649	GM12878	blood:	n/a
2	chr7:100860599-100860649	AoSMC	blood vessel:	n/a
3	chr7:100860599-100860649	MCF10A-Er-Src	breast:	n/a
4	chr7:100860599-100860649	PFSK-1	brain:	n/a
5	chr7:100860599-100860649	HNPCEpiC	eye:	n/a
6	chr7:100860599-100860649	IMR90	lung:	fetal
7	chr7:100860599-100860649	ProgFib	skin:	n/a
8	chr7:100860599-100860649	HEEpiC	esophagus:	n/a
9	chr7:100860599-100860649	HepG2	liver:	n/a
10	chr7:100860599-100860649	HCM	heart:	n/a
11	chr7:100860599-100860649	T-47D	breast:	n/a
12	chr7:100860599-100860649	HL-60	blood:	n/a
13	chr7:100860599-100860649	Caco-2	colon:	n/a
14	chr7:100860599-100860649	Hela-S3	cervix:	n/a
15	chr7:100860599-100860649	NHBE	bronchial:	n/a
16	chr7:100860599-100860649	SAEC	small airway:	n/a
17	chr7:100860599-100860649	K562	blood:	n/a
18	chr7:100860599-100860649	AG09309	skin:	n/a
19	chr7:100860599-100860649	HMEC	breast:	n/a
20	chr7:100860599-100860649	HCF	heart:	n/a
21	chr7:100860599-100860649	SK-N-MC	brain:	n/a
22	chr7:100860599-100860649	H1-hESC	embryonic stem cell:	embryo
23	chr7:100860599-100860649	NHDF-neo	bronchial:	n/a
24	chr7:100860599-100860649	AG04449	skin:	fetal
25	chr7:100860599-100860649	HAEpiC	amniotic membrane:	n/a
26	chr7:100860599-100860649	PANC-1	pancreas:	n/a
27	chr7:100860599-100860649	HRPEpiC	eye:	n/a
28	chr7:100860599-100860649	HIPEpiC	eye:	n/a
29	chr7:100860599-100860649	GM19239	blood:	n/a
30	chr7:100860599-100860649	HRE	kidney:	n/a
31	chr7:100860599-100860649	HCPEpiC	choroid plexus:	n/a
32	chr7:100860599-100860649	NB4	blood:	n/a
33	chr7:100860599-100860649	HUVEC	blood vessel:	n/a
34	chr7:100860599-100860649	Jurkat	blood:	n/a
35	chr7:100860599-100860649	PrEC	prostate:	n/a
36	chr7:100860599-100860649	BJ	skin:	n/a
37	chr7:100860599-100860649	MCF-7	breast:	n/a
38	chr7:100860599-100860649	BE2_C	brain:	n/a
39	chr7:100860599-100860649	GM06990	blood:	n/a
40	chr7:100860599-100860649	Hepatocyte	liver:	n/a
41	chr7:100860599-100860649	NH-A	brain:	n/a
42	chr7:100860599-100860649	SKMC	muscle:	n/a
43	chr7:100860599-100860649	HRCEpiC	kidney:	n/a
44	chr7:100860599-100860649	GM12892	blood:	n/a
45	chr7:100860599-100860649	SK-N-SH_RA	brain:	n/a
46	chr7:100860599-100860649	A549	lung:	n/a
47	chr7:100860599-100860649	AG09319	gingival:	n/a
48	chr7:100860599-100860649	AG10803	skin:	n/a
49	chr7:100860599-100860649	LNCaP	prostate:	n/a
50	chr7:100860599-100860649	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:100859700..100862927-chr7:100863052..100866687,4	MCF-7	breast:
2	chr7:100730924..100734717-chr7:100859526..100862672,3	MCF-7	breast:
3	chr7:100860080..100860969-chr7:100887276..100888130,3	MCF-7	breast:
4	chr7:100859374..100863045-chr7:100885733..100890781,8	K562	blood:
5	chr7:100822622..100825395-chr7:100859780..100861285,2	K562	blood:
6	chr7:100859934..100861544-chr7:100949902..100952091,2	K562	blood:
7	chr7:100859513..100863025-chr7:100885730..100890155,10	MCF-7	breast:
8	chr7:100859404..100861068-chr7:100894037..100896793,2	MCF-7	breast:
9	chr7:100858946..100862708-chr7:100892771..100897292,5	MCF-7	breast:
10	chr7:100858331..100862020-chr7:100880126..100882464,3	K562	blood:
11	chr7:100808076..100812812-chr7:100858488..100864832,8	MCF-7	breast:
12	chr7:100860572..100862632-chr7:100892717..100896862,3	K562	blood:
13	chr7:100859409..100862433-chr7:100893851..100895703,4	K562	blood:
14	chr7:100858977..100861910-chr7:100881462..100883229,2	K562	blood:
15	chr7:100486477..100489401-chr7:100859928..100862607,2	MCF-7	breast:
16	chr7:100843889..100849523-chr7:100857776..100861352,9	MCF-7	breast:
17	chr7:100491458..100494589-chr7:100859109..100862606,4	MCF-7	breast:
18	chr7:100859877..100865511-chr7:100878168..100882490,7	MCF-7	breast:
19	chr7:100853413..100857189-chr7:100859048..100862216,5	K562	blood:
20	chr7:100858478..100862757-chr7:100884994..100890276,15	MCF-7	breast:
21	chr7:100853184..100857478-chr7:100859517..100863375,8	MCF-7	breast:
22	chr7:100859400..100864017-chr7:100886115..100890578,15	K562	blood:
23	chr7:100860435..100861815-chr7:100887125..100888440,6	K562	blood:
24	chr7:100807333..100809689-chr7:100860017..100862230,2	K562	blood:
25	chr7:100850699..100858131-chr7:100858977..100863722,10	K562	blood:

Variant related genes	Relation type
PLOD3	TF binding region
ZNHIT1	TF binding region
ZNHIT1	CpG island
PLOD3	CpG island
ENSG00000106400	Chromatin interaction
ENSG00000205267	Chromatin interaction
ENSG00000169871	Chromatin interaction
ENSG00000106404	Chromatin interaction
ENSG00000214253	Chromatin interaction
ENSG00000128564	Chromatin interaction
ENSG00000232445	Chromatin interaction
ENSG00000106397	Chromatin interaction
ENSG00000087085	Chromatin interaction
ENSG00000176125	Chromatin interaction
ENSG00000106384	Chromatin interaction
ENSG00000213394	Chromatin interaction
ENSG00000167011	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10250685	0.91[ASN][1000 genomes]
rs1047319	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10953330	0.87[ASN][1000 genomes]
rs11769624	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17319250	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2072168	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2302428	0.91[ASN][1000 genomes]
rs28361887	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35082269	0.95[ASN][1000 genomes]
rs35550811	0.82[ASN][1000 genomes]
rs3757459	0.91[ASN][1000 genomes]
rs3757460	0.91[ASN][1000 genomes]
rs4729672	0.93[ASN][1000 genomes]
rs62482972	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831075	chr7:100692297-100917018	Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv1030604	chr7:100717732-101223465	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	esv2422376	chr7:100743485-101016471	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
5	nsv1018841	chr7:100760410-100868299	Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	nsv534186	chr7:100773842-100898909	Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv607973	chr7:100782460-100873835	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
8	nsv888816	chr7:100792810-100862264	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv464651	chr7:100792810-100971604	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
10	nsv607974	chr7:100792810-100971604	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
11	nsv429788	chr7:100799565-101178565	Weak transcription Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
12	esv2752134	chr7:100800131-101141867	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
13	nsv607975	chr7:100804140-100873835	Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
14	nsv464652	chr7:100804140-100881640	Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv607976	chr7:100804140-100881640	Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv888817	chr7:100804140-100881640	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
17	nsv607977	chr7:100818846-100881640	Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
18	nsv831076	chr7:100828847-101011674	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
19	nsv888818	chr7:100833153-100895480	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
20	nsv888819	chr7:100833153-100920007	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
21	esv2422326	chr7:100833449-101000131	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100859200-100862200	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr7:100859400-100862600	Active TSS	HSMM	muscle
3	chr7:100859600-100860800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:100859600-100862000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:100859600-100862400	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr7:100859600-100862400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:100859600-100862400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr7:100859600-100862600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:100859800-100860800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
10	chr7:100859800-100861000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:100859800-100861200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
12	chr7:100859800-100861200	Flanking Active TSS	Primary hematopoietic stem cells	blood
13	chr7:100859800-100861200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr7:100859800-100862000	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr7:100859800-100862000	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr7:100859800-100862000	Active TSS	Right Atrium	heart
17	chr7:100859800-100862200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:100859800-100862200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:100859800-100862400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:100859800-100862400	Active TSS	H9 Cell Line	embryonic stem cell
21	chr7:100859800-100862600	Active TSS	HSMMtube	muscle
22	chr7:100860000-100860800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr7:100860000-100860800	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr7:100860000-100861800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr7:100860000-100862000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr7:100860000-100862000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr7:100860000-100862000	Active TSS	A549	lung
28	chr7:100860000-100862000	Active TSS	Hela-S3	cervix
29	chr7:100860000-100862000	Active TSS	Osteobl	bone
30	chr7:100860000-100862200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr7:100860000-100862200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:100860000-100862200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr7:100860000-100862200	Active TSS	Fetal Kidney	kidney
34	chr7:100860000-100862200	Active TSS	GM12878-XiMat	blood
35	chr7:100860000-100862200	Active TSS	HMEC	breast
36	chr7:100860000-100862200	Active TSS	NHDF-Ad	bronchial
37	chr7:100860000-100862400	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr7:100860000-100862400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:100860000-100862400	Active TSS	Aorta	Aorta
40	chr7:100860000-100862400	Bivalent/Poised TSS	HepG2	liver
41	chr7:100860000-100862400	Active TSS	NHLF	lung
42	chr7:100860000-100862600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr7:100860200-100861600	Active TSS	Colon Smooth Muscle	Colon
44	chr7:100860200-100861800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:100860200-100861800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
46	chr7:100860200-100861800	Active TSS	Brain Hippocampus Middle	brain
47	chr7:100860200-100861800	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr7:100860200-100861800	Active TSS	Brain Substantia Nigra	brain
49	chr7:100860200-100861800	Active TSS	Fetal Brain Female	brain
50	chr7:100860200-100861800	Active TSS	Fetal Lung	lung

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