Variant report

Variant	rs379471
Chromosome Location	chr9:136890649-136890650
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	SP1	chr9:136889725-136890667	H1-hESC	embryonic stem cell:	n/a	chr9:136890211-136890222 chr9:136890145-136890156 chr9:136890229-136890240 chr9:136890178-136890189 chr9:136890193-136890204 chr9:136890465-136890474
2	HDAC2	chr9:136890460-136890718	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr9:136890602-136890687	GM12878	blood:	n/a	n/a
4	POLR2A	chr9:136890465-136890723	GM12878	blood:	n/a	n/a
5	CHD2	chr9:136889973-136890692	GM12878	blood:	n/a	n/a
6	SRF	chr9:136890202-136890897	MCF-7	breast:	n/a	n/a
7	MYC	chr9:136890327-136890678	HUVEC	blood vessel:	n/a	n/a
8	JUND	chr9:136890217-136890677	GM12878	blood:	n/a	n/a
9	EP300	chr9:136890381-136890658	GM12878	blood:	n/a	n/a
10	POLR2A	chr9:136889800-136891179	H1-neurons	neurons:	n/a	n/a
11	IRF1	chr9:136889955-136890717	K562	blood:	n/a	n/a
12	SIN3AK20	chr9:136890241-136890887	PANC-1	pancreas:	n/a	n/a
13	JUN	chr9:136890006-136891110	K562	blood:	n/a	n/a
14	SP1	chr9:136890023-136890661	K562	blood:	n/a	chr9:136890211-136890222 chr9:136890145-136890156 chr9:136890229-136890240 chr9:136890178-136890189 chr9:136890193-136890204 chr9:136890465-136890474
15	POLR2A	chr9:136890458-136891010	MCF-7	breast:	n/a	n/a
16	MAX	chr9:136890041-136890769	H1-hESC	embryonic stem cell:	n/a	chr9:136890674-136890683
17	EP300	chr9:136890234-136890720	A549	lung:	n/a	n/a
18	POLR2A	chr9:136889710-136890868	HUVEC	blood vessel:	n/a	n/a
19	GATA3	chr9:136890342-136890680	T-47D	breast:	n/a	n/a
20	JUND	chr9:136889988-136890714	K562	blood:	n/a	n/a
21	PML	chr9:136890278-136890817	GM12878	blood:	n/a	n/a
22	ELK1	chr9:136890189-136890686	Hela-S3	cervix:	n/a	n/a
23	MXI1	chr9:136889604-136891651	SK-N-SH	brain:	n/a	n/a
24	POLR2A	chr9:136890445-136891017	K562	blood:	n/a	n/a
25	MXI1	chr9:136890334-136891241	GM12878	blood:	n/a	n/a
26	NR2C2	chr9:136890345-136890710	K562	blood:	n/a	n/a
27	NR2C2	chr9:136890314-136890739	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr9:136890459-136890991	GM12878	blood:	n/a	n/a
29	ZNF263	chr9:136889516-136890699	HEK293-T-REx	kidney:	n/a	chr9:136890183-136890204 chr9:136890219-136890240 chr9:136890147-136890168
30	SP1	chr9:136889794-136890846	A549	lung:	n/a	chr9:136890211-136890222 chr9:136890145-136890156 chr9:136890229-136890240 chr9:136890711-136890725 chr9:136890178-136890189 chr9:136890193-136890204 chr9:136890465-136890474
31	EP300	chr9:136890088-136890658	SK-N-SH_RA	brain:	n/a	n/a
32	SRF	chr9:136890200-136890684	GM12878	blood:	n/a	n/a
33	EP300	chr9:136890297-136890715	T-47D	breast:	n/a	n/a
34	SRF	chr9:136890265-136890713	H1-hESC	embryonic stem cell:	n/a	n/a
35	MYC	chr9:136890049-136891372	NB4	blood:	n/a	chr9:136890674-136890683
36	POLR2A	chr9:136890416-136890746	A549	lung:	n/a	n/a
37	YY1	chr9:136890340-136890710	SK-N-SH	brain:	n/a	n/a
38	MAX	chr9:136890249-136890775	HepG2	liver:	n/a	chr9:136890674-136890683
39	MXI1	chr9:136890334-136890747	Hela-S3	cervix:	n/a	n/a
40	SRF	chr9:136890296-136890708	K562	blood:	n/a	n/a
41	JUND	chr9:136890243-136890753	A549	lung:	n/a	n/a
42	TCF3	chr9:136890415-136890677	GM12878	blood:	n/a	n/a
43	MAX	chr9:136890295-136891209	SK-N-SH	brain:	n/a	chr9:136890674-136890683
44	YY1	chr9:136890410-136890713	H1-hESC	embryonic stem cell:	n/a	n/a
45	HDAC2	chr9:136890330-136890735	HepG2	liver:	n/a	n/a
46	MAX	chr9:136890240-136890969	HUVEC	blood vessel:	n/a	chr9:136890674-136890683
47	MXI1	chr9:136890010-136891159	HepG2	liver:	n/a	n/a
48	POLR2A	chr9:136890400-136890812	GM12892	blood:	n/a	n/a
49	RUNX3	chr9:136890352-136890734	GM12878	blood:	n/a	n/a
50	POLR2A	chr9:136890453-136890743	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:136890645..136892420-chr9:136892471..136894163,2	K562	blood:
2	chr9:136889824..136891845-chr9:137000522..137002324,2	K562	blood:
3	chr9:136890470..136892525-chr9:136914394..136917333,2	K562	blood:
4	chr9:136857193..136859735-chr9:136888278..136891342,4	MCF-7	breast:
5	chr9:136888954..136894255-chr9:136931474..136935040,9	K562	blood:
6	chr9:136888457..136893834-chr9:136930854..136936517,11	MCF-7	breast:
7	chr9:136889870..136892902-chr9:136892951..136894891,4	MCF-7	breast:
8	chr9:136889586..136891747-chr9:136893297..136895999,4	MCF-7	breast:
9	chr9:136889377..136892336-chr9:136904315..136908613,4	MCF-7	breast:
10	chr9:136888985..136892489-chr9:136929943..136933995,5	K562	blood:
11	chr9:136888792..136891646-chr9:137000403..137003499,3	MCF-7	breast:
12	chr9:136856335..136860882-chr9:136888369..136892368,8	MCF-7	breast:
13	chr9:136889327..136891768-chr9:136933108..136935436,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR5-3	chr9:136890608-136890658	ENSG00000235106
2	lnc-WDR5-3	chr9:136890561-136890658	NONHSAT135349

Variant related genes	Relation type
LINC00094	TF binding region
ENSG00000235106	Chromatin interaction
ENSG00000160293	Chromatin interaction
ENSG00000169925	Chromatin interaction
ENSG00000196363	Chromatin interaction
ENSG00000273249	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs109536	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10993894	0.84[AMR][1000 genomes]
rs10993895	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2073818	0.83[EUR][1000 genomes]
rs2519831	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2520094	0.84[EUR][1000 genomes]
rs2520095	0.84[EUR][1000 genomes]
rs2520096	0.80[EUR][1000 genomes]
rs2520099	0.83[EUR][1000 genomes]
rs2810480	0.84[ASN][1000 genomes]
rs2810489	0.83[EUR][1000 genomes]
rs2810491	0.82[EUR][1000 genomes]
rs3094339	0.83[AMR][1000 genomes]
rs378740	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs379417	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs386770	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs392134	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs401826	0.84[EUR][1000 genomes]
rs408307	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs410876	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs416390	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs433402	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs437182	0.86[ASN][1000 genomes]
rs448918	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs455073	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs455381	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs456205	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs456207	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs456793	0.84[ASN][1000 genomes]
rs459571	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs460154	0.85[EUR][1000 genomes]
rs460888	0.84[EUR][1000 genomes]
rs461462	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs465535	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs465724	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs466681	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs467303	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs467379	0.85[ASN][1000 genomes]
rs467387	0.84[EUR][1000 genomes]
rs55923934	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][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	nsv894125	chr9:136723520-136931957	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv894128	chr9:136753246-136906752	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv894130	chr9:136767346-136906752	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS 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	25 gene(s)	inside rSNPs	diseases
4	nsv831748	chr9:136788484-136944326	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv894131	chr9:136792765-136906752	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer 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 target site	25 gene(s)	inside rSNPs	diseases
6	nsv831749	chr9:136809200-136915764	Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
7	nsv894132	chr9:136813341-136950691	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
8	nsv428226	chr9:136825035-136994606	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
9	nsv894134	chr9:136839840-136892523	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
10	nsv894135	chr9:136839840-136927657	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
11	nsv894136	chr9:136839840-136938961	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	nsv894137	chr9:136839840-136950691	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
13	nsv894138	chr9:136839840-137093168	Strong transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
14	nsv825148	chr9:136848471-137025632	Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
15	nsv894139	chr9:136863932-136950691	Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
16	nsv894140	chr9:136865879-136927657	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS 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	12 gene(s)	inside rSNPs	diseases
17	nsv894141	chr9:136865879-136938961	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	nsv894142	chr9:136870787-136906752	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
19	nsv466627	chr9:136870787-136938961	Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
20	nsv615774	chr9:136870787-136938961	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
21	nsv1048571	chr9:136872166-137265444	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
22	nsv894143	chr9:136874066-136906752	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
23	nsv894144	chr9:136874066-136909261	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
24	nsv894145	chr9:136874066-136925451	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
25	nsv894146	chr9:136874066-136938961	Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
26	nsv894147	chr9:136874066-136950691	Enhancers Genic enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
27	nsv894148	chr9:136874066-137093168	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
28	nsv894149	chr9:136874158-136950691	Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
29	nsv894150	chr9:136887757-136944827	ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
30	nsv894151	chr9:136887757-137397609	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136889400-136890800	Enhancers	Placenta	Placenta
2	chr9:136889400-136891200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:136889400-136891200	Active TSS	Brain Cingulate Gyrus	brain
4	chr9:136889400-136891400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:136889600-136890800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr9:136889600-136890800	Active TSS	Brain Hippocampus Middle	brain
7	chr9:136889600-136890800	Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr9:136889600-136891200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:136889600-136891200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr9:136889600-136891200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr9:136889600-136891200	Active TSS	Brain Anterior Caudate	brain
12	chr9:136889600-136891200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr9:136889600-136891200	Active TSS	Fetal Lung	lung
14	chr9:136889600-136891200	Active TSS	Rectal Smooth Muscle	rectum
15	chr9:136889600-136891200	Active TSS	GM12878-XiMat	blood
16	chr9:136889600-136891200	Active TSS	NHEK	skin
17	chr9:136889600-136891400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:136889600-136891400	Active TSS	NHDF-Ad	bronchial
19	chr9:136889600-136891600	Active TSS	A549	lung
20	chr9:136889600-136891800	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr9:136889600-136891800	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr9:136889800-136890800	Active TSS	Duodenum Mucosa	Duodenum
23	chr9:136889800-136890800	Active TSS	Stomach Smooth Muscle	stomach
24	chr9:136889800-136890800	Active TSS	Monocytes-CD14+_RO01746	blood
25	chr9:136889800-136891000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr9:136889800-136891000	Active TSS	Brain Substantia Nigra	brain
27	chr9:136889800-136891000	Active TSS	Fetal Muscle Leg	muscle
28	chr9:136889800-136891000	Active TSS	Fetal Stomach	stomach
29	chr9:136889800-136891200	Active TSS	H1 Cell Line	embryonic stem cell
30	chr9:136889800-136891200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr9:136889800-136891200	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr9:136889800-136891200	Active TSS	Fetal Intestine Small	intestine
33	chr9:136889800-136891200	Active TSS	Ovary	ovary
34	chr9:136889800-136891200	Active TSS	Right Ventricle	heart
35	chr9:136889800-136891200	Active TSS	Thymus	Thymus
36	chr9:136889800-136891200	Active TSS	HSMMtube	muscle
37	chr9:136889800-136891200	Active TSS	HUVEC	blood vessel
38	chr9:136889800-136891200	Active TSS	NH-A	brain
39	chr9:136889800-136891200	Active TSS	NHLF	lung
40	chr9:136889800-136891400	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr9:136889800-136891400	Active TSS	Brain Angular Gyrus	brain
42	chr9:136889800-136891400	Active TSS	HSMM	muscle
43	chr9:136889800-136891600	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr9:136889800-136892000	Active TSS	H9 Cell Line	embryonic stem cell
45	chr9:136890000-136890800	Active TSS	Liver	Liver
46	chr9:136890000-136891000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr9:136890000-136891000	Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr9:136890000-136891000	Active TSS	Colonic Mucosa	Colon
49	chr9:136890000-136891000	Active TSS	Fetal Brain Female	brain
50	chr9:136890000-136891200	Active TSS	Breast Myoepithelial Primary Cells	Breast

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