Variant report

Variant	rs2575695
Chromosome Location	chr8:104385716-104385717
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	CTCF	chr8:104385507-104385734	MCF-7	breast:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
2	CTCF	chr8:104385515-104385730	A549	lung:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
3	CTCF	chr8:104385449-104385744	SK-N-SH_RA	brain:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
4	RAD21	chr8:104383970-104385893	HCT-116	colon:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
5	CTCF	chr8:104385507-104385756	Kidney_OC	kidney:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
6	SIN3AK20	chr8:104385341-104385838	SK-N-SH	brain:	n/a	n/a
7	RAD21	chr8:104385372-104385747	SK-N-SH_RA	brain:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
8	CTCF	chr8:104385506-104385746	LNCaP	prostate:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
9	MAX	chr8:104383301-104385874	HCT-116	colon:	n/a	chr8:104383634-104383644 chr8:104383467-104383476 chr8:104383465-104383473 chr8:104383661-104383670 chr8:104383466-104383477 chr8:104383465-104383478
10	CTCF	chr8:104385600-104385750	HAc	cerebellar:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
11	CTCF	chr8:104385501-104385742	GM13977	blood:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
12	CTCF	chr8:104385455-104385824	K562	blood:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
13	CTCF	chr8:104385400-104385757	ECC-1	luminal epithelium:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
14	CTCF	chr8:104385300-104385974	MCF-7	breast:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
15	JUND	chr8:104385496-104385776	K562	blood:	n/a	n/a
16	RAD21	chr8:104385370-104385821	H1-hESC	embryonic stem cell:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
17	CTCF	chr8:104385509-104385739	ProgFib	skin:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
18	SMC3	chr8:104383479-104386604	SK-N-SH	brain:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104384498-104384505 chr8:104385618-104385625
19	RAD21	chr8:104385329-104385785	HepG2	liver:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
20	ZNF384	chr8:104385419-104385959	K562	blood:	n/a	n/a
21	CTCF	chr8:104385480-104385755	ECC-1	luminal epithelium:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
22	BHLHE40	chr8:104385449-104385727	K562	blood:	n/a	n/a
23	CTCF	chr8:104385420-104385804	A549	lung:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
24	CTCF	chr8:104385252-104385898	GM12878	blood:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
25	RAD21	chr8:104385306-104385895	A549	lung:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
26	CTCF	chr8:104385474-104385719	HepG2	liver:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
27	TAF1	chr8:104385488-104385814	PFSK-1	brain:	n/a	n/a
28	CTCF	chr8:104385509-104385727	GM19240	blood:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
29	CTCF	chr8:104385180-104386093	HCT-116	colon:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
30	MAZ	chr8:104385435-104385867	K562	blood:	n/a	n/a
31	YY1	chr8:104385391-104385969	SK-N-SH	brain:	n/a	n/a
32	GATA3	chr8:104384069-104386185	SK-N-SH	brain:	n/a	chr8:104384574-104384583
33	CTCF	chr8:104385580-104385730	HCFaa	heart:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
34	RAD21	chr8:104385426-104385795	Hela-S3	cervix:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
35	RAD21	chr8:104385294-104385857	MCF-7	breast:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
36	ZMIZ1	chr8:104385384-104385738	K562	blood:	n/a	n/a
37	E2F4	chr8:104385469-104385925	MCF10A-Er-Src	breast:	n/a	n/a
38	CTCF	chr8:104385345-104385914	MCF-7	breast:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
39	RAD21	chr8:104385332-104385846	SK-N-SH_RA	brain:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
40	CTCF	chr8:104385580-104385730	HL-60	blood:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
41	CTCF	chr8:104385357-104385770	T-47D	breast:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
42	POLR2A	chr8:104383590-104386072	IMR90	lung:	n/a	n/a
43	CTCF	chr8:104385516-104385730	A549	lung:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
44	EBF1	chr8:104385332-104385793	GM12878	blood:	n/a	n/a
45	RAD21	chr8:104385381-104385870	A549	lung:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
46	CTCF	chr8:104385507-104385749	LNCaP	prostate:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
47	UBTF	chr8:104385583-104385783	K562	blood:	n/a	n/a
48	RAD21	chr8:104385436-104385749	HepG2	liver:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623
49	CTCF	chr8:104385255-104385895	HCT-116	colon:	n/a	chr8:104385609-104385627 chr8:104385615-104385624 chr8:104385612-104385622 chr8:104385604-104385625 chr8:104385611-104385624 chr8:104385610-104385626
50	RAD21	chr8:104384302-104386039	SK-N-SH	brain:	n/a	chr8:104385611-104385621 chr8:104385611-104385625 chr8:104385609-104385621 chr8:104385607-104385626 chr8:104385610-104385623

No.	Distal block	Cell Line	Cell type
1	chr8:104385211..104386060-chr8:104524184..104524830,3	MCF-7	breast:
2	chr8:104384537..104387363-chr8:104425771..104427328,2	MCF-7	breast:
3	chr8:104289531..104293502-chr8:104385386..104388063,3	MCF-7	breast:
4	chr8:104309661..104313454-chr8:104382208..104385836,8	MCF-7	breast:
5	chr8:104383486..104387596-chr8:104393672..104397600,4	K562	blood:
6	chr8:104385225..104386793-chr8:104395425..104397023,2	K562	blood:
7	chr8:104385308..104386074-chr8:104524168..104524884,4	MCF-7	breast:
8	chr8:104164158..104164912-chr8:104385376..104386427,3	MCF-7	breast:
9	chr8:104085848..104086666-chr8:104385139..104385962,4	MCF-7	breast:
10	chr8:104384521..104386453-chr8:104425627..104427344,2	K562	blood:
11	chr8:104309966..104312210-chr8:104383451..104386900,3	MCF-7	breast:
12	chr8:104157676..104158176-chr8:104385392..104385908,2	MCF-7	breast:
13	chr8:104116271..104117073-chr8:104385047..104386147,6	MCF-7	breast:
14	chr8:104291177..104292455-chr8:104385073..104386105,8	MCF-7	breast:
15	chr8:104313517..104316996-chr8:104385407..104388642,4	MCF-7	breast:
16	chr8:104085750..104086680-chr8:104384771..104385796,4	K562	blood:
17	chr8:104382288..104384118-chr8:104384150..104386828,2	MCF-7	breast:
18	chr8:104384840..104386401-chr8:104401334..104403233,2	K562	blood:
19	chr8:104351789..104352565-chr8:104385299..104386093,2	MCF-7	breast:
20	chr8:104384672..104387548-chr8:104409163..104411650,2	K562	blood:
21	chr8:104384922..104387635-chr8:104403443..104406734,3	MCF-7	breast:

Variant related genes	Relation type
CTHRC1	TF binding region
ENSG00000164933	Chromatin interaction
ENSG00000247081	Chromatin interaction
ENSG00000164934	Chromatin interaction
ENSG00000207399	Chromatin interaction
ENSG00000266289	Chromatin interaction
ENSG00000164930	Chromatin interaction
ENSG00000164932	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs2575690	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2575700	0.81[CEU][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2687358	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2687360	0.81[CEU][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3098228	0.82[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs3098229	1.00[CHB][hapmap];0.92[JPT][hapmap];0.90[YRI][hapmap];0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs3098230	0.90[YRI][hapmap];0.81[AFR][1000 genomes]
rs3098232	0.82[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs3098246	0.87[ASN][1000 genomes]
rs3098247	0.87[ASN][1000 genomes]
rs3098254	0.82[CHB][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs3133800	0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs3133801	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3133803	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3133810	0.82[CHB][hapmap];0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs719841	0.90[YRI][hapmap]
rs827576	0.81[AMR][1000 genomes]
rs827593	0.81[AMR][1000 genomes]
rs827596	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs827598	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription 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	42 gene(s)	inside rSNPs	diseases
3	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1016395	chr8:104327541-104473005	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1023048	chr8:104355188-104872701	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv539705	chr8:104355188-104872701	ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv1021345	chr8:104361854-104879684	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
8	nsv1032085	chr8:104362187-104878345	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers 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	nsv1033477	chr8:104369940-104439632	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh 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
10	nsv539706	chr8:104369940-104439632	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh 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
11	nsv1034183	chr8:104369940-104814008	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
12	nsv539707	chr8:104369940-104814008	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2575695	DCAF13	cis	Muscle Skeletal	GTEx

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104383400-104386400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:104383400-104386600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr8:104384000-104386000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
4	chr8:104384000-104386000	Flanking Active TSS	Osteobl	bone
5	chr8:104384200-104385800	Enhancers	Brain Cingulate Gyrus	brain
6	chr8:104384200-104386400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:104384200-104394800	Weak transcription	GM12878-XiMat	blood
8	chr8:104384200-104399800	Weak transcription	Primary T cells from cord blood	blood
9	chr8:104384400-104388000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr8:104384400-104388000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:104384400-104412200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr8:104384600-104386000	Flanking Active TSS	HUVEC	blood vessel
13	chr8:104384600-104409400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:104384600-104418600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:104384800-104386000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr8:104384800-104386000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr8:104384800-104387400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr8:104384800-104392600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr8:104385000-104385800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr8:104385000-104385800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:104385000-104385800	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr8:104385000-104386000	Enhancers	Fetal Muscle Leg	muscle
23	chr8:104385000-104386000	Enhancers	Placenta Amnion	Placenta Amnion
24	chr8:104385000-104386000	Enhancers	NHLF	lung
25	chr8:104385000-104387000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr8:104385000-104399000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr8:104385000-104408800	Weak transcription	Fetal Muscle Trunk	muscle
28	chr8:104385000-104415600	Weak transcription	Placenta	Placenta
29	chr8:104385200-104385800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:104385200-104386200	Enhancers	NHEK	skin
31	chr8:104385400-104385800	Enhancers	HepG2	liver
32	chr8:104385400-104386000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr8:104385400-104386000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr8:104385400-104386000	Enhancers	Dnd41	blood
35	chr8:104385400-104386000	Enhancers	HMEC	breast
36	chr8:104385400-104386000	Active TSS	HSMMtube	muscle
37	chr8:104385400-104386800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:104385400-104388400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:104385400-104400400	Weak transcription	A549	lung
40	chr8:104385600-104385800	Active TSS	HSMM	muscle
41	chr8:104385600-104385800	Active TSS	NH-A	brain
42	chr8:104385600-104385800	Enhancers	NHDF-Ad	bronchial
43	chr8:104385600-104386000	Enhancers	Aorta	Aorta
44	chr8:104385600-104386200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr8:104385600-104386800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr8:104385600-104387200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr8:104385600-104389600	Weak transcription	Fetal Brain Male	brain
48	chr8:104385600-104399200	Weak transcription	Fetal Stomach	stomach
49	chr8:104385600-104399800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:104385600-104400200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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