Variant report

Variant	rs17883552
Chromosome Location	chr7:100492357-100492358
allele	A/C
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	REST	chr7:100492332-100492633	A549	lung:	n/a	n/a
2	CTCF	chr7:100492350-100492844	MCF-7	breast:	n/a	chr7:100492576-100492594 chr7:100492813-100492822 chr7:100492579-100492592
3	RAD21	chr7:100492293-100492869	H1-hESC	embryonic stem cell:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
4	POLR2A	chr7:100491682-100492423	PBDE	blood:	n/a	n/a
5	RAD21	chr7:100492240-100492985	H1-hESC	embryonic stem cell:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
6	RAD21	chr7:100492293-100493033	MCF-7	breast:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
7	SMC3	chr7:100491838-100492873	GM12878	blood:	n/a	chr7:100492630-100492640
8	RAD21	chr7:100492354-100492819	A549	lung:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
9	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
10	JUN	chr7:100492328-100492858	K562	blood:	n/a	n/a
11	CTCF	chr7:100492010-100492794	K562	blood:	n/a	chr7:100492576-100492594 chr7:100492579-100492592
12	ZBTB7A	chr7:100492302-100493511	K562	blood:	n/a	n/a
13	SIN3AK20	chr7:100492314-100492993	PANC-1	pancreas:	n/a	n/a
14	ZBTB7A	chr7:100492182-100495231	K562	blood:	n/a	n/a
15	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
16	CTCF	chr7:100492233-100492367	GM19239	blood:	n/a	n/a
17	MAX	chr7:100492322-100492811	H1-hESC	embryonic stem cell:	n/a	n/a
18	GATA1	chr7:100491612-100492603	PBDE	blood:	n/a	n/a
19	RAD21	chr7:100492253-100493054	HCT-116	colon:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
20	RAD21	chr7:100492316-100492946	MCF-7	breast:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
21	YY1	chr7:100492351-100492773	HepG2	liver:	n/a	chr7:100492571-100492580 chr7:100492743-100492754 chr7:100492575-100492589 chr7:100492745-100492754 chr7:100492489-100492500
22	ELF1	chr7:100492356-100492919	K562	blood:	n/a	chr7:100492571-100492580 chr7:100492574-100492583 chr7:100492740-100492752
23	MAX	chr7:100492322-100492786	K562	blood:	n/a	n/a
24	CTCF	chr7:100492305-100492855	HCT-116	colon:	n/a	chr7:100492576-100492594 chr7:100492813-100492822 chr7:100492579-100492592
25	HDAC2	chr7:100492345-100495320	MCF-7	breast:	n/a	n/a
26	RAD21	chr7:100492286-100492898	ECC-1	luminal epithelium:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
27	NR2F2	chr7:100492343-100492817	K562	blood:	n/a	n/a
28	RAD21	chr7:100492301-100493066	HCT-116	colon:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
29	CCNT2	chr7:100492094-100495029	K562	blood:	n/a	chr7:100492742-100492751
30	CTCF	chr7:100492029-100493295	A549	lung:	n/a	chr7:100492576-100492594 chr7:100492984-100492997 chr7:100492813-100492822 chr7:100492579-100492592
31	SMC3	chr7:100492006-100492820	Hela-S3	cervix:	n/a	chr7:100492630-100492640
32	CTCF	chr7:100492011-100492833	GM12878	blood:	n/a	chr7:100492576-100492594 chr7:100492813-100492822 chr7:100492579-100492592
33	CTCF	chr7:100492242-100493120	HCT-116	colon:	n/a	chr7:100492576-100492594 chr7:100492984-100492997 chr7:100492813-100492822 chr7:100492579-100492592
34	CTCF	chr7:100492251-100493162	K562	blood:	n/a	chr7:100492576-100492594 chr7:100492984-100492997 chr7:100492813-100492822 chr7:100492579-100492592
35	CTCF	chr7:100492310-100492881	K562	blood:	n/a	chr7:100492576-100492594 chr7:100492813-100492822 chr7:100492579-100492592
36	ZBTB7A	chr7:100492304-100494646	ECC-1	luminal epithelium:	n/a	n/a
37	SMC3	chr7:100492010-100492789	K562	blood:	n/a	chr7:100492630-100492640
38	STAT1	chr7:100491959-100492418	Hela-S3	cervix:	n/a	chr7:100492158-100492169 chr7:100492160-100492169 chr7:100492154-100492174 chr7:100492389-100492397 chr7:100492154-100492174 chr7:100492160-100492168 chr7:100492159-100492168
39	CTCF	chr7:100492268-100492998	MCF-7	breast:	n/a	chr7:100492576-100492594 chr7:100492984-100492997 chr7:100492813-100492822 chr7:100492579-100492592
40	RAD21	chr7:100492299-100492940	A549	lung:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
41	CTCF	chr7:100492280-100492362	Spleen_OC	spleen:	n/a	n/a
42	RAD21	chr7:100492344-100492860	HepG2	liver:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
43	CTCF	chr7:100492334-100492810	H1-hESC	embryonic stem cell:	n/a	chr7:100492576-100492594 chr7:100492579-100492592
44	CTCF	chr7:100492349-100492813	A549	lung:	n/a	chr7:100492576-100492594 chr7:100492579-100492592
45	RAD21	chr7:100491873-100493134	SK-N-SH	brain:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
46	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	chr7:100492296..100493068-chr7:100887259..100887881,3	MCF-7	breast:
3	chr7:100491227..100493354-chr7:100886184..100889152,2	K562	blood:
4	chr7:100491799..100497264-chr7:100607837..100612175,9	K562	blood:
5	chr7:100492151..100493007-chr7:100781451..100782108,2	MCF-7	breast:
6	chr7:100492126..100493072-chr7:100720609..100721480,6	MCF-7	breast:
7	chr7:100490569..100492448-chr7:100550621..100553306,2	MCF-7	breast:
8	chr7:100492344..100495062-chr7:100726871..100729209,3	MCF-7	breast:
9	chr7:100492173..100493049-chr7:100701899..100703390,5	K562	blood:
10	chr7:100491373..100494455-chr7:100609680..100612292,3	MCF-7	breast:
11	chr7:100491924..100495059-chr7:100886100..100889819,5	MCF-7	breast:
12	chr7:100491458..100494589-chr7:100859109..100862606,4	MCF-7	breast:

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

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17162500	1.00[MEX][hapmap];0.82[YRI][hapmap]
rs17162522	0.81[LWK][hapmap];1.00[MEX][hapmap];0.86[YRI][hapmap]
rs17880400	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56970616	0.87[AMR][1000 genomes]
rs57066808	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs57981438	0.87[AMR][1000 genomes]
rs58170575	1.00[AMR][1000 genomes]
rs58629441	0.87[AMR][1000 genomes]
rs61700243	0.87[AMR][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	nsv607968	chr7:100486035-100492896	Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	39 gene(s)	inside rSNPs	diseases
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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

No data

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100488200-100492600	Weak transcription	Liver	Liver
2	chr7:100488800-100492400	Weak transcription	Lung	lung
3	chr7:100488800-100492400	Weak transcription	Right Atrium	heart
4	chr7:100488800-100492600	Weak transcription	Aorta	Aorta
5	chr7:100488800-100492800	Weak transcription	Small Intestine	intestine
6	chr7:100489000-100492400	Weak transcription	Left Ventricle	heart
7	chr7:100489000-100492400	Weak transcription	Pancreas	Pancrea
8	chr7:100489000-100492400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:100489000-100492600	Weak transcription	Ovary	ovary
10	chr7:100489200-100492400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr7:100489200-100492800	Weak transcription	Brain Substantia Nigra	brain
12	chr7:100490000-100492400	Weak transcription	NH-A	brain
13	chr7:100491200-100493600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:100491400-100492400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:100491400-100492600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:100491600-100492400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:100491600-100493400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr7:100491800-100492400	Bivalent Enhancer	Brain Germinal Matrix	brain
19	chr7:100491800-100492400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
20	chr7:100491800-100492400	Enhancers	Fetal Lung	lung
21	chr7:100491800-100492600	Flanking Active TSS	Fetal Muscle Leg	muscle
22	chr7:100491800-100492600	Bivalent/Poised TSS	Fetal Thymus	thymus
23	chr7:100491800-100493600	Active TSS	H9 Cell Line	embryonic stem cell
24	chr7:100491800-100493600	Active TSS	HSMM	muscle
25	chr7:100491800-100493800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
26	chr7:100491800-100495000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
27	chr7:100492000-100492400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
28	chr7:100492000-100492400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:100492000-100492400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
30	chr7:100492000-100492400	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
31	chr7:100492000-100492400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr7:100492000-100492400	Enhancers	Right Ventricle	heart
33	chr7:100492000-100492400	Enhancers	A549	lung
34	chr7:100492000-100492600	Enhancers	Placenta	Placenta
35	chr7:100492000-100492600	Flanking Active TSS	HSMMtube	muscle
36	chr7:100492000-100492800	Active TSS	Hela-S3	cervix
37	chr7:100492000-100493200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr7:100492000-100493400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:100492000-100493600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr7:100492000-100493600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:100492000-100493600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:100492000-100493800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
43	chr7:100492000-100493800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr7:100492000-100494000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:100492200-100492400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:100492200-100492400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:100492200-100492400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
48	chr7:100492200-100492400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr7:100492200-100492400	Enhancers	Muscle Satellite Cultured Cells	--
50	chr7:100492200-100492400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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