Variant report

Variant	rs55813648
Chromosome Location	chr1:92355683-92355684
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	FOXA1	chr1:92355599-92355928	HepG2	liver:	n/a	n/a
2	RAD21	chr1:92355570-92355990	Hela-S3	cervix:	n/a	chr1:92355702-92355712
3	FOS	chr1:92355466-92356007	MCF10A-Er-Src	breast:	n/a	chr1:92355829-92355840 chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
4	MXI1	chr1:92355396-92355981	Hela-S3	cervix:	n/a	n/a
5	SMC3	chr1:92355527-92355956	Hela-S3	cervix:	n/a	n/a
6	FOXA1	chr1:92355622-92355993	HepG2	liver:	n/a	n/a
7	MAX	chr1:92355394-92355980	Hela-S3	cervix:	n/a	n/a
8	FOXA1	chr1:92355622-92355931	HepG2	liver:	n/a	n/a
9	CTCF	chr1:92355560-92355710	HMF	breast:	n/a	n/a
10	SP1	chr1:92355290-92355989	A549	lung:	n/a	n/a
11	CTCF	chr1:92355680-92355830	HEEpiC	esophagus:	n/a	n/a
12	POLR2A	chr1:92355533-92355783	MCF10A-Er-Src	breast:	n/a	n/a
13	GTF2F1	chr1:92355545-92355920	Hela-S3	cervix:	n/a	n/a
14	FOSL2	chr1:92355625-92355974	A549	lung:	n/a	chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
15	BRCA1	chr1:92355585-92355965	Hela-S3	cervix:	n/a	chr1:92355861-92355868
16	FOS	chr1:92355651-92355978	HUVEC	blood vessel:	n/a	chr1:92355829-92355840 chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
17	FOSL2	chr1:92355471-92356086	A549	lung:	n/a	chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
18	SP1	chr1:92355204-92355931	A549	lung:	n/a	n/a
19	CTCF	chr1:92355600-92355750	HEEpiC	esophagus:	n/a	n/a
20	SIN3AK20	chr1:92355582-92355978	MCF-7	breast:	n/a	n/a
21	MYC	chr1:92355437-92355970	MCF10A-Er-Src	breast:	n/a	n/a
22	MAX	chr1:92355351-92355954	Hela-S3	cervix:	n/a	n/a
23	FOS	chr1:92355468-92355967	Hela-S3	cervix:	n/a	chr1:92355829-92355840 chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
24	FOXA2	chr1:92355258-92356044	A549	lung:	n/a	n/a
25	FOXA1	chr1:92355682-92356004	HepG2	liver:	n/a	n/a
26	CTCF	chr1:92355660-92355810	SAEC	small airway:	n/a	n/a
27	CTCF	chr1:92355680-92355830	Hela-S3	cervix:	n/a	n/a
28	STAT3	chr1:92355563-92355960	MCF10A-Er-Src	breast:	n/a	n/a
29	FOSL2	chr1:92355580-92356055	MCF-7	breast:	n/a	chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
30	RCOR1	chr1:92355549-92355961	Hela-S3	cervix:	n/a	n/a
31	MYC	chr1:92355642-92355985	MCF10A-Er-Src	breast:	n/a	n/a
32	TCF7L2	chr1:92355373-92356056	Hela-S3	cervix:	n/a	n/a
33	JUND	chr1:92355597-92356011	Hela-S3	cervix:	n/a	chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
34	CTCF	chr1:92355560-92355710	HMEC	breast:	n/a	n/a
35	CTCF	chr1:92355660-92355810	AG10803	skin:	n/a	n/a
36	TCF12	chr1:92355231-92356133	A549	lung:	n/a	n/a
37	JUN	chr1:92355564-92355988	Hela-S3	cervix:	n/a	chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
38	EP300	chr1:92355510-92355984	Hela-S3	cervix:	n/a	n/a
39	FOS	chr1:92355651-92356005	MCF10A-Er-Src	breast:	n/a	chr1:92355829-92355840 chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
40	STAT3	chr1:92355573-92355960	Hela-S3	cervix:	n/a	n/a
41	FOXA2	chr1:92355577-92356065	A549	lung:	n/a	n/a
42	MAFK	chr1:92355571-92355956	Hela-S3	cervix:	n/a	n/a
43	GATA3	chr1:92355411-92356309	MCF-7	breast:	n/a	n/a
44	FOS	chr1:92355534-92356022	MCF10A-Er-Src	breast:	n/a	chr1:92355829-92355840 chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
45	FOSL1	chr1:92355522-92356053	HCT-116	colon:	n/a	chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
46	NFIC	chr1:92355480-92356054	ECC-1	luminal epithelium:	n/a	n/a
47	FOSL2	chr1:92355672-92356100	MCF-7	breast:	n/a	chr1:92355830-92355840 chr1:92355830-92355840 chr1:92355831-92355839 chr1:92355830-92355840
48	GATA3	chr1:92355565-92356122	MCF-7	breast:	n/a	n/a
49	EP300	chr1:92355192-92355965	A549	lung:	n/a	n/a
50	NFIC	chr1:92355568-92356029	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:92348748..92351822-chr1:92353645..92358232,4	K562	blood:
2	chr1:92354436..92357349-chr1:92361835..92364580,4	K562	blood:

Variant related genes	Relation type
TGFBR3	TF binding region
ENSG00000069702	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs11466552	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11466555	1.00[ASN][1000 genomes]
rs12032808	1.00[ASN][1000 genomes]
rs17131587	1.00[ASN][1000 genomes]
rs17131594	1.00[ASN][1000 genomes]
rs17886020	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2799519	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2799520	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3862907	1.00[ASN][1000 genomes]
rs4367824	1.00[ASN][1000 genomes]
rs57053265	1.00[ASN][1000 genomes]
rs58094327	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs58281825	1.00[ASN][1000 genomes]
rs59345962	1.00[ASN][1000 genomes]
rs60483196	1.00[ASN][1000 genomes]
rs60765274	1.00[ASN][1000 genomes]
rs61053596	1.00[ASN][1000 genomes]
rs6604065	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6604066	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6656473	1.00[ASN][1000 genomes]
rs6663157	1.00[ASN][1000 genomes]
rs66687439	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6674287	0.83[AMR][1000 genomes]
rs6696315	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6699466	1.00[ASN][1000 genomes]
rs6700124	1.00[ASN][1000 genomes]
rs6703718	1.00[ASN][1000 genomes]
rs67510747	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67577913	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72716472	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72716484	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74101025	1.00[ASN][1000 genomes]
rs74101047	1.00[ASN][1000 genomes]
rs74101048	1.00[ASN][1000 genomes]
rs74101069	1.00[ASN][1000 genomes]
rs74101079	1.00[ASN][1000 genomes]
rs74101080	1.00[ASN][1000 genomes]
rs74101081	1.00[ASN][1000 genomes]
rs74101089	1.00[ASN][1000 genomes]
rs74101097	1.00[ASN][1000 genomes]
rs7514679	1.00[ASN][1000 genomes]
rs7516759	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7516778	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7525713	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7537629	0.82[AMR][1000 genomes]
rs7540938	1.00[ASN][1000 genomes]
rs7541252	1.00[ASN][1000 genomes]
rs7544958	1.00[ASN][1000 genomes]
rs7545710	1.00[ASN][1000 genomes]
rs877277	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs883872	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs883873	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1005917	chr1:92189945-92378683	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv546818	chr1:92236048-92579206	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv546819	chr1:92256626-92558583	Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv546820	chr1:92273644-92558583	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription 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	13 gene(s)	inside rSNPs	diseases
21	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
22	nsv1007270	chr1:92289298-92598800	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
23	nsv1002730	chr1:92302541-92565229	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv830581	chr1:92317207-92511175	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
25	nsv871415	chr1:92340684-92641607	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92352400-92356400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:92352400-92356400	Weak transcription	Left Ventricle	heart
3	chr1:92352400-92356600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:92352400-92356800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr1:92352400-92356800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:92352400-92357200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr1:92352400-92357400	Weak transcription	HSMMtube	muscle
8	chr1:92352400-92357400	Weak transcription	NH-A	brain
9	chr1:92352400-92357600	Weak transcription	Right Atrium	heart
10	chr1:92352400-92362600	Weak transcription	Psoas Muscle	Psoas
11	chr1:92352400-92366600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr1:92352600-92356800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr1:92352600-92356800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr1:92352600-92356800	Weak transcription	Fetal Stomach	stomach
15	chr1:92352600-92357000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr1:92352600-92357000	Weak transcription	HUVEC	blood vessel
17	chr1:92352600-92357200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr1:92352600-92357200	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr1:92352600-92357200	Weak transcription	Fetal Kidney	kidney
20	chr1:92352600-92357400	Weak transcription	Liver	Liver
21	chr1:92352600-92357600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:92352600-92357600	Weak transcription	Fetal Muscle Leg	muscle
23	chr1:92352600-92357600	Weak transcription	Spleen	Spleen
24	chr1:92352600-92362800	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr1:92352600-92370600	Weak transcription	K562	blood
26	chr1:92352800-92356800	Weak transcription	Adipose Nuclei	Adipose
27	chr1:92352800-92357600	Weak transcription	Ovary	ovary
28	chr1:92353000-92357800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:92354000-92357200	Enhancers	Placenta	Placenta
30	chr1:92354400-92357400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr1:92354800-92355800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr1:92354800-92355800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr1:92355000-92355800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:92355000-92357000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:92355200-92355800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr1:92355200-92355800	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr1:92355200-92355800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr1:92355200-92355800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr1:92355200-92355800	Flanking Active TSS	A549	lung
40	chr1:92355200-92355800	Flanking Active TSS	Hela-S3	cervix
41	chr1:92355200-92356200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:92355200-92356200	Enhancers	NHEK	skin
43	chr1:92355200-92356400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:92355200-92356400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr1:92355200-92356800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr1:92355200-92357200	Enhancers	Muscle Satellite Cultured Cells	--
47	chr1:92355200-92357200	Enhancers	GM12878-XiMat	blood
48	chr1:92355200-92357600	Enhancers	HepG2	liver
49	chr1:92355200-92358200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:92355200-92358200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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