Variant report

Variant	rs17881696
Chromosome Location	chr7:100493359-100493360
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	POLR2A	chr7:100493215-100493986	K562	blood:	n/a	n/a
2	JUN	chr7:100493191-100496118	K562	blood:	n/a	chr7:100494328-100494341 chr7:100493521-100493530
3	POLR2A	chr7:100493320-100493552	K562	blood:	n/a	n/a
4	CTCF	chr7:100491721-100493493	SK-N-SH	brain:	n/a	chr7:100492576-100492594 chr7:100492984-100492997 chr7:100493289-100493302 chr7:100492813-100492822 chr7:100492579-100492592
5	SIN3A	chr7:100493338-100493446	H1-hESC	embryonic stem cell:	n/a	n/a
6	ZBTB7A	chr7:100492302-100493511	K562	blood:	n/a	n/a
7	EGR1	chr7:100493043-100493502	ECC-1	luminal epithelium:	n/a	chr7:100493231-100493244 chr7:100493232-100493243 chr7:100493233-100493243 chr7:100493231-100493244 chr7:100493231-100493245 chr7:100493233-100493243 chr7:100493227-100493249 chr7:100493231-100493244 chr7:100493234-100493243 chr7:100493232-100493243 chr7:100493233-100493242 chr7:100493256-100493266
8	HMGN3	chr7:100492415-100495041	K562	blood:	n/a	n/a
9	ZBTB7A	chr7:100492182-100495231	K562	blood:	n/a	n/a
10	PAX5	chr7:100493182-100493484	GM12892	blood:	n/a	n/a
11	MAX	chr7:100492833-100493531	K562	blood:	n/a	n/a
12	ELF1	chr7:100492338-100493495	GM12878	blood:	n/a	chr7:100493197-100493209 chr7:100492571-100492580 chr7:100493216-100493228 chr7:100492574-100492583 chr7:100492740-100492752 chr7:100493292-100493304
13	UBTF	chr7:100492437-100494200	K562	blood:	n/a	n/a
14	EGR1	chr7:100493055-100494141	MCF-7	breast:	n/a	chr7:100493231-100493244 chr7:100493232-100493243 chr7:100493233-100493243 chr7:100493231-100493244 chr7:100493231-100493245 chr7:100493233-100493243 chr7:100493508-100493522 chr7:100493531-100493545 chr7:100493227-100493249 chr7:100493231-100493244 chr7:100493234-100493243 chr7:100493581-100493595 chr7:100493232-100493243 chr7:100493562-100493576 chr7:100493233-100493242 chr7:100493256-100493266 chr7:100493512-100493522
15	SIN3AK20	chr7:100493295-100493910	K562	blood:	n/a	n/a
16	SIN3AK20	chr7:100493077-100494075	PANC-1	pancreas:	n/a	n/a
17	HDAC2	chr7:100492345-100495320	MCF-7	breast:	n/a	n/a
18	EGR1	chr7:100492691-100494069	K562	blood:	n/a	chr7:100493231-100493244 chr7:100493232-100493243 chr7:100493233-100493243 chr7:100493231-100493244 chr7:100493231-100493245 chr7:100492856-100492869 chr7:100493233-100493243 chr7:100493508-100493522 chr7:100493531-100493545 chr7:100493227-100493249 chr7:100492860-100492870 chr7:100493231-100493244 chr7:100492743-100492756 chr7:100493234-100493243 chr7:100493581-100493595 chr7:100493232-100493243 chr7:100493562-100493576 chr7:100493233-100493242 chr7:100493256-100493266 chr7:100493512-100493522
19	UBTF	chr7:100492487-100493492	K562	blood:	n/a	n/a
20	CCNT2	chr7:100492094-100495029	K562	blood:	n/a	chr7:100492742-100492751
21	YY1	chr7:100493063-100493511	K562	blood:	n/a	chr7:100493292-100493306 chr7:100493202-100493211 chr7:100493286-100493297 chr7:100493298-100493307 chr7:100493197-100493211
22	MAZ	chr7:100492395-100493417	IMR90	lung:	n/a	n/a
23	E2F6	chr7:100493087-100493504	K562	blood:	n/a	chr7:100493298-100493307
24	ZBTB7A	chr7:100492304-100494646	ECC-1	luminal epithelium:	n/a	n/a
25	EGR1	chr7:100492863-100493940	HCT-116	colon:	n/a	chr7:100493231-100493244 chr7:100493232-100493243 chr7:100493233-100493243 chr7:100493231-100493244 chr7:100493231-100493245 chr7:100493233-100493243 chr7:100493508-100493522 chr7:100493531-100493545 chr7:100493227-100493249 chr7:100493231-100493244 chr7:100493234-100493243 chr7:100493581-100493595 chr7:100493232-100493243 chr7:100493562-100493576 chr7:100493233-100493242 chr7:100493256-100493266 chr7:100493512-100493522
26	POLR2A	chr7:100493214-100493432	PBDE	blood:	n/a	n/a
27	POLR2A	chr7:100493215-100495902	K562	blood:	n/a	n/a
28	POLR2A	chr7:100493043-100493561	H1-neurons	neurons:	n/a	n/a
29	EGR1	chr7:100492404-100493976	K562	blood:	n/a	chr7:100493231-100493244 chr7:100493232-100493243 chr7:100493233-100493243 chr7:100493231-100493244 chr7:100493231-100493245 chr7:100492856-100492869 chr7:100493233-100493243 chr7:100493508-100493522 chr7:100493531-100493545 chr7:100493227-100493249 chr7:100492860-100492870 chr7:100493231-100493244 chr7:100492743-100492756 chr7:100493234-100493243 chr7:100493581-100493595 chr7:100493232-100493243 chr7:100493562-100493576 chr7:100493233-100493242 chr7:100493256-100493266 chr7:100493512-100493522
30	ZBTB7A	chr7:100492311-100494721	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:100491420..100497264-chr7:100607951..100612175,9	K562	blood:
2	chr7:100491799..100497264-chr7:100607837..100612175,9	K562	blood:
3	chr7:100492615..100493493-chr7:100609306..100609962,2	MCF-7	breast:
4	chr7:100270007..100272523-chr7:100492882..100494851,2	K562	blood:
5	chr7:100492344..100495062-chr7:100726871..100729209,3	MCF-7	breast:
6	chr7:100491373..100494455-chr7:100609680..100612292,3	MCF-7	breast:
7	chr7:100491924..100495059-chr7:100886100..100889819,5	MCF-7	breast:
8	chr7:100492733..100496183-chr7:100699112..100703676,5	MCF-7	breast:
9	chr7:100491458..100494589-chr7:100859109..100862606,4	MCF-7	breast:

Variant related genes	Relation type
ACHE	TF binding region
ENSG00000222636	Chromatin interaction
ENSG00000225946	Chromatin interaction
ENSG00000172354	Chromatin interaction
ENSG00000214253	Chromatin interaction
ENSG00000106400	Chromatin interaction
ENSG00000106397	Chromatin interaction
ENSG00000169894	Chromatin interaction
ENSG00000169871	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12666989	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12667888	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12705089	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12705090	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12705091	0.94[EUR][1000 genomes]
rs12705092	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12705095	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12705096	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13226502	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13226864	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13244629	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13245899	0.92[EUR][1000 genomes]
rs17883557	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17884589	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs314370	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs314373	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3757868	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6706	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv464647	chr7:100374087-100497131	Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS 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	90 gene(s)	inside rSNPs	diseases
7	nsv607965	chr7:100374087-100497131	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv1032673	chr7:100382250-100606794	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
9	nsv888799	chr7:100406144-100497131	Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS 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 miRNA target site	89 gene(s)	inside rSNPs	diseases
10	nsv888801	chr7:100416250-100497131	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
11	nsv464648	chr7:100422156-100518458	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
12	nsv607966	chr7:100422156-100518458	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS 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 miRNA target site	90 gene(s)	inside rSNPs	diseases
13	nsv831073	chr7:100425659-100544888	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
14	nsv888802	chr7:100484917-100495530	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
15	nsv888803	chr7:100486656-100497131	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
16	nsv888804	chr7:100486754-100494202	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
17	nsv888805	chr7:100486754-100498057	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
18	nsv482110	chr7:100487616-100493541	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	36 gene(s)	inside rSNPs	diseases
19	nsv888806	chr7:100488407-100495530	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
20	nsv888807	chr7:100490077-100498057	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv888808	chr7:100490981-100498057	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
22	nsv888809	chr7:100491451-100495530	Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
23	nsv888810	chr7:100492127-100495530	Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv888811	chr7:100492127-100497131	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
25	nsv888812	chr7:100492127-100498057	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
26	nsv888813	chr7:100492322-100495530	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
27	nsv607969	chr7:100492357-100493998	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
28	nsv888814	chr7:100492357-100495530	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
29	nsv888815	chr7:100492357-100497131	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
30	nsv607970	chr7:100492493-100494949	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs17881696	ACHE	cis	Artery Tibial	GTEx
rs17881696	ACHE	cis	Nerve Tibial	GTEx
rs17881696	ACHE	cis	Artery Aorta	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100491200-100493600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:100491600-100493400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:100491800-100493600	Active TSS	H9 Cell Line	embryonic stem cell
4	chr7:100491800-100493600	Active TSS	HSMM	muscle
5	chr7:100491800-100493800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
6	chr7:100491800-100495000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
7	chr7:100492000-100493400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr7:100492000-100493600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:100492000-100493600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:100492000-100493600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:100492000-100493800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
12	chr7:100492000-100493800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:100492000-100494000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:100492200-100493400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:100492200-100493400	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
16	chr7:100492200-100493600	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr7:100492200-100493600	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr7:100492200-100493600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
19	chr7:100492200-100493600	Active TSS	Skeletal Muscle Female	skeletal muscle
20	chr7:100492200-100493800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
21	chr7:100492200-100493800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
22	chr7:100492200-100493800	Active TSS	HepG2	liver
23	chr7:100492200-100494200	Bivalent Enhancer	Spleen	Spleen
24	chr7:100492200-100495000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr7:100492400-100493400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
26	chr7:100492400-100493400	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
27	chr7:100492400-100493400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
28	chr7:100492400-100493400	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr7:100492400-100493400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:100492400-100493600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
31	chr7:100492400-100493600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
32	chr7:100492400-100493600	Bivalent Enhancer	Fetal Brain Male	brain
33	chr7:100492400-100493600	Active TSS	A549	lung
34	chr7:100492400-100493800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:100492400-100493800	Active TSS	Rectal Smooth Muscle	rectum
36	chr7:100492400-100493800	Bivalent/Poised TSS	Thymus	Thymus
37	chr7:100492400-100494000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr7:100492400-100494200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
39	chr7:100492400-100494400	Active TSS	Psoas Muscle	Psoas
40	chr7:100492600-100493400	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:100492600-100493400	Flanking Active TSS	Primary B cells from cord blood	blood
42	chr7:100492600-100493400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr7:100492600-100493400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr7:100492600-100493400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
45	chr7:100492600-100493400	Active TSS	Aorta	Aorta
46	chr7:100492600-100493400	Flanking Bivalent TSS/Enh	HMEC	breast
47	chr7:100492600-100493400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
48	chr7:100492600-100493600	Active TSS	Right Atrium	heart
49	chr7:100492600-100493600	Active TSS	Right Ventricle	heart
50	chr7:100492600-100493600	Active TSS	K562	blood

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