Variant report

Variant	rs649639
Chromosome Location	chr1:10490285-10490286
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	EGR1	chr1:10490088-10491191	HCT-116	colon:	n/a	chr1:10490750-10490759 chr1:10490721-10490735 chr1:10490350-10490360
2	ZNF143	chr1:10490247-10491202	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr1:10490174-10491199	GM19193	blood:	n/a	n/a
4	CTCF	chr1:10490226-10490605	ECC-1	luminal epithelium:	n/a	chr1:10490427-10490437 chr1:10490422-10490440 chr1:10490425-10490438 chr1:10490423-10490439 chr1:10490425-10490438 chr1:10490425-10490434
5	POLR2A	chr1:10490008-10491366	GM12878	blood:	n/a	n/a
6	POLR2A	chr1:10490262-10491087	HCT-116	colon:	n/a	n/a
7	CTCF	chr1:10490247-10490568	Spleen_OC	spleen:	n/a	chr1:10490427-10490437 chr1:10490422-10490440 chr1:10490425-10490438 chr1:10490423-10490439 chr1:10490425-10490438 chr1:10490425-10490434
8	CHD2	chr1:10490179-10491510	GM12878	blood:	n/a	n/a
9	POLR2A	chr1:10490088-10491011	K562	blood:	n/a	n/a
10	JUND	chr1:10490031-10491147	K562	blood:	n/a	n/a
11	CTCF	chr1:10490280-10490563	K562	blood:	n/a	chr1:10490427-10490437 chr1:10490422-10490440 chr1:10490425-10490438 chr1:10490423-10490439 chr1:10490425-10490438 chr1:10490425-10490434
12	POLR2A	chr1:10490251-10491230	U87	brain:	n/a	n/a
13	UBTF	chr1:10490195-10491528	K562	blood:	n/a	n/a
14	CHD2	chr1:10490257-10490930	K562	blood:	n/a	n/a
15	FOXM1	chr1:10490105-10491180	GM12878	blood:	n/a	n/a
16	RFX5	chr1:10490279-10490903	K562	blood:	n/a	chr1:10490792-10490807 chr1:10490792-10490807 chr1:10490792-10490807
17	TCF12	chr1:10490139-10491395	ECC-1	luminal epithelium:	n/a	n/a
18	EGR1	chr1:10490164-10490899	K562	blood:	n/a	chr1:10490750-10490759 chr1:10490721-10490735 chr1:10490350-10490360
19	CTCF	chr1:10490207-10490568	A549	lung:	n/a	chr1:10490427-10490437 chr1:10490422-10490440 chr1:10490425-10490438 chr1:10490423-10490439 chr1:10490425-10490438 chr1:10490425-10490434
20	MAX	chr1:10489978-10491108	HUVEC	blood vessel:	n/a	chr1:10490255-10490262
21	TBL1XR1	chr1:10490105-10491547	K562	blood:	n/a	n/a
22	YY1	chr1:10490226-10491017	K562	blood:	n/a	chr1:10490696-10490710 chr1:10490821-10490835 chr1:10490692-10490703
23	POLR2A	chr1:10490001-10491062	GM12891	blood:	n/a	n/a
24	ZBTB7A	chr1:10490131-10491135	ECC-1	luminal epithelium:	n/a	chr1:10490528-10490535 chr1:10490430-10490439
25	SIN3AK20	chr1:10490052-10491405	PANC-1	pancreas:	n/a	n/a
26	EP300	chr1:10490096-10490461	K562	blood:	n/a	n/a
27	POLR2A	chr1:10490232-10491258	HEK293	kidney:	n/a	n/a
28	POLR2A	chr1:10490088-10491133	PANC-1	pancreas:	n/a	n/a
29	SIN3AK20	chr1:10490266-10490572	A549	lung:	n/a	n/a
30	KAP1	chr1:10490063-10490709	HEK293	kidney:	n/a	n/a
31	MAX	chr1:10490265-10491360	Hela-S3	cervix:	n/a	n/a
32	ZBTB33	chr1:10490273-10490606	GM12878	blood:	n/a	n/a
33	ATF2	chr1:10490155-10491320	H1-hESC	embryonic stem cell:	n/a	n/a
34	HEY1	chr1:10490148-10491053	K562	blood:	n/a	n/a
35	CTCF	chr1:10490239-10490588	GM12891	blood:	n/a	chr1:10490427-10490437 chr1:10490422-10490440 chr1:10490425-10490438 chr1:10490423-10490439 chr1:10490425-10490438 chr1:10490425-10490434
36	ATF2	chr1:10490050-10491090	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr1:10490130-10491094	GM12878	blood:	n/a	n/a
38	RAD21	chr1:10490227-10490577	K562	blood:	n/a	chr1:10490428-10490438 chr1:10490378-10490388 chr1:10490423-10490442
39	E2F6	chr1:10490253-10491133	K562	blood:	n/a	chr1:10490750-10490759 chr1:10490696-10490706 chr1:10490431-10490440 chr1:10490495-10490506
40	CHD1	chr1:10490254-10491126	GM12878	blood:	n/a	n/a
41	POLR2A	chr1:10490195-10491350	Hela-S3	cervix:	n/a	n/a
42	ELK1	chr1:10490257-10491041	GM12878	blood:	n/a	n/a
43	MYC	chr1:10490137-10491213	K562	blood:	n/a	chr1:10490255-10490262
44	RAD21	chr1:10490243-10490587	A549	lung:	n/a	chr1:10490428-10490438 chr1:10490378-10490388 chr1:10490423-10490442
45	CTCF	chr1:10490237-10490529	A549	lung:	n/a	chr1:10490427-10490437 chr1:10490422-10490440 chr1:10490425-10490438 chr1:10490423-10490439 chr1:10490425-10490438 chr1:10490425-10490434
46	ZBTB33	chr1:10490254-10490581	GM12878	blood:	n/a	n/a
47	ELF1	chr1:10490241-10491013	K562	blood:	n/a	n/a
48	RAD21	chr1:10490224-10490579	GM12878	blood:	n/a	chr1:10490428-10490438 chr1:10490378-10490388 chr1:10490423-10490442
49	FOXM1	chr1:10490162-10491077	GM12878	blood:	n/a	n/a
50	E2F4	chr1:10490213-10491409	K562	blood:	n/a	chr1:10490750-10490759 chr1:10490696-10490706 chr1:10490431-10490440 chr1:10490495-10490506

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10490236-10490286	GM06990	blood:	n/a
2	chr1:10490236-10490286	HCT-116	colon:	n/a
3	chr1:10490236-10490286	HIPEpiC	eye:	n/a
4	chr1:10490236-10490286	NB4	blood:	n/a
5	chr1:10490236-10490286	IMR90	lung:	fetal
6	chr1:10490236-10490286	HRCEpiC	kidney:	n/a
7	chr1:10490236-10490286	NHDF-neo	bronchial:	n/a
8	chr1:10490236-10490286	GM12891	blood:	n/a
9	chr1:10490236-10490286	GM19239	blood:	n/a
10	chr1:10490236-10490286	BJ	skin:	n/a
11	chr1:10490236-10490286	HCM	heart:	n/a
12	chr1:10490236-10490286	MCF-7	breast:	n/a
13	chr1:10490236-10490286	HRE	kidney:	n/a
14	chr1:10490236-10490286	PANC-1	pancreas:	n/a
15	chr1:10490236-10490286	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:10490236-10490286	HEEpiC	esophagus:	n/a
17	chr1:10490236-10490286	HepG2	liver:	n/a
18	chr1:10490236-10490286	HCPEpiC	choroid plexus:	n/a
19	chr1:10490236-10490286	Hela-S3	cervix:	n/a
20	chr1:10490236-10490286	PrEC	prostate:	n/a
21	chr1:10490236-10490286	LNCaP	prostate:	n/a
22	chr1:10490236-10490286	SK-N-SH	brain:	n/a
23	chr1:10490236-10490286	Hepatocyte	liver:	n/a
24	chr1:10490236-10490286	PFSK-1	brain:	n/a
25	chr1:10490236-10490286	ProgFib	skin:	n/a
26	chr1:10490236-10490286	Jurkat	blood:	n/a
27	chr1:10490236-10490286	K562	blood:	n/a
28	chr1:10490236-10490286	HRPEpiC	eye:	n/a
29	chr1:10490236-10490286	AG10803	skin:	n/a
30	chr1:10490236-10490286	T-47D	breast:	n/a
31	chr1:10490236-10490286	ECC-1	luminal epithelium:	n/a
32	chr1:10490236-10490286	SKMC	muscle:	n/a
33	chr1:10490236-10490286	SAEC	small airway:	n/a
34	chr1:10490236-10490286	A549	lung:	n/a
35	chr1:10490236-10490286	U87	brain:	n/a
36	chr1:10490236-10490286	HCF	heart:	n/a
37	chr1:10490236-10490286	ovcar-3	ovarian:	n/a
38	chr1:10490236-10490286	AG04449	skin:	fetal
39	chr1:10490236-10490286	AoSMC	blood vessel:	n/a
40	chr1:10490236-10490286	AG09309	skin:	n/a
41	chr1:10490236-10490286	H1-hESC	embryonic stem cell:	embryo
42	chr1:10490236-10490286	BE2_C	brain:	n/a
43	chr1:10490236-10490286	HL-60	blood:	n/a
44	chr1:10490236-10490286	AG09319	gingival:	n/a
45	chr1:10490236-10490286	MCF10A-Er-Src	breast:	n/a
46	chr1:10490236-10490286	HNPCEpiC	eye:	n/a
47	chr1:10490236-10490286	NH-A	brain:	n/a
48	chr1:10490236-10490286	HMEC	breast:	n/a
49	chr1:10490236-10490286	HUVEC	blood vessel:	n/a
50	chr1:10490236-10490286	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:10475041..10475642-chr1:10489986..10490702,2	K562	blood:
2	chr1:10270585..10272249-chr1:10490197..10491890,2	K562	blood:
3	chr1:10490187..10490687-chr12:52449617..52450158,2	Hela-S3	cervix:
4	chr1:10457794..10460664-chr1:10487844..10492697,5	K562	blood:
5	chr1:10488008..10492443-chr1:10531123..10534892,8	K562	blood:
6	chr1:10490085..10492364-chr1:10508772..10511442,3	K562	blood:
7	chr1:10488905..10491611-chr1:10518532..10520834,2	MCF-7	breast:
8	chr1:10489993..10493018-chr1:10531254..10535234,5	MCF-7	breast:
9	chr1:10489448..10493967-chr1:10494423..10498103,7	K562	blood:
10	chr1:10457794..10461321-chr1:10487053..10491931,7	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DFFA-1	chr1:10489938-10490734	ENSG00000271989.1

Variant related genes	Relation type
APITD1	TF binding region
APITD1-CORT	TF binding region
APITD1-CORT	CpG island
APITD1	CpG island
ENSG00000123358	Chromatin interaction
ENSG00000160049	Chromatin interaction
ENSG00000142657	Chromatin interaction
ENSG00000054523	Chromatin interaction
ENSG00000142655	Chromatin interaction
ENSG00000241563	Chromatin interaction
ENSG00000251503	Chromatin interaction
ENSG00000203469	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10746494	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1203122	0.87[EUR][1000 genomes]
rs1307485	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1307487	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1750349	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1760664	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2483684	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2781233	0.86[EUR][1000 genomes]
rs36013615	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs475549	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs481571	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs491880	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs505141	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs517241	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs519472	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs520964	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs522029	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs522280	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs524150	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs528713	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs579398	0.93[ASN][1000 genomes]
rs583515	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs585703	0.96[ASN][1000 genomes]
rs586096	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs586223	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs597441	0.85[EUR][1000 genomes]
rs628462	0.81[ASN][1000 genomes]
rs632690	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs634358	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs643400	0.89[EUR][1000 genomes]
rs649101	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs655271	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs666583	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs667366	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs672606	0.86[EUR][1000 genomes]
rs678850	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs681448	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs681495	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757722	chr1:10238070-10582554	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv2758920	chr1:10238070-10582554	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv817370	chr1:10305470-10697150	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1008021	chr1:10363794-10802633	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv2764192	chr1:10383734-10594186	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv1003498	chr1:10445928-10607351	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv998731	chr1:10464176-10607351	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	esv3373675	chr1:10489565-10491863	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10480200-10490400	Weak transcription	Aorta	Aorta
2	chr1:10489800-10490400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr1:10489800-10490400	Flanking Active TSS	Primary T cells from cord blood	blood
4	chr1:10489800-10490400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr1:10489800-10490400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:10489800-10490400	Flanking Active TSS	Adipose Nuclei	Adipose
7	chr1:10489800-10490400	Flanking Active TSS	Brain Hippocampus Middle	brain
8	chr1:10489800-10490400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
9	chr1:10489800-10490400	Enhancers	Lung	lung
10	chr1:10489800-10490400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
11	chr1:10489800-10490400	Flanking Active TSS	Dnd41	blood
12	chr1:10489800-10490400	Flanking Active TSS	GM12878-XiMat	blood
13	chr1:10489800-10490400	Flanking Active TSS	Hela-S3	cervix
14	chr1:10489800-10490400	Flanking Active TSS	K562	blood
15	chr1:10489800-10491400	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr1:10489800-10491400	Active TSS	Brain Germinal Matrix	brain
17	chr1:10489800-10491600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr1:10489800-10491600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr1:10490000-10490400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
20	chr1:10490000-10490400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:10490000-10490400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:10490000-10490400	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:10490000-10490400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr1:10490000-10490400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:10490000-10490400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:10490000-10490400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr1:10490000-10490400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr1:10490000-10490400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
29	chr1:10490000-10490400	Flanking Active TSS	Primary B cells from peripheral blood	blood
30	chr1:10490000-10490400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
31	chr1:10490000-10490400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr1:10490000-10490400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr1:10490000-10490400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
34	chr1:10490000-10490400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
35	chr1:10490000-10490400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
36	chr1:10490000-10490400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
37	chr1:10490000-10490400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr1:10490000-10490400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr1:10490000-10490400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
40	chr1:10490000-10490400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
41	chr1:10490000-10490400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr1:10490000-10490400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr1:10490000-10490400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:10490000-10490400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr1:10490000-10490400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
46	chr1:10490000-10490400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:10490000-10490400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:10490000-10490400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:10490000-10490400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:10490000-10490400	Flanking Active TSS	Liver	Liver

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