Variant report

Variant	rs28361887
Chromosome Location	chr7:100860401-100860402
allele	C/T
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	CTCF	chr7:100860380-100860530	GM12865	blood:	n/a	n/a
2	ELF1	chr7:100860065-100861977	MCF-7	breast:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
3	CTCF	chr7:100860390-100860535	GM20000	blood:	n/a	n/a
4	CTCF	chr7:100860340-100860490	BE2_C	brain:	n/a	n/a
5	MYC	chr7:100860271-100860416	MCF-7	breast:	n/a	chr7:100860333-100860343
6	ZBTB7A	chr7:100860137-100861098	ECC-1	luminal epithelium:	n/a	chr7:100860641-100860650
7	MAX	chr7:100860060-100861813	Hela-S3	cervix:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
8	POLR2A	chr7:100860373-100861648	Gliobla	brain:	n/a	n/a
9	MXI1	chr7:100859501-100862549	IMR90	lung:	n/a	chr7:100861332-100861347
10	SIN3AK20	chr7:100859882-100862120	MCF-7	breast:	n/a	n/a
11	POLR2A	chr7:100859817-100863220	HepG2	liver:	n/a	n/a
12	ELF1	chr7:100860292-100861898	GM12878	blood:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
13	ETS1	chr7:100860254-100861192	K562	blood:	n/a	chr7:100860406-100860417
14	CBX3	chr7:100859882-100862021	K562	blood:	n/a	n/a
15	UBTF	chr7:100860104-100861180	K562	blood:	n/a	n/a
16	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
17	POLR2A	chr7:100860009-100861708	MCF-7	breast:	n/a	n/a
18	MAX	chr7:100859842-100861976	K562	blood:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
19	JUND	chr7:100860399-100861061	A549	lung:	n/a	chr7:100860559-100860568
20	TAF1	chr7:100860336-100861925	ECC-1	luminal epithelium:	n/a	n/a
21	TCF12	chr7:100860255-100861637	ECC-1	luminal epithelium:	n/a	n/a
22	POLR2A	chr7:100860229-100861738	H1-neurons	neurons:	n/a	n/a
23	ELF1	chr7:100860394-100861913	MCF-7	breast:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
24	E2F6	chr7:100859974-100861069	K562	blood:	n/a	chr7:100860148-100860159 chr7:100860306-100860321 chr7:100860334-100860349 chr7:100860132-100860143 chr7:100860304-100860314
25	MTA3	chr7:100860348-100861861	GM12878	blood:	n/a	n/a
26	SIN3AK20	chr7:100860157-100861906	MCF-7	breast:	n/a	n/a
27	POLR2A	chr7:100860154-100861814	SK-N-MC	brain:	n/a	n/a
28	NR2F2	chr7:100860212-100861442	MCF-7	breast:	n/a	n/a
29	CTCFL	chr7:100860373-100860753	K562	blood:	n/a	n/a
30	SIN3AK20	chr7:100860336-100861667	PANC-1	pancreas:	n/a	n/a
31	POLR2A	chr7:100860338-100861697	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr7:100860400-100860550	AG04450	lung:	n/a	n/a
33	E2F6	chr7:100859824-100861128	A549	lung:	n/a	chr7:100860148-100860159 chr7:100860306-100860321 chr7:100860334-100860349 chr7:100860132-100860143 chr7:100860304-100860314
34	MAX	chr7:100859752-100860566	H1-hESC	embryonic stem cell:	n/a	chr7:100860333-100860343
35	POLR2A	chr7:100859728-100861722	PFSK-1	brain:	n/a	n/a
36	ELF1	chr7:100860369-100861697	K562	blood:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
37	MAX	chr7:100859833-100862032	MCF-7	breast:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
38	PML	chr7:100860394-100861673	K562	blood:	n/a	chr7:100861354-100861363
39	ZBTB7A	chr7:100860055-100861188	ECC-1	luminal epithelium:	n/a	chr7:100860641-100860650
40	E2F6	chr7:100859542-100861080	H1-hESC	embryonic stem cell:	n/a	chr7:100860148-100860159 chr7:100860306-100860321 chr7:100860334-100860349 chr7:100860132-100860143 chr7:100860304-100860314
41	POLR2A	chr7:100860184-100861854	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr7:100860400-100860550	HVMF	connective:	n/a	n/a
43	MXI1	chr7:100860207-100861887	HepG2	liver:	n/a	chr7:100861332-100861347
44	POLR2A	chr7:100860227-100861628	A549	lung:	n/a	n/a
45	CTCF	chr7:100860400-100860550	GM12875	blood:	n/a	n/a
46	GABPA	chr7:100860198-100862232	MCF-7	breast:	n/a	chr7:100861371-100861385 chr7:100861432-100861446 chr7:100861371-100861382 chr7:100861435-100861446 chr7:100861437-100861446
47	POLR2A	chr7:100860340-100861804	U87	brain:	n/a	n/a
48	EGR1	chr7:100860369-100861748	HCT-116	colon:	n/a	chr7:100861288-100861297 chr7:100861517-100861530 chr7:100861372-100861381 chr7:100861436-100861445 chr7:100861395-100861404
49	YY1	chr7:100860130-100861937	SK-N-SH	brain:	n/a	chr7:100861301-100861323 chr7:100861312-100861321
50	POLR2A	chr7:100859625-100861925	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100860399-100860449	HMEC	breast:	n/a
2	chr7:100860399-100860449	HL-60	blood:	n/a
3	chr7:100860399-100860449	AG10803	skin:	n/a
4	chr7:100860399-100860449	A549	lung:	n/a
5	chr7:100860399-100860449	SKMC	muscle:	n/a
6	chr7:100860399-100860449	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:100860399-100860449	NB4	blood:	n/a
8	chr7:100860399-100860449	Hela-S3	cervix:	n/a
9	chr7:100860399-100860449	AG04449	skin:	fetal
10	chr7:100860399-100860449	GM19239	blood:	n/a
11	chr7:100860399-100860449	Jurkat	blood:	n/a
12	chr7:100860399-100860449	NHBE	bronchial:	n/a
13	chr7:100860399-100860449	K562	blood:	n/a
14	chr7:100860399-100860449	GM12878	blood:	n/a
15	chr7:100860399-100860449	HRE	kidney:	n/a
16	chr7:100860399-100860449	PFSK-1	brain:	n/a
17	chr7:100860399-100860449	GM12891	blood:	n/a
18	chr7:100860399-100860449	HCF	heart:	n/a
19	chr7:100860399-100860449	GM06990	blood:	n/a
20	chr7:100860399-100860449	HRPEpiC	eye:	n/a
21	chr7:100860399-100860449	HEK293	kidney:	embryo
22	chr7:100860399-100860449	AG04450	lung:	fetal
23	chr7:100860399-100860449	HRCEpiC	kidney:	n/a
24	chr7:100860399-100860449	LNCaP	prostate:	n/a
25	chr7:100860399-100860449	PANC-1	pancreas:	n/a
26	chr7:100860399-100860449	ProgFib	skin:	n/a
27	chr7:100860399-100860449	HEEpiC	esophagus:	n/a
28	chr7:100860399-100860449	BJ	skin:	n/a
29	chr7:100860399-100860449	AoSMC	blood vessel:	n/a
30	chr7:100860399-100860449	BE2_C	brain:	n/a
31	chr7:100860399-100860449	MCF-7	breast:	n/a
32	chr7:100860399-100860449	IMR90	lung:	fetal
33	chr7:100860399-100860449	SK-N-SH_RA	brain:	n/a
34	chr7:100860399-100860449	T-47D	breast:	n/a
35	chr7:100860399-100860449	H1-hESC	embryonic stem cell:	embryo
36	chr7:100860399-100860449	AG09309	skin:	n/a
37	chr7:100860399-100860449	ovcar-3	ovarian:	n/a
38	chr7:100860399-100860449	GM12892	blood:	n/a
39	chr7:100860399-100860449	NT2-D1	testis:	n/a
40	chr7:100860399-100860449	SK-N-SH	brain:	n/a
41	chr7:100860399-100860449	U87	brain:	n/a
42	chr7:100860399-100860449	HIPEpiC	eye:	n/a
43	chr7:100860399-100860449	HNPCEpiC	eye:	n/a
44	chr7:100860399-100860449	RPTEC	kidney:	n/a
45	chr7:100860399-100860449	NH-A	brain:	n/a
46	chr7:100860399-100860449	Hepatocyte	liver:	n/a
47	chr7:100860399-100860449	CMK	blood:	n/a
48	chr7:100860399-100860449	MCF10A-Er-Src	breast:	n/a
49	chr7:100860399-100860449	HCM	heart:	n/a
50	chr7:100860399-100860449	HUVEC	blood vessel:	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	chr7:100859409..100862433-chr7:100893851..100895703,4	K562	blood:
13	chr7:100858977..100861910-chr7:100881462..100883229,2	K562	blood:
14	chr7:100486477..100489401-chr7:100859928..100862607,2	MCF-7	breast:
15	chr7:100843889..100849523-chr7:100857776..100861352,9	MCF-7	breast:
16	chr7:100491458..100494589-chr7:100859109..100862606,4	MCF-7	breast:
17	chr7:100859877..100865511-chr7:100878168..100882490,7	MCF-7	breast:
18	chr7:100853413..100857189-chr7:100859048..100862216,5	K562	blood:
19	chr7:100858478..100862757-chr7:100884994..100890276,15	MCF-7	breast:
20	chr7:100853184..100857478-chr7:100859517..100863375,8	MCF-7	breast:
21	chr7:100859400..100864017-chr7:100886115..100890578,15	K562	blood:
22	chr7:100807333..100809689-chr7:100860017..100862230,2	K562	blood:
23	chr7:100850699..100858131-chr7:100858977..100863722,10	K562	blood:

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

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10250685	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1047319	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1056678	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10953329	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10953330	0.87[ASN][1000 genomes]
rs11769624	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17319250	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2072168	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2074685	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2302428	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs35082269	0.95[ASN][1000 genomes]
rs35094522	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs35550811	0.82[ASN][1000 genomes]
rs3757459	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3757460	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4729672	0.84[AMR][1000 genomes];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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs28361887	ZNHIT1	cis	Esophagus Mucosa	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100859200-100860600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr7:100859200-100862200	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr7:100859400-100860600	Flanking Active TSS	Colonic Mucosa	Colon
4	chr7:100859400-100862600	Active TSS	HSMM	muscle
5	chr7:100859600-100860600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
6	chr7:100859600-100860600	Flanking Active TSS	Adipose Nuclei	Adipose
7	chr7:100859600-100860600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr7:100859600-100860600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr7:100859600-100860600	Flanking Active TSS	Dnd41	blood
10	chr7:100859600-100860800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:100859600-100862000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr7:100859600-100862400	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr7:100859600-100862400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:100859600-100862400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:100859600-100862600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:100859800-100860600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:100859800-100860600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:100859800-100860600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
19	chr7:100859800-100860800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
20	chr7:100859800-100861000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:100859800-100861200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
22	chr7:100859800-100861200	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr7:100859800-100861200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr7:100859800-100862000	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr7:100859800-100862000	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr7:100859800-100862000	Active TSS	Right Atrium	heart
27	chr7:100859800-100862200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:100859800-100862200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:100859800-100862400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr7:100859800-100862400	Active TSS	H9 Cell Line	embryonic stem cell
31	chr7:100859800-100862600	Active TSS	HSMMtube	muscle
32	chr7:100860000-100860600	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr7:100860000-100860600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
34	chr7:100860000-100860600	Flanking Active TSS	Spleen	Spleen
35	chr7:100860000-100860800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr7:100860000-100860800	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr7:100860000-100861800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:100860000-100862000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr7:100860000-100862000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr7:100860000-100862000	Active TSS	A549	lung
41	chr7:100860000-100862000	Active TSS	Hela-S3	cervix
42	chr7:100860000-100862000	Active TSS	Osteobl	bone
43	chr7:100860000-100862200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:100860000-100862200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr7:100860000-100862200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:100860000-100862200	Active TSS	Fetal Kidney	kidney
47	chr7:100860000-100862200	Active TSS	GM12878-XiMat	blood
48	chr7:100860000-100862200	Active TSS	HMEC	breast
49	chr7:100860000-100862200	Active TSS	NHDF-Ad	bronchial
50	chr7:100860000-100862400	Active TSS	iPS-18 Cell Line	embryonic stem cell

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