Variant report

Variant	rs8067264
Chromosome Location	chr17:57182793-57182794
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	STAT3	chr17:57182642-57182826	MCF10A-Er-Src	breast:	n/a	n/a
2	GATA3	chr17:57182365-57185495	MCF-7	breast:	n/a	n/a
3	NR2F2	chr17:57182379-57185442	MCF-7	breast:	n/a	n/a
4	ZNF217	chr17:57182476-57185248	MCF-7	breast:	n/a	n/a
5	MAX	chr17:57182442-57185442	MCF-7	breast:	n/a	chr17:57183928-57183937 chr17:57183761-57183771
6	MXI1	chr17:57182340-57185455	SK-N-SH	brain:	n/a	chr17:57183595-57183604
7	GATA3	chr17:57182447-57185433	MCF-7	breast:	n/a	n/a

No data

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:57182714..57184339-chr20:55840457..55843240,2	MCF-7	breast:
2	chr17:56594256..56597406-chr17:57182255..57186228,4	K562	blood:
3	chr17:56735072..56738484-chr17:57181626..57187465,12	MCF-7	breast:
4	chr1:28906850..28909563-chr17:57182513..57184408,2	MCF-7	breast:
5	chr17:56708039..56712144-chr17:57181830..57184716,4	MCF-7	breast:
6	chr17:57182556..57185500-chr8:117885243..117887257,2	MCF-7	breast:
7	chr17:57182746..57185047-chr17:65240971..65242827,2	MCF-7	breast:
8	chr17:56755117..56758223-chr17:57182145..57185089,4	MCF-7	breast:
9	chr17:57181740..57185864-chr17:57285843..57288823,5	K562	blood:
10	chr17:57181661..57184920-chr17:57296227..57299938,4	MCF-7	breast:
11	chr17:57095356..57201201-chr17:57905452..57953516,1644	MCF-7	breast:
12	chr17:57113105..57201250-chr17:57905452..57952793,1492	MCF-7	breast:
13	chr17:57181561..57185974-chr17:57968409..57971978,11	MCF-7	breast:
14	chr17:57182605..57184308-chr5:67510766..67513738,2	MCF-7	breast:
15	chr17:57180707..57182986-chr17:57216885..57219479,2	MCF-7	breast:
16	chr17:57181911..57183689-chr20:55840485..55842263,2	MCF-7	breast:
17	chr17:56594719..56596602-chr17:57182316..57185290,3	MCF-7	breast:
18	chr17:57182396..57186542-chr17:57229642..57234395,10	MCF-7	breast:
19	chr17:57181016..57183483-chr17:59476207..59478014,2	MCF-7	breast:
20	chr17:57182695..57184596-chr17:57962308..57965102,2	MCF-7	breast:
21	chr17:57182509..57184256-chr17:58677347..58679347,2	MCF-7	breast:
22	chr17:57182611..57184630-chr2:206948377..206949909,2	MCF-7	breast:
23	chr17:57182648..57184264-chr20:52207978..52210816,2	MCF-7	breast:
24	chr17:57181517..57184200-chr3:161086879..161089854,2	MCF-7	breast:
25	chr17:57182741..57185324-chr17:57286919..57289106,3	MCF-7	breast:
26	chr17:57182576..57184136-chr8:103818187..103820992,2	MCF-7	breast:
27	chr17:57181543..57184200-chr17:59488935..59490643,2	MCF-7	breast:
28	chr1:205090841..205092733-chr17:57181641..57184309,2	MCF-7	breast:
29	chr17:57182168..57184264-chr8:128494106..128496504,2	MCF-7	breast:
30	chr17:57181515..57184136-chr8:96145563..96147575,2	MCF-7	breast:
31	chr17:57182699..57185513-chr17:57229234..57234346,6	K562	blood:
32	chr17:56706897..56710474-chr17:57182041..57185772,3	K562	blood:
33	chr17:57180310..57187428-chr17:57229084..57235888,17	MCF-7	breast:
34	chr17:56733467..56738136-chr17:57181653..57185421,10	MCF-7	breast:
35	chr17:57182638..57185887-chr17:57231156..57234780,6	K562	blood:
36	chr1:149858122..149859753-chr17:57182597..57184215,2	MCF-7	breast:
37	chr17:57181997..57185568-chr17:58154403..58156963,4	MCF-7	breast:
38	chr17:57181395..57188655-chr17:57967866..57973406,16	MCF-7	breast:
39	chr17:56769284..56772110-chr17:57182586..57184457,2	MCF-7	breast:
40	chr17:56706387..56711193-chr17:57182654..57188385,13	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000224738	TF binding region
ENSG00000184260	Chromatin interaction
ENSG00000270264	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000121101	Chromatin interaction
ENSG00000253669	Chromatin interaction
ENSG00000227946	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000108443	Chromatin interaction
ENSG00000198265	Chromatin interaction
ENSG00000197989	Chromatin interaction
ENSG00000182628	Chromatin interaction
ENSG00000226308	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000175895	Chromatin interaction
ENSG00000117222	Chromatin interaction
ENSG00000200997	Chromatin interaction
ENSG00000187013	Chromatin interaction
ENSG00000068489	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000184678	Chromatin interaction
ENSG00000108389	Chromatin interaction
ENSG00000167447	Chromatin interaction
ENSG00000153982	Chromatin interaction
ENSG00000246228	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000196542	Chromatin interaction
ENSG00000264875	Chromatin interaction
ENSG00000164754	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000145675	Chromatin interaction
ENSG00000068097	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000171940	Chromatin interaction
ENSG00000267416	Chromatin interaction
ENSG00000170836	Chromatin interaction
ENSG00000264672	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000108384	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000108423	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10853008	0.80[CEU][hapmap]
rs11079368	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11654986	0.88[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11656413	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11658694	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11658974	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11868348	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12051897	0.82[EUR][1000 genomes]
rs12452313	0.85[CEU][hapmap];0.84[CHB][hapmap]
rs12603238	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12936058	0.96[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap]
rs12947785	0.96[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap]
rs12948746	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1588322	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs1871751	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1967415	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2055779	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs2158966	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2333410	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3826353	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4372750	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs4598970	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4932693	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56297715	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56360354	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57869245	0.84[ASN][1000 genomes]
rs58092632	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6416932	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6416933	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6503887	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap]
rs6503890	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs6503893	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6503894	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6503896	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7207693	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs7208505	0.88[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7213269	0.86[YRI][hapmap]
rs7214098	0.88[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7214335	0.91[CEU][hapmap];0.81[YRI][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7214892	0.83[EUR][1000 genomes]
rs7217845	0.86[YRI][hapmap]
rs7218105	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap]
rs72628394	0.86[ASN][1000 genomes]
rs7503190	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8069033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8071280	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap]
rs8072182	0.86[YRI][hapmap]
rs8072712	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8076121	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap]
rs8081297	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8081967	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8082544	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];0.98[ASN][1000 genomes]
rs8182277	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9303403	0.86[YRI][hapmap]
rs9892425	0.86[YRI][hapmap]
rs9898916	0.91[CEU][hapmap];0.84[CHB][hapmap];0.80[JPT][hapmap]
rs9911583	0.86[YRI][hapmap]

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	nsv908643	chr17:56803028-57249010	Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
2	nsv908644	chr17:56803028-57371432	Strong transcription Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
3	esv3335958	chr17:56849544-57385398	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
4	nsv908645	chr17:56857281-57208752	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	150 gene(s)	inside rSNPs	diseases
5	nsv1065063	chr17:56954121-57346694	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers 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 miRNA target site	227 gene(s)	inside rSNPs	diseases
6	nsv1064384	chr17:57049519-57346694	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
7	nsv908646	chr17:57061238-57255810	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	206 gene(s)	inside rSNPs	diseases
8	nsv833499	chr17:57070693-57288410	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers 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	208 gene(s)	inside rSNPs	diseases
9	nsv1066388	chr17:57082013-57339981	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	209 gene(s)	inside rSNPs	diseases
10	esv2758462	chr17:57082579-57425634	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	213 gene(s)	inside rSNPs	diseases
11	esv2758699	chr17:57082579-57425634	Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	213 gene(s)	inside rSNPs	diseases
12	nsv1066467	chr17:57117682-57338731	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases
13	nsv1057209	chr17:57117682-57742240	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised 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 miRNA target site	240 gene(s)	inside rSNPs	diseases
14	nsv543396	chr17:57117682-57742240	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	240 gene(s)	inside rSNPs	diseases
15	nsv1066788	chr17:57126446-57344129	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	193 gene(s)	inside rSNPs	diseases
16	nsv482858	chr17:57136446-57288615	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	184 gene(s)	inside rSNPs	diseases
17	nsv908647	chr17:57165097-57290383	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	173 gene(s)	inside rSNPs	diseases
18	nsv908648	chr17:57165097-57322954	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	179 gene(s)	inside rSNPs	diseases
19	nsv1063542	chr17:57179669-57569673	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
20	nsv543397	chr17:57179669-57569673	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
21	nsv1062959	chr17:57179669-57680772	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs8067264	RAD51C	Cis_1M	lymphoblastoid	RTeQTL
rs8067264	TRIM37	cis	Adipose Subcutaneous	GTEx
rs8067264	TRIM37	cis	Muscle Skeletal	GTEx
rs8067264	TRIM37	cis	Whole Blood	GTEx

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:57121400-57183400	Weak transcription	Gastric	stomach
2	chr17:57135400-57183400	Weak transcription	Pancreas	Pancrea
3	chr17:57137600-57183000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr17:57167400-57183000	Weak transcription	Brain Substantia Nigra	brain
5	chr17:57167400-57183000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr17:57167400-57183400	Weak transcription	Spleen	Spleen
7	chr17:57167600-57183000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr17:57167800-57183000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr17:57168200-57183000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr17:57171200-57183400	Weak transcription	Small Intestine	intestine
11	chr17:57171400-57183000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr17:57171400-57183200	Weak transcription	Psoas Muscle	Psoas
13	chr17:57171600-57182800	Weak transcription	Adipose Nuclei	Adipose
14	chr17:57171600-57183200	Weak transcription	Colonic Mucosa	Colon
15	chr17:57171800-57183000	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr17:57172200-57182800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr17:57172400-57183200	Weak transcription	Ovary	ovary
18	chr17:57172600-57183400	Weak transcription	Left Ventricle	heart
19	chr17:57172600-57183400	Weak transcription	Lung	lung
20	chr17:57172800-57183200	Weak transcription	Placenta	Placenta
21	chr17:57173200-57183000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr17:57173200-57183000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr17:57175200-57183200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr17:57176000-57183000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr17:57176600-57183000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr17:57176600-57183400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr17:57177400-57183000	Weak transcription	Primary B cells from peripheral blood	blood
28	chr17:57177600-57183200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr17:57177800-57183000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr17:57177800-57183200	Weak transcription	Fetal Intestine Small	intestine
31	chr17:57178000-57183000	Weak transcription	Stomach Smooth Muscle	stomach
32	chr17:57178200-57182800	Weak transcription	Primary B cells from cord blood	blood
33	chr17:57178200-57183000	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr17:57178600-57183000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr17:57178600-57183000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr17:57178600-57183000	Weak transcription	Fetal Intestine Large	intestine
37	chr17:57178600-57183000	Weak transcription	Fetal Muscle Leg	muscle
38	chr17:57178600-57183000	Weak transcription	HSMMtube	muscle
39	chr17:57180600-57183000	Weak transcription	Liver	Liver
40	chr17:57181000-57183000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr17:57181200-57183000	Weak transcription	Fetal Stomach	stomach
42	chr17:57181400-57183000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr17:57181400-57183000	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr17:57181400-57183400	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr17:57181600-57182800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr17:57181600-57183000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr17:57181600-57183000	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr17:57181600-57183200	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr17:57181600-57183200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr17:57181600-57185200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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