Variant report

Variant	rs1849740
Chromosome Location	chr17:33760302-33760303
allele	A/G
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	YY1	chr17:33760254-33760696	H1-hESC	embryonic stem cell:	n/a	n/a
2	JUND	chr17:33760174-33760980	H1-hESC	embryonic stem cell:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781 chr17:33760772-33760783
3	MAX	chr17:33760143-33761011	SK-N-SH	brain:	n/a	chr17:33760774-33760783 chr17:33760773-33760782
4	JUND	chr17:33759460-33761054	H1-hESC	embryonic stem cell:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781 chr17:33760772-33760783
5	FOSL1	chr17:33760265-33760510	H1-hESC	embryonic stem cell:	n/a	chr17:33760392-33760404 chr17:33760393-33760403 chr17:33760394-33760402 chr17:33760395-33760406
6	HDAC2	chr17:33760136-33760999	H1-hESC	embryonic stem cell:	n/a	chr17:33760946-33760960
7	POLR2A	chr17:33759125-33760641	U87	brain:	n/a	n/a
8	TEAD4	chr17:33760088-33761100	SK-N-SH	brain:	n/a	n/a
9	BACH1	chr17:33759792-33760985	H1-hESC	embryonic stem cell:	n/a	chr17:33760771-33760785
10	CHD2	chr17:33760242-33761030	H1-hESC	embryonic stem cell:	n/a	chr17:33760315-33760322
11	SP1	chr17:33760077-33761012	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr17:33759182-33760605	IMR90	lung:	n/a	n/a
13	CTCF	chr17:33760280-33760430	GM06990	blood:	n/a	n/a
14	POLR2A	chr17:33759177-33761080	HUVEC	blood vessel:	n/a	n/a
15	NFIC	chr17:33759550-33760323	GM12878	blood:	n/a	n/a
16	CTCF	chr17:33760240-33760390	HCM	heart:	n/a	n/a
17	NFIC	chr17:33760130-33761120	SK-N-SH	brain:	n/a	n/a
18	POLR2A	chr17:33759218-33760610	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr17:33759331-33760969	U87	brain:	n/a	n/a
20	JUND	chr17:33760027-33761125	SK-N-SH	brain:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781 chr17:33760772-33760783
21	SIN3AK20	chr17:33760279-33760906	SK-N-SH	brain:	n/a	n/a
22	POLR2A	chr17:33759327-33760902	GM12878	blood:	n/a	n/a
23	POLR2A	chr17:33760129-33760610	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr17:33759163-33760700	GM12892	blood:	n/a	n/a
25	FOSL2	chr17:33760180-33761019	SK-N-SH	brain:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760771-33760782 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781
26	MYC	chr17:33760047-33760984	NB4	blood:	n/a	chr17:33760774-33760783 chr17:33760773-33760782
27	MYC	chr17:33759990-33760899	H1-hESC	embryonic stem cell:	n/a	chr17:33760774-33760783 chr17:33760773-33760782
28	PML	chr17:33759036-33760931	GM12878	blood:	n/a	chr17:33759774-33759782 chr17:33760775-33760784 chr17:33760772-33760781
29	YY1	chr17:33760114-33760725	H1-hESC	embryonic stem cell:	n/a	n/a
30	FOS	chr17:33760254-33760980	MCF10A-Er-Src	breast:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760772-33760783 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781
31	MAFK	chr17:33760280-33760914	H1-hESC	embryonic stem cell:	n/a	chr17:33760771-33760785 chr17:33760772-33760781 chr17:33760775-33760784 chr17:33760770-33760786 chr17:33760774-33760784
32	POLR2A	chr17:33759277-33761164	PANC-1	pancreas:	n/a	n/a
33	POLR2A	chr17:33758696-33760704	H1-hESC	embryonic stem cell:	n/a	n/a
34	TCF7L2	chr17:33760139-33760960	PANC-1	pancreas:	n/a	chr17:33760773-33760782 chr17:33760774-33760783
35	MAX	chr17:33760103-33760336	GM12878	blood:	n/a	n/a
36	TCF7L2	chr17:33760158-33761035	HCT-116	colon:	n/a	chr17:33760773-33760782 chr17:33760774-33760783
37	TEAD4	chr17:33760198-33761079	HCT-116	colon:	n/a	n/a
38	CEBPB	chr17:33760241-33760955	IMR90	lung:	n/a	n/a
39	CTCF	chr17:33760300-33760450	GM12866	blood:	n/a	n/a
40	JUND	chr17:33760061-33761112	SK-N-SH	brain:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781 chr17:33760772-33760783
41	POLR2A	chr17:33759169-33760990	GM12891	blood:	n/a	n/a
42	ATF2	chr17:33760159-33760921	H1-hESC	embryonic stem cell:	n/a	n/a
43	SPI1	chr17:33760109-33760407	GM12891	blood:	n/a	n/a
44	FOS	chr17:33759472-33761028	HUVEC	blood vessel:	n/a	chr17:33760392-33760404 chr17:33760774-33760782 chr17:33760772-33760784 chr17:33760393-33760403 chr17:33760772-33760783 chr17:33760773-33760782 chr17:33760394-33760402 chr17:33760773-33760783 chr17:33760774-33760783 chr17:33760395-33760406 chr17:33760774-33760781
45	ATF3	chr17:33760267-33760589	H1-hESC	embryonic stem cell:	n/a	n/a
46	TCF12	chr17:33760215-33760550	H1-hESC	embryonic stem cell:	n/a	chr17:33760271-33760278 chr17:33760267-33760277
47	TEAD4	chr17:33760152-33761061	A549	lung:	n/a	n/a
48	POLR2A	chr17:33759238-33761150	PANC-1	pancreas:	n/a	n/a
49	EP300	chr17:33760040-33761163	SK-N-SH	brain:	n/a	chr17:33760282-33760289 chr17:33760774-33760783 chr17:33760773-33760782
50	CTCF	chr17:33760160-33760310	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33760293-33760343	PFSK-1	brain:	n/a
2	chr17:33760293-33760343	AG10803	skin:	n/a
3	chr17:33760293-33760343	HRCEpiC	kidney:	n/a
4	chr17:33760293-33760343	CMK	blood:	n/a
5	chr17:33760293-33760343	HCM	heart:	n/a
6	chr17:33760293-33760343	HRE	kidney:	n/a
7	chr17:33760293-33760343	IMR90	lung:	fetal
8	chr17:33760293-33760343	BJ	skin:	n/a
9	chr17:33760293-33760343	HNPCEpiC	eye:	n/a
10	chr17:33760293-33760343	SK-N-SH	brain:	n/a
11	chr17:33760293-33760343	Caco-2	colon:	n/a
12	chr17:33760293-33760343	U87	brain:	n/a
13	chr17:33760293-33760343	HMEC	breast:	n/a
14	chr17:33760293-33760343	Hepatocyte	liver:	n/a
15	chr17:33760293-33760343	GM12891	blood:	n/a
16	chr17:33760293-33760343	NHBE	bronchial:	n/a
17	chr17:33760293-33760343	GM12878	blood:	n/a
18	chr17:33760293-33760343	HPAEpiC	pulmonary alveolar:	n/a
19	chr17:33760293-33760343	HEEpiC	esophagus:	n/a
20	chr17:33760293-33760343	MCF10A-Er-Src	breast:	n/a
21	chr17:33760293-33760343	HUVEC	blood vessel:	n/a
22	chr17:33760293-33760343	H1-hESC	embryonic stem cell:	embryo
23	chr17:33760293-33760343	HCPEpiC	choroid plexus:	n/a
24	chr17:33760293-33760343	HEK293	kidney:	embryo
25	chr17:33760293-33760343	HCF	heart:	n/a
26	chr17:33760293-33760343	AG09319	gingival:	n/a
27	chr17:33760293-33760343	Hela-S3	cervix:	n/a
28	chr17:33760293-33760343	HL-60	blood:	n/a
29	chr17:33760293-33760343	RPTEC	kidney:	n/a
30	chr17:33760293-33760343	SK-N-SH_RA	brain:	n/a
31	chr17:33760293-33760343	PrEC	prostate:	n/a
32	chr17:33760293-33760343	K562	blood:	n/a
33	chr17:33760293-33760343	MCF-7	breast:	n/a
34	chr17:33760293-33760343	HAEpiC	amniotic membrane:	n/a
35	chr17:33760293-33760343	AG04449	skin:	fetal
36	chr17:33760293-33760343	ProgFib	skin:	n/a
37	chr17:33760293-33760343	ECC-1	luminal epithelium:	n/a
38	chr17:33760293-33760343	LNCaP	prostate:	n/a
39	chr17:33760293-33760343	HIPEpiC	eye:	n/a
40	chr17:33760293-33760343	HCT-116	colon:	n/a
41	chr17:33760293-33760343	Jurkat	blood:	n/a
42	chr17:33760293-33760343	PANC-1	pancreas:	n/a
43	chr17:33760293-33760343	SKMC	muscle:	n/a
44	chr17:33760293-33760343	AoSMC	blood vessel:	n/a
45	chr17:33760293-33760343	GM06990	blood:	n/a
46	chr17:33760293-33760343	GM19239	blood:	n/a
47	chr17:33760293-33760343	SAEC	small airway:	n/a
48	chr17:33760293-33760343	HRPEpiC	eye:	n/a
49	chr17:33760293-33760343	NH-A	brain:	n/a
50	chr17:33760293-33760343	T-47D	breast:	n/a

Variant related genes	Relation type
SLFN12	TF binding region
SLFN12	CpG island

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs1060879	0.84[AFR][1000 genomes]
rs7213069	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055936	chr17:33327166-33884184	Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer 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	112 gene(s)	inside rSNPs	diseases
2	nsv543317	chr17:33327166-33884184	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers 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	112 gene(s)	inside rSNPs	diseases
3	nsv534371	chr17:33456878-34094068	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv574741	chr17:33552275-33827134	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
5	nsv457725	chr17:33664044-33774159	Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv574743	chr17:33664044-33774159	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv515566	chr17:33664818-33768199	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv1064831	chr17:33676494-33768199	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	esv2762399	chr17:33676506-33768199	Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv908077	chr17:33677495-33763678	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv908078	chr17:33677495-33769862	ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv869869	chr17:33677545-33773100	Strong transcription Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	esv3346898	chr17:33680445-33768671	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
14	nsv574746	chr17:33684035-33762317	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
15	nsv457726	chr17:33684035-33763678	Bivalent/Poised TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
16	nsv574747	chr17:33684035-33763678	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
17	nsv457727	chr17:33684035-33766947	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
18	nsv574748	chr17:33684035-33766947	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
19	nsv457728	chr17:33684035-33768199	Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
20	nsv574749	chr17:33684035-33768199	Enhancers Genic enhancers Strong transcription Weak 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	10 gene(s)	inside rSNPs	diseases
21	nsv457730	chr17:33684107-33763678	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
22	nsv574750	chr17:33684107-33763678	Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
23	nsv1056952	chr17:33684107-33766206	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
24	nsv1055525	chr17:33684107-33768199	Enhancers Genic enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
25	nsv1067402	chr17:33684107-33769206	Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
26	nsv1056116	chr17:33691457-33815452	Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
27	esv3432530	chr17:33738621-33802241	Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33749200-33761000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr17:33757400-33760800	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr17:33757800-33760400	Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr17:33757800-33760400	Active TSS	NHLF	lung
5	chr17:33758200-33760400	Active TSS	HSMM	muscle
6	chr17:33758200-33761000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr17:33758400-33760400	Active TSS	Fetal Kidney	kidney
8	chr17:33758400-33760400	Active TSS	Fetal Lung	lung
9	chr17:33758400-33760600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr17:33758400-33760800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr17:33758600-33760400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr17:33758600-33760400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr17:33758600-33760400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
14	chr17:33758600-33760400	Active TSS	Rectal Smooth Muscle	rectum
15	chr17:33758600-33761000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr17:33758600-33761000	Active TSS	Aorta	Aorta
17	chr17:33758600-33761200	Flanking Active TSS	Adipose Nuclei	Adipose
18	chr17:33758800-33760400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr17:33758800-33760800	Active TSS	H9 Cell Line	embryonic stem cell
20	chr17:33758800-33760800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr17:33758800-33760800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr17:33758800-33760800	Active TSS	Colonic Mucosa	Colon
23	chr17:33759000-33760400	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr17:33759000-33760400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr17:33759000-33760400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr17:33759000-33760400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
27	chr17:33759000-33760400	Active TSS	Brain Substantia Nigra	brain
28	chr17:33759000-33760400	Active TSS	Duodenum Smooth Muscle	Duodenum
29	chr17:33759000-33760400	Active TSS	Rectal Mucosa Donor 31	rectum
30	chr17:33759000-33760400	Active TSS	Stomach Mucosa	stomach
31	chr17:33759000-33760400	Active TSS	Osteobl	bone
32	chr17:33759000-33760600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
33	chr17:33759000-33760600	Active TSS	Thymus	Thymus
34	chr17:33759200-33760400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr17:33759200-33760400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr17:33759200-33760400	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr17:33759200-33760400	Active TSS	Esophagus	oesophagus
38	chr17:33759200-33760400	Bivalent/Poised TSS	Fetal Brain Female	brain
39	chr17:33759200-33760400	Active TSS	Left Ventricle	heart
40	chr17:33759200-33760600	Active TSS	Colon Smooth Muscle	Colon
41	chr17:33759200-33761000	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr17:33759200-33761000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr17:33759200-33761000	Active TSS	Rectal Mucosa Donor 29	rectum
44	chr17:33759200-33761000	Active TSS	Right Atrium	heart
45	chr17:33759200-33761200	Active TSS	Ovary	ovary
46	chr17:33759400-33760400	Active TSS	H1 Cell Line	embryonic stem cell
47	chr17:33759400-33760400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
48	chr17:33759400-33760400	Active TSS	Duodenum Mucosa	Duodenum
49	chr17:33759400-33760400	Active TSS	Stomach Smooth Muscle	stomach
50	chr17:33759400-33760800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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