Variant report

Variant	rs7512552
Chromosome Location	chr1:150265704-150265705
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:150265703-150266738	K562	blood:	n/a	n/a
2	ELF1	chr1:150265658-150266874	MCF-7	breast:	n/a	chr1:150266267-150266280
3	GABPA	chr1:150265304-150267140	MCF-7	breast:	n/a	chr1:150266265-150266272
4	HCFC1	chr1:150265340-150267216	Hela-S3	cervix:	n/a	n/a
5	REST	chr1:150265590-150267098	H1-neurons	neurons:	n/a	n/a
6	SIN3AK20	chr1:150265531-150267163	MCF-7	breast:	n/a	n/a
7	GABPA	chr1:150265667-150266886	A549	lung:	n/a	chr1:150266265-150266272
8	POLR2A	chr1:150265687-150266965	PFSK-1	brain:	n/a	n/a
9	NR2F2	chr1:150265677-150267021	K562	blood:	n/a	n/a
10	POLR2A	chr1:150265583-150267205	H1-hESC	embryonic stem cell:	n/a	n/a
11	RCOR1	chr1:150265629-150266530	K562	blood:	n/a	n/a
12	TCF12	chr1:150265671-150266813	A549	lung:	n/a	n/a
13	MXI1	chr1:150265457-150267310	SK-N-SH	brain:	n/a	n/a
14	BACH1	chr1:150265694-150266201	K562	blood:	n/a	n/a

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150264700..150268461-chr1:150290358..150296338,12	MCF-7	breast:
2	chr1:150263378..150268409-chr1:150334980..150339088,9	MCF-7	breast:
3	chr1:150264985..150267116-chr1:150337062..150338980,2	MCF-7	breast:
4	chr1:150240223..150242953-chr1:150263372..150266971,3	K562	blood:
5	chr1:150264496..150269056-chr1:150292330..150296241,7	MCF-7	breast:
6	chr1:150206794..150209349-chr1:150261451..150266044,4	K562	blood:
7	chr1:150240546..150242221-chr1:150264940..150266566,2	K562	blood:
8	chr1:150234315..150237513-chr1:150265191..150267090,3	K562	blood:
9	chr1:150264617..150266703-chr1:150314248..150316568,2	MCF-7	breast:
10	chr1:149855825..149859735-chr1:150264985..150268023,4	MCF-7	breast:
11	chr1:150264361..150267747-chr1:150292578..150295568,3	K562	blood:
12	chr1:150265074..150268122-chr1:150334427..150338986,4	K562	blood:
13	chr1:150205825..150209635-chr1:150259375..150267858,10	K562	blood:
14	chr1:150265031..150267516-chr1:150292699..150295000,3	K562	blood:
15	chr1:150265389..150267976-chr1:150336270..150338986,2	K562	blood:
16	chr1:150206170..150208675-chr1:150264452..150269195,6	MCF-7	breast:

No data

Variant related genes	Relation type
MRPS21	TF binding region
ENSG00000184260	Chromatin interaction
ENSG00000117362	Chromatin interaction
ENSG00000163125	Chromatin interaction
ENSG00000143401	Chromatin interaction
ENSG00000222222	Chromatin interaction
ENSG00000118292	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000117360	Chromatin interaction
ENSG00000118298	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000184678	Chromatin interaction

Extended variants
information (count: 151 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:147)

rs_ID	r²[population]
rs10788873	0.92[CEU][hapmap];0.92[EUR][1000 genomes]
rs10888578	0.83[GIH][hapmap]
rs1097067	0.82[ASN][1000 genomes]
rs1097068	0.82[ASN][1000 genomes]
rs1097070	0.82[ASN][1000 genomes]
rs1103115	0.85[ASN][1000 genomes]
rs11205354	0.89[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap]
rs11205357	1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11205359	0.95[ASN][1000 genomes]
rs11205373	0.87[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs1122967	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1145583	0.85[ASN][1000 genomes]
rs11577600	0.80[ASN][1000 genomes]
rs11577843	0.93[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs11581351	0.93[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap]
rs11587575	0.92[CHB][hapmap];0.94[JPT][hapmap]
rs11587758	0.85[ASN][1000 genomes]
rs11590787	0.81[ASN][1000 genomes]
rs12028001	0.80[ASN][1000 genomes]
rs12029359	0.86[CHB][hapmap]
rs12040949	0.93[CHB][hapmap];0.94[JPT][hapmap]
rs12045304	0.81[ASN][1000 genomes]
rs12046899	0.86[CHB][hapmap]
rs1260367	0.93[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs1260368	0.85[ASN][1000 genomes]
rs1260386	0.81[ASN][1000 genomes]
rs1260388	0.81[ASN][1000 genomes]
rs1260389	0.81[ASN][1000 genomes]
rs1260394	0.81[AMR][1000 genomes]
rs1260396	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1260398	0.95[ASN][1000 genomes]
rs1260400	0.84[ASN][1000 genomes]
rs1260404	0.86[ASN][1000 genomes]
rs1260405	0.85[ASN][1000 genomes]
rs1260406	0.85[ASN][1000 genomes]
rs1260407	0.93[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs1260409	0.84[ASN][1000 genomes]
rs1260411	0.93[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs1260421	0.81[ASN][1000 genomes]
rs1260458	0.85[ASN][1000 genomes]
rs1260459	0.93[CHB][hapmap];0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs12747669	0.83[ASN][1000 genomes]
rs1313570	0.85[ASN][1000 genomes]
rs1498308	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.86[MEX][hapmap];0.86[MKK][hapmap];0.87[ASN][1000 genomes]
rs1614039	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1625468	0.87[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap];0.85[ASN][1000 genomes]
rs1627235	0.81[ASN][1000 genomes]
rs1694362	0.81[ASN][1000 genomes]
rs1694364	0.87[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs1694369	0.85[ASN][1000 genomes]
rs1694370	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1694375	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1694377	1.00[CHB][hapmap];0.94[JPT][hapmap];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1694379	0.84[GIH][hapmap]
rs1694380	0.93[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs1694381	0.90[ASN][1000 genomes]
rs1694385	0.81[ASN][1000 genomes]
rs1747927	0.89[ASN][1000 genomes]
rs17596326	0.93[CHB][hapmap];0.94[JPT][hapmap]
rs1776273	0.93[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap];0.97[ASN][1000 genomes]
rs1776274	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1776276	0.87[ASN][1000 genomes]
rs1932934	0.87[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap]
rs2147324	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];0.94[JPT][hapmap];0.91[TSI][hapmap];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2264418	0.81[ASN][1000 genomes]
rs2274127	0.92[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2318761	0.85[ASN][1000 genomes]
rs2454285	0.88[ASN][1000 genomes]
rs2454286	0.82[ASN][1000 genomes]
rs2477121	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2762860	0.93[ASN][1000 genomes]
rs2794614	0.80[ASN][1000 genomes]
rs2794615	0.81[ASN][1000 genomes]
rs2794678	0.85[ASN][1000 genomes]
rs2794679	0.92[CHB][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs2794681	0.93[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs2794682	0.83[ASN][1000 genomes]
rs2794684	0.84[ASN][1000 genomes]
rs2794685	0.85[ASN][1000 genomes]
rs2797653	0.85[ASN][1000 genomes]
rs2873669	0.93[CHB][hapmap];0.96[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap]
rs3125808	0.86[ASN][1000 genomes]
rs35057759	0.81[ASN][1000 genomes]
rs35915849	0.82[ASN][1000 genomes]
rs4333886	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4446975	0.87[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.88[JPT][hapmap];0.83[MEX][hapmap]
rs4451552	0.87[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap]
rs4581308	1.00[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs471464	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs471738	0.93[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs486275	0.89[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.94[LWK][hapmap];0.90[MEX][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs488271	0.93[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs4926394	0.81[ASN][1000 genomes]
rs4926395	0.87[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs4926419	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4926422	0.86[ASN][1000 genomes]
rs494041	0.81[ASN][1000 genomes]
rs494952	0.84[ASN][1000 genomes]
rs4970922	0.86[GIH][hapmap]
rs497128	0.88[ASN][1000 genomes]
rs500812	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs509345	0.93[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.81[MKK][hapmap];0.94[ASN][1000 genomes]
rs519126	0.88[ASN][1000 genomes]
rs521607	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs522435	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs543179	1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs55742549	0.81[ASN][1000 genomes]
rs56214461	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs573351	0.83[ASN][1000 genomes]
rs578353	0.93[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap];0.89[ASN][1000 genomes]
rs580060	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs580159	0.95[ASN][1000 genomes]
rs6662108	0.93[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.83[LWK][hapmap];0.91[MEX][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap]
rs6676685	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6685252	0.99[ASN][1000 genomes]
rs696615	0.86[GIH][hapmap]
rs696616	0.87[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.90[MEX][hapmap];0.84[ASN][1000 genomes]
rs696618	0.81[CHB][hapmap];0.88[JPT][hapmap]
rs698913	0.93[CHB][hapmap];0.94[JPT][hapmap]
rs698916	0.93[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.90[MEX][hapmap];0.86[MKK][hapmap];0.81[ASN][1000 genomes]
rs698918	0.85[ASN][1000 genomes]
rs698919	0.81[ASN][1000 genomes]
rs698921	0.86[GIH][hapmap]
rs7002	0.93[CHB][hapmap];0.94[JPT][hapmap]
rs7411534	0.88[GIH][hapmap]
rs7511649	0.93[CHB][hapmap]
rs7517441	0.93[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7523428	0.92[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs7548085	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs7554686	0.93[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs8006	0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs832621	0.81[ASN][1000 genomes]
rs832622	0.93[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs834225	0.86[GIH][hapmap]
rs834229	0.81[ASN][1000 genomes]
rs834230	0.81[ASN][1000 genomes]
rs834231	0.93[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];0.94[JPT][hapmap];0.86[MEX][hapmap];0.86[MKK][hapmap];0.81[ASN][1000 genomes]
rs834232	0.93[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.94[JPT][hapmap];0.85[MEX][hapmap];0.85[MKK][hapmap];0.82[ASN][1000 genomes]
rs834234	0.87[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs834236	0.81[ASN][1000 genomes]
rs834238	0.86[GIH][hapmap]
rs834241	0.81[ASN][1000 genomes]
rs834242	0.87[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs834243	0.83[ASN][1000 genomes]
rs844309	0.81[ASN][1000 genomes]
rs9435997	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9436112	0.87[JPT][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529719	chr1:150006344-150311095	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
2	nsv916014	chr1:150187139-150537483	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
3	nsv1009508	chr1:150211112-150270830	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer 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 target site	36 gene(s)	inside rSNPs	diseases
4	nsv1011223	chr1:150229205-150279380	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs7512552	TNFAIP8L2	cis	cerebellum	SCAN
rs7512552	MRPS21	cis	cerebellum	SCAN
rs7512552	MRPS21	cis	parietal	SCAN
rs7512552	SEC22B	cis	parietal	SCAN
rs7512552	ADAMTSL4	cis	parietal	SCAN
rs7512552	SNX27	cis	parietal	SCAN
rs7512552	PER3	trans	lymphoblastoid	seeQTL

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150254600-150266200	Weak transcription	Small Intestine	intestine
2	chr1:150255400-150265800	Weak transcription	HSMMtube	muscle
3	chr1:150255400-150266200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr1:150255600-150265800	Weak transcription	Aorta	Aorta
5	chr1:150255800-150266000	Weak transcription	Gastric	stomach
6	chr1:150256000-150265800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:150256000-150265800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:150256000-150266000	Weak transcription	Pancreas	Pancrea
9	chr1:150256200-150265800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:150256200-150265800	Weak transcription	Fetal Intestine Small	intestine
11	chr1:150256200-150265800	Weak transcription	HMEC	breast
12	chr1:150256200-150266000	Weak transcription	Lung	lung
13	chr1:150256200-150266000	Weak transcription	Spleen	Spleen
14	chr1:150258400-150266000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:150259400-150265800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr1:150259400-150265800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:150259400-150265800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:150259400-150265800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:150259400-150266000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr1:150259400-150266000	Weak transcription	Esophagus	oesophagus
21	chr1:150259800-150265800	Weak transcription	Ovary	ovary
22	chr1:150260000-150265800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:150260200-150265800	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr1:150260400-150265800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr1:150265000-150265800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr1:150265200-150265800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr1:150265200-150265800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr1:150265400-150265800	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr1:150265400-150265800	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr1:150265400-150265800	Enhancers	Primary B cells from peripheral blood	blood
31	chr1:150265400-150265800	Enhancers	Primary T cells fromperipheralblood	blood
32	chr1:150265400-150265800	Enhancers	Primary hematopoietic stem cells	blood
33	chr1:150265400-150265800	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr1:150265400-150265800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr1:150265400-150265800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr1:150265400-150265800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr1:150265400-150265800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:150265400-150265800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr1:150265400-150265800	Enhancers	Adipose Nuclei	Adipose
40	chr1:150265400-150265800	Flanking Active TSS	Brain Anterior Caudate	brain
41	chr1:150265400-150265800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
42	chr1:150265400-150265800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:150265400-150265800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr1:150265400-150265800	Enhancers	Fetal Heart	heart
45	chr1:150265400-150265800	Enhancers	Fetal Intestine Large	intestine
46	chr1:150265400-150265800	Flanking Active TSS	Fetal Lung	lung
47	chr1:150265400-150265800	Enhancers	Fetal Muscle Trunk	muscle
48	chr1:150265400-150265800	Enhancers	Fetal Muscle Leg	muscle
49	chr1:150265400-150265800	Enhancers	Fetal Stomach	stomach
50	chr1:150265400-150265800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle

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