Variant report

Variant	rs537988909
Chromosome Location	chr15:99645057-99645058
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	EP300	chr15:99644899-99645327	SK-N-SH_RA	brain:	n/a	chr15:99645292-99645308
2	RAD21	chr15:99644950-99645352	H1-hESC	embryonic stem cell:	n/a	chr15:99645127-99645140 chr15:99645149-99645161 chr15:99645149-99645159
3	ZBTB7A	chr15:99644918-99645265	ECC-1	luminal epithelium:	n/a	chr15:99645151-99645160
4	MAX	chr15:99644978-99646005	HepG2	liver:	n/a	chr15:99645146-99645156
5	CTCF	chr15:99644947-99645174	K562	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
6	EBF1	chr15:99644993-99645266	GM12878	blood:	n/a	n/a
7	CTCF	chr15:99645040-99645190	HepG2	liver:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
8	CTCF	chr15:99645040-99645190	HPF	lung:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
9	TCF3	chr15:99644962-99645349	GM12878	blood:	n/a	chr15:99645122-99645136
10	CTCF	chr15:99645040-99645190	AG04450	lung:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
11	CTCF	chr15:99644960-99645301	MCF-7	breast:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
12	CTCF	chr15:99644964-99645278	A549	lung:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
13	TBP	chr15:99644932-99645493	H1-hESC	embryonic stem cell:	n/a	n/a
14	MAX	chr15:99644834-99646274	HepG2	liver:	n/a	chr15:99645146-99645156
15	CTCF	chr15:99644850-99645359	A549	lung:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
16	TEAD4	chr15:99645042-99645345	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr15:99644871-99645378	H1-hESC	embryonic stem cell:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
18	PBX3	chr15:99644991-99645611	A549	lung:	n/a	chr15:99645193-99645202
19	CTCF	chr15:99644976-99645269	K562	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
20	CTCF	chr15:99645007-99645259	K562	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
21	CTCF	chr15:99644937-99645298	SK-N-SH_RA	brain:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
22	HEY1	chr15:99645020-99645550	HepG2	liver:	n/a	chr15:99645307-99645322
23	CTCF	chr15:99645040-99645190	WERI-Rb-1	eye:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
24	CTCF	chr15:99645040-99645190	GM12865	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
25	CTCF	chr15:99645040-99645190	AG09309	skin:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
26	CTCF	chr15:99644989-99645260	HepG2	liver:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
27	MAX	chr15:99644908-99645534	SK-N-SH	brain:	n/a	chr15:99645146-99645156
28	TAF1	chr15:99645035-99645532	H1-hESC	embryonic stem cell:	n/a	n/a
29	RAD21	chr15:99644974-99645293	GM12878	blood:	n/a	chr15:99645127-99645140 chr15:99645149-99645161 chr15:99645149-99645159
30	UBTF	chr15:99644986-99645446	K562	blood:	n/a	n/a
31	RAD21	chr15:99644920-99645412	IMR90	lung:	n/a	chr15:99645127-99645140 chr15:99645149-99645161 chr15:99645149-99645159
32	E2F6	chr15:99644981-99646636	H1-hESC	embryonic stem cell:	n/a	chr15:99645503-99645511 chr15:99645194-99645203 chr15:99645093-99645102 chr15:99646410-99646420
33	TCF12	chr15:99644997-99645379	GM12878	blood:	n/a	chr15:99645357-99645367 chr15:99645142-99645149
34	CREB1	chr15:99644870-99646275	A549	lung:	n/a	n/a
35	CTCF	chr15:99645020-99645170	GM12868	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
36	MXI1	chr15:99644988-99645767	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:99645038-99645173	HepG2	liver:	n/a	n/a
38	CTCF	chr15:99644980-99645130	AG04450	lung:	n/a	n/a
39	SMC3	chr15:99644963-99645301	HepG2	liver:	n/a	chr15:99645149-99645159
40	CTCF	chr15:99645020-99645170	HRE	kidney:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
41	ZNF263	chr15:99645045-99646271	HEK293-T-REx	kidney:	n/a	n/a
42	CTCF	chr15:99645020-99645170	HA-sp	spinal cord:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
43	UBTF	chr15:99644955-99645276	K562	blood:	n/a	n/a
44	CTCF	chr15:99645000-99645150	HCFaa	heart:	n/a	chr15:99645126-99645139
45	POLR2A	chr15:99645040-99645606	Gliobla	brain:	n/a	n/a
46	SMARCB1	chr15:99644931-99646559	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr15:99645040-99645190	GM12869	blood:	n/a	chr15:99645144-99645160 chr15:99645126-99645139 chr15:99645146-99645159
48	MXI1	chr15:99645021-99645434	Hela-S3	cervix:	n/a	n/a
49	RCOR1	chr15:99645015-99645286	GM12878	blood:	n/a	n/a
50	RAD21	chr15:99644838-99645350	SK-N-SH_RA	brain:	n/a	chr15:99645127-99645140 chr15:99645149-99645161 chr15:99645149-99645159

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:99645031-99645081	AG10803	skin:	n/a
2	chr15:99645031-99645081	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:99645031-99645081	HAEpiC	amniotic membrane:	n/a
4	chr15:99645031-99645081	AG09319	gingival:	n/a
5	chr15:99645031-99645081	U87	brain:	n/a
6	chr15:99645031-99645081	Jurkat	blood:	n/a
7	chr15:99645031-99645081	AG09309	skin:	n/a
8	chr15:99645031-99645081	GM12878	blood:	n/a
9	chr15:99645031-99645081	MCF10A-Er-Src	breast:	n/a
10	chr15:99645031-99645081	K562	blood:	n/a
11	chr15:99645031-99645081	HNPCEpiC	eye:	n/a
12	chr15:99645031-99645081	HepG2	liver:	n/a
13	chr15:99645031-99645081	Hepatocyte	liver:	n/a
14	chr15:99645031-99645081	SK-N-SH_RA	brain:	n/a
15	chr15:99645031-99645081	HRCEpiC	kidney:	n/a
16	chr15:99645031-99645081	SK-N-SH	brain:	n/a
17	chr15:99645031-99645081	GM12892	blood:	n/a
18	chr15:99645031-99645081	HCPEpiC	choroid plexus:	n/a
19	chr15:99645031-99645081	ovcar-3	ovarian:	n/a
20	chr15:99645031-99645081	PrEC	prostate:	n/a
21	chr15:99645031-99645081	Hela-S3	cervix:	n/a
22	chr15:99645031-99645081	HCT-116	colon:	n/a
23	chr15:99645031-99645081	RPTEC	kidney:	n/a
24	chr15:99645031-99645081	MCF-7	breast:	n/a
25	chr15:99645031-99645081	PANC-1	pancreas:	n/a
26	chr15:99645031-99645081	NHDF-neo	bronchial:	n/a
27	chr15:99645031-99645081	HMEC	breast:	n/a
28	chr15:99645031-99645081	GM06990	blood:	n/a
29	chr15:99645031-99645081	LNCaP	prostate:	n/a
30	chr15:99645031-99645081	NH-A	brain:	n/a
31	chr15:99645031-99645081	SKMC	muscle:	n/a
32	chr15:99645031-99645081	ProgFib	skin:	n/a
33	chr15:99645031-99645081	SAEC	small airway:	n/a
34	chr15:99645031-99645081	CMK	blood:	n/a
35	chr15:99645031-99645081	GM19239	blood:	n/a
36	chr15:99645031-99645081	T-47D	breast:	n/a
37	chr15:99645031-99645081	AoSMC	blood vessel:	n/a
38	chr15:99645031-99645081	H1-hESC	embryonic stem cell:	embryo
39	chr15:99645031-99645081	HIPEpiC	eye:	n/a
40	chr15:99645031-99645081	HL-60	blood:	n/a
41	chr15:99645031-99645081	GM12891	blood:	n/a
42	chr15:99645031-99645081	PFSK-1	brain:	n/a
43	chr15:99645031-99645081	A549	lung:	n/a
44	chr15:99645031-99645081	HEEpiC	esophagus:	n/a
45	chr15:99645031-99645081	Caco-2	colon:	n/a
46	chr15:99645031-99645081	HCF	heart:	n/a
47	chr15:99645031-99645081	HCM	heart:	n/a
48	chr15:99645031-99645081	BJ	skin:	n/a
49	chr15:99645031-99645081	ECC-1	luminal epithelium:	n/a
50	chr15:99645031-99645081	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:99644709..99645388-chr15:99791744..99792284,2	MCF-7	breast:
2	chr15:99643812..99646594-chr15:99789555..99792592,4	MCF-7	breast:

Variant related genes	Relation type
SYNM	TF binding region
SYNM	CpG island
ENSG00000103852	Chromatin interaction
ENSG00000168904	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531079	chr15:98907913-99878547	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv1039575	chr15:98982045-99924685	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription 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 miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv869529	chr15:99416774-99903351	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv533375	chr15:99443534-99696221	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1050982	chr15:99450004-99725825	Enhancers Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS 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	26 gene(s)	inside rSNPs	diseases
6	nsv530685	chr15:99452377-99713365	Bivalent/Poised TSS Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv1055008	chr15:99477144-100019861	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
8	nsv1045124	chr15:99504843-99847210	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv1038870	chr15:99510479-99768374	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
10	nsv904543	chr15:99513231-99991506	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
11	nsv533926	chr15:99519820-99997114	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
12	nsv915926	chr15:99519820-100138705	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
13	nsv904544	chr15:99524865-99655744	Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
14	nsv1051782	chr15:99621061-99792967	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
15	nsv916822	chr15:99621061-99878564	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	30 gene(s)	inside rSNPs	diseases
16	nsv949203	chr15:99621061-99932797	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats 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	31 gene(s)	inside rSNPs	diseases
17	nsv817289	chr15:99621061-100138705	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
18	nsv431411	chr15:99621061-100143999	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised 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	44 gene(s)	inside rSNPs	diseases
19	nsv570716	chr15:99629901-99916332	Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
20	esv3364884	chr15:99643929-99647227	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	esv20801	chr15:99644218-99646022	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99641000-99645200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:99641000-99645200	Weak transcription	Gastric	stomach
3	chr15:99641200-99645200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr15:99641200-99645200	Weak transcription	Colon Smooth Muscle	Colon
5	chr15:99641200-99645400	Weak transcription	Brain Substantia Nigra	brain
6	chr15:99643000-99645200	Weak transcription	A549	lung
7	chr15:99643400-99645200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr15:99643800-99645200	Weak transcription	Psoas Muscle	Psoas
9	chr15:99644000-99645200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:99644800-99645200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr15:99644800-99645200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
12	chr15:99644800-99645200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr15:99644800-99645200	Bivalent Enhancer	Fetal Thymus	thymus
14	chr15:99644800-99645400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
15	chr15:99644800-99645600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr15:99644800-99646000	Active TSS	Stomach Smooth Muscle	stomach
17	chr15:99644800-99646000	Active TSS	HepG2	liver
18	chr15:99644800-99646200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr15:99644800-99646200	Enhancers	Liver	Liver
20	chr15:99644800-99646200	Active TSS	Hela-S3	cervix
21	chr15:99644800-99646400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr15:99644800-99646600	Active TSS	NHLF	lung
23	chr15:99644800-99646600	Active TSS	Osteobl	bone
24	chr15:99644800-99646800	Active TSS	Brain Angular Gyrus	brain
25	chr15:99644800-99647200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr15:99645000-99645200	Enhancers	Primary B cells from cord blood	blood
27	chr15:99645000-99645200	Enhancers	Primary T cells from cord blood	blood
28	chr15:99645000-99645200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr15:99645000-99645200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr15:99645000-99645200	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
31	chr15:99645000-99645200	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr15:99645000-99645200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr15:99645000-99645200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr15:99645000-99645200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:99645000-99645200	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
36	chr15:99645000-99645200	Active TSS	Adipose Nuclei	Adipose
37	chr15:99645000-99645200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
38	chr15:99645000-99645200	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
39	chr15:99645000-99645200	Enhancers	Ovary	ovary
40	chr15:99645000-99645200	Enhancers	Pancreas	Pancrea
41	chr15:99645000-99645200	Flanking Active TSS	Right Ventricle	heart
42	chr15:99645000-99645200	Enhancers	GM12878-XiMat	blood
43	chr15:99645000-99645200	Flanking Bivalent TSS/Enh	NHEK	skin
44	chr15:99645000-99645400	Active TSS	Fetal Stomach	stomach
45	chr15:99645000-99645400	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr15:99645000-99645600	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
47	chr15:99645000-99645600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr15:99645000-99645800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr15:99645000-99645800	Active TSS	Sigmoid Colon	Sigmoid Colon
50	chr15:99645000-99645800	Active TSS	Skeletal Muscle Female	skeletal muscle

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