Variant report

Variant	rs1766862
Chromosome Location	chr1:113615193-113615194
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	CBX3	chr1:113614710-113616713	K562	blood:	n/a	n/a
2	ARID3A	chr1:113614699-113615830	K562	blood:	n/a	n/a
3	ATF1	chr1:113614716-113615966	K562	blood:	n/a	n/a
4	CTCF	chr1:113615144-113615835	K562	blood:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
5	ZKSCAN1	chr1:113615008-113616338	Hela-S3	cervix:	n/a	n/a
6	GATA3	chr1:113615117-113615557	MCF-7	breast:	n/a	n/a
7	GATA3	chr1:113615036-113615579	SH-SY5Y	brain:	n/a	n/a
8	CEBPB	chr1:113614761-113615472	IMR90	lung:	n/a	chr1:113614859-113614870
9	SMARCB1	chr1:113614679-113616267	K562	blood:	n/a	n/a
10	GATA3	chr1:113615077-113615951	T-47D	breast:	n/a	n/a
11	TEAD4	chr1:113615129-113616422	K562	blood:	n/a	n/a
12	RAD21	chr1:113615094-113616039	ECC-1	luminal epithelium:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615124-113615133 chr1:113615387-113615400 chr1:113615389-113615401
13	RCOR1	chr1:113614768-113616833	K562	blood:	n/a	n/a
14	CTCF	chr1:113615156-113615785	HepG2	liver:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
15	YY1	chr1:113615137-113616358	HCT-116	colon:	n/a	n/a
16	POLR2A	chr1:113615181-113616737	K562	blood:	n/a	n/a
17	MYBL2	chr1:113615039-113616122	HepG2	liver:	n/a	n/a
18	RCOR1	chr1:113615127-113616263	GM12878	blood:	n/a	n/a
19	POLR2A	chr1:113614912-113616753	K562	blood:	n/a	n/a
20	CTCF	chr1:113615191-113615778	T-47D	breast:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
21	RAD21	chr1:113615154-113615881	ECC-1	luminal epithelium:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615387-113615400 chr1:113615389-113615401
22	CTCF	chr1:113614616-113616959	SK-N-SH	brain:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
23	CTCF	chr1:113615189-113615785	SK-N-SH_RA	brain:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
24	RAD21	chr1:113615186-113616428	IMR90	lung:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615387-113615400 chr1:113615389-113615401
25	RAD21	chr1:113615064-113615925	H1-hESC	embryonic stem cell:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615124-113615133 chr1:113615387-113615400 chr1:113615389-113615401
26	KAP1	chr1:113614926-113616457	HEK293	kidney:	n/a	n/a
27	CHD2	chr1:113615133-113616413	GM12878	blood:	n/a	n/a
28	MAX	chr1:113615138-113616478	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr1:113615055-113616516	MCF-7	breast:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
30	TAL1	chr1:113614718-113616753	K562	blood:	n/a	n/a
31	BCLAF1	chr1:113615116-113616194	GM12878	blood:	n/a	n/a
32	POLR2A	chr1:113615118-113616530	SK-N-MC	brain:	n/a	n/a
33	JUND	chr1:113614780-113616383	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr1:113615190-113615857	A549	lung:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
35	SMC3	chr1:113615010-113616430	K562	blood:	n/a	chr1:113615389-113615399 chr1:113615385-113615399
36	CTCF	chr1:113615181-113615842	H1-hESC	embryonic stem cell:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
37	POU2F2	chr1:113615022-113616072	GM12878	blood:	n/a	chr1:113615334-113615342 chr1:113615331-113615346 chr1:113615334-113615343 chr1:113615329-113615347 chr1:113615332-113615343 chr1:113615334-113615344 chr1:113615333-113615343 chr1:113615335-113615342
38	FOXA2	chr1:113615161-113615506	HepG2	liver:	n/a	n/a
39	SP1	chr1:113615099-113616061	H1-hESC	embryonic stem cell:	n/a	chr1:113615378-113615399 chr1:113615810-113615819
40	SIN3AK20	chr1:113615164-113616475	H1-hESC	embryonic stem cell:	n/a	n/a
41	SIN3AK20	chr1:113615174-113616018	SK-N-SH	brain:	n/a	n/a
42	SP4	chr1:113615166-113615860	H1-hESC	embryonic stem cell:	n/a	n/a
43	GATA3	chr1:113615115-113615815	T-47D	breast:	n/a	n/a
44	CEBPD	chr1:113614650-113616514	K562	blood:	n/a	n/a
45	RAD21	chr1:113615102-113615948	A549	lung:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615124-113615133 chr1:113615387-113615400 chr1:113615389-113615401
46	POLR2A	chr1:113615030-113616520	H1-hESC	embryonic stem cell:	n/a	n/a
47	GATA2	chr1:113615028-113615777	HUVEC	blood vessel:	n/a	n/a
48	POU2F2	chr1:113615171-113615546	GM12878	blood:	n/a	chr1:113615334-113615342 chr1:113615331-113615346 chr1:113615334-113615343 chr1:113615329-113615347 chr1:113615332-113615343 chr1:113615334-113615344 chr1:113615333-113615343 chr1:113615335-113615342
49	CTCF	chr1:113614771-113616621	HCT-116	colon:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
50	MAZ	chr1:113615043-113616927	IMR90	lung:	n/a	chr1:113616695-113616703 chr1:113616690-113616703

No.	Distal block	Cell Line	Cell type
1	chr1:113614064..113616964-chr1:113668302..113669880,2	K562	blood:
2	chr1:113613175..113615596-chr1:113621813..113624852,3	K562	blood:
3	chr1:113493791..113500715-chr1:113613796..113618010,15	K562	blood:
4	chr1:113257532..113261488-chr1:113614794..113617265,4	K562	blood:
5	chr1:113495059..113500488-chr1:113613593..113618010,11	K562	blood:
6	chr1:113610863..113612583-chr1:113613310..113615320,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC16A1-2	chr1:113614707-113615830	NONHSAT005314

Variant related genes	Relation type
LRIG2	TF binding region
ENSG00000226419	Chromatin interaction
ENSG00000237278	Chromatin interaction
ENSG00000261595	Chromatin interaction
ENSG00000155367	Chromatin interaction
ENSG00000155380	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs11102575	0.80[CEU][hapmap];0.94[JPT][hapmap]
rs11102576	0.80[CEU][hapmap];0.94[JPT][hapmap]
rs11102577	0.85[ASN][1000 genomes]
rs11102578	0.93[ASN][1000 genomes]
rs11102579	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11102581	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11102582	1.00[CEU][hapmap];0.93[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12140104	0.93[ASN][1000 genomes]
rs1216760	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1216762	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1216763	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216766	0.93[ASN][1000 genomes]
rs1216768	0.91[EUR][1000 genomes]
rs1216772	0.94[JPT][hapmap]
rs1216780	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1216781	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1216783	0.94[JPT][hapmap]
rs1216790	0.85[ASN][1000 genomes]
rs1216801	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1216804	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12184285	0.94[JPT][hapmap]
rs12568813	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs12744009	1.00[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12746771	0.80[CEU][hapmap];0.94[JPT][hapmap]
rs12758163	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1419136	0.93[ASN][1000 genomes]
rs1544227	0.94[JPT][hapmap]
rs1619133	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1626085	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17030905	0.81[CHD][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap]
rs17030974	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1728218	0.94[JPT][hapmap]
rs1728230	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1728238	0.92[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1766863	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1766866	0.82[ASN][1000 genomes]
rs1778015	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1778018	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1778024	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1778025	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1778027	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1778028	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1983929	0.94[JPT][hapmap]
rs2485964	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2798686	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2798687	0.93[ASN][1000 genomes]
rs2798689	0.93[ASN][1000 genomes]
rs2840294	0.88[CEU][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs3889656	0.83[CEU][hapmap];0.86[JPT][hapmap]
rs3951437	0.85[ASN][1000 genomes]
rs4025965	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4838975	0.93[ASN][1000 genomes]
rs55894203	0.89[ASN][1000 genomes]
rs6656311	0.80[CEU][hapmap];0.94[JPT][hapmap]
rs72683488	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9429509	0.93[ASN][1000 genomes]
rs9787311	0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002971	chr1:112924725-113740584	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv535059	chr1:112924725-113740584	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv1010276	chr1:113123932-113740584	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv1012119	chr1:113214869-113759081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
5	nsv535060	chr1:113214869-113759081	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv529238	chr1:113229946-113759080	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
7	nsv997426	chr1:113288282-113639507	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic 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	68 gene(s)	inside rSNPs	diseases
8	nsv999915	chr1:113360145-113684833	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
9	esv18293	chr1:113375437-113852815	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
10	nsv1007045	chr1:113425222-113839910	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv946146	chr1:113567302-113640814	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	nsv427719	chr1:113570229-114078388	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
13	nsv508537	chr1:113590343-113635803	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	nsv437002	chr1:113592588-113658887	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
15	nsv435694	chr1:113610263-113616294	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs1766862	LOC149620	cis	cerebellum	SCAN
rs1766862	GPR3	trans	parietal	SCAN
rs1766862	KCNA10	cis	parietal	SCAN
rs1766862	LRIG2	cis	parietal	SCAN
rs1766862	SLC6A17	cis	parietal	SCAN

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113614400-113615200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr1:113614600-113615200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:113614600-113615200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr1:113614600-113615200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr1:113614600-113615200	Enhancers	Primary B cells from cord blood	blood
6	chr1:113614600-113615200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr1:113614600-113615400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr1:113614600-113615400	Flanking Active TSS	HepG2	liver
9	chr1:113614800-113615200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
10	chr1:113614800-113615200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr1:113614800-113615200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr1:113614800-113615200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr1:113614800-113615200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr1:113614800-113615200	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr1:113614800-113615200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr1:113614800-113615200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
17	chr1:113614800-113615200	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr1:113614800-113615200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr1:113614800-113615200	Flanking Active TSS	Brain Anterior Caudate	brain
20	chr1:113614800-113615200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:113614800-113615200	Enhancers	Colon Smooth Muscle	Colon
22	chr1:113614800-113615200	Flanking Active TSS	Fetal Brain Female	brain
23	chr1:113614800-113615200	Flanking Active TSS	Fetal Heart	heart
24	chr1:113614800-113615200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr1:113614800-113615200	Enhancers	Small Intestine	intestine
26	chr1:113614800-113615200	Enhancers	Stomach Mucosa	stomach
27	chr1:113614800-113615200	Flanking Active TSS	GM12878-XiMat	blood
28	chr1:113614800-113615200	Enhancers	HSMM	muscle
29	chr1:113614800-113615400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:113614800-113615400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr1:113614800-113615400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:113614800-113615400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
33	chr1:113614800-113615400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:113614800-113615400	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr1:113614800-113615400	Flanking Active TSS	Liver	Liver
36	chr1:113614800-113615400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
37	chr1:113614800-113615400	Flanking Active TSS	Brain Substantia Nigra	brain
38	chr1:113614800-113615400	Flanking Active TSS	Duodenum Mucosa	Duodenum
39	chr1:113614800-113615400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
40	chr1:113614800-113615400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr1:113614800-113615400	Flanking Active TSS	Dnd41	blood
42	chr1:113614800-113615400	Flanking Active TSS	Hela-S3	cervix
43	chr1:113614800-113615400	Flanking Active TSS	K562	blood
44	chr1:113614800-113615600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
45	chr1:113614800-113615600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr1:113614800-113616600	Active TSS	Brain Hippocampus Middle	brain
47	chr1:113614800-113617000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr1:113614800-113617200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr1:113615000-113615200	Flanking Active TSS	H9 Cell Line	embryonic stem cell
50	chr1:113615000-113615200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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