Variant report

Variant	rs7195583
Chromosome Location	chr16:30788182-30788183
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:109)
CpG islands
(count:0)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:109 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr16:30788040-30788190	GM12874	blood:	n/a	chr16:30788097-30788106
2	POLR2A	chr16:30788122-30788294	HepG2	liver:	n/a	n/a
3	CTCF	chr16:30788040-30788190	GM12873	blood:	n/a	chr16:30788097-30788106
4	KAP1	chr16:30788160-30788276	U2OS	brain:	n/a	n/a
5	KAP1	chr16:30788148-30788784	K562	blood:	n/a	n/a
6	CTCF	chr16:30788040-30788190	BJ	skin:	n/a	chr16:30788097-30788106
7	POLR2A	chr16:30788000-30788616	U87	brain:	n/a	n/a
8	CTCF	chr16:30788060-30788210	NB4	blood:	n/a	chr16:30788097-30788106
9	CTCF	chr16:30788060-30788210	HMEC	breast:	n/a	chr16:30788097-30788106
10	CTCF	chr16:30788060-30788210	GM12878	blood:	n/a	chr16:30788097-30788106
11	POLR2A	chr16:30788026-30788378	GM12878	blood:	n/a	n/a
12	CTCF	chr16:30787841-30788365	K562	blood:	n/a	chr16:30788097-30788106
13	POLR2A	chr16:30787767-30792226	K562	blood:	n/a	n/a
14	POLR2A	chr16:30785790-30788431	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr16:30788032-30789703	HepG2	liver:	n/a	n/a
16	CTCF	chr16:30788040-30788190	HRPEpiC	eye:	n/a	chr16:30788097-30788106
17	CTCF	chr16:30788040-30788190	WERI-Rb-1	eye:	n/a	chr16:30788097-30788106
18	POLR2A	chr16:30785774-30792079	PANC-1	pancreas:	n/a	n/a
19	CTCF	chr16:30788060-30788210	AG04449	skin:	n/a	chr16:30788097-30788106
20	CTCF	chr16:30788100-30788250	GM12869	blood:	n/a	n/a
21	POLR2A	chr16:30788132-30788347	MCF-7	breast:	n/a	n/a
22	NFYB	chr16:30788131-30788397	K562	blood:	n/a	chr16:30788259-30788274 chr16:30788263-30788275 chr16:30788259-30788274 chr16:30788262-30788272 chr16:30788261-30788274 chr16:30788260-30788274
23	POLR2A	chr16:30787921-30789650	ECC-1	luminal epithelium:	n/a	n/a
24	POLR2A	chr16:30785553-30792383	K562	blood:	n/a	n/a
25	POLR2A	chr16:30782383-30800309	HepG2	liver:	n/a	n/a
26	POLR2A	chr16:30787963-30789757	ECC-1	luminal epithelium:	n/a	n/a
27	POLR2A	chr16:30787944-30788454	GM12891	blood:	n/a	n/a
28	POLR2A	chr16:30788158-30790879	HepG2	liver:	n/a	n/a
29	POLR2A	chr16:30788105-30788353	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr16:30788013-30790558	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr16:30787773-30789652	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr16:30788001-30792932	HepG2	liver:	n/a	n/a
33	POLR2A	chr16:30787899-30788419	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr16:30786429-30791257	MCF10A-Er-Src	breast:	n/a	n/a
35	CTCF	chr16:30788040-30788190	HFF-Myc	foreskin:	n/a	chr16:30788097-30788106
36	HEY1	chr16:30787911-30788954	K562	blood:	n/a	n/a
37	POLR2A	chr16:30788082-30789521	HepG2	liver:	n/a	n/a
38	MTA3	chr16:30787925-30788861	GM12878	blood:	n/a	n/a
39	POLR2A	chr16:30785480-30792632	SK-N-MC	brain:	n/a	n/a
40	MBD4	chr16:30787976-30790178	HepG2	liver:	n/a	n/a
41	CTCF	chr16:30788060-30788210	NHDF-neo	bronchial:	n/a	chr16:30788097-30788106
42	POLR2A	chr16:30782939-30789605	GM12878	blood:	n/a	n/a
43	TEAD4	chr16:30788012-30788752	K562	blood:	n/a	n/a
44	POLR2A	chr16:30788068-30790778	HepG2	liver:	n/a	n/a
45	CTCF	chr16:30788080-30788230	NHDF-neo	bronchial:	n/a	chr16:30788097-30788106
46	NFATC1	chr16:30787945-30788317	GM12878	blood:	n/a	n/a
47	POLR2A	chr16:30788124-30788355	A549	lung:	n/a	n/a
48	POLR2A	chr16:30788085-30791665	MCF-7	breast:	n/a	n/a
49	POLR2A	chr16:30788067-30788409	GM12891	blood:	n/a	n/a
50	EBF1	chr16:30787978-30788319	GM12878	blood:	n/a	n/a

No data

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30785578..30788254-chr16:30911758..30913330,2	K562	blood:
2	chr16:30750130..30751710-chr16:30786597..30789576,2	K562	blood:
3	chr16:30786955..30788524-chr16:30856024..30857941,2	MCF-7	breast:
4	chr16:30787031..30789768-chr16:30814722..30816994,3	K562	blood:
5	chr16:30672949..30675838-chr16:30787007..30788848,2	K562	blood:
6	chr16:30786166..30788265-chr16:30885504..30887644,2	K562	blood:
7	chr16:30785888..30788554-chr16:30910264..30913516,3	MCF-7	breast:
8	chr16:30787386..30789402-chr16:30849116..30851160,2	MCF-7	breast:
9	chr16:30709167..30713119-chr16:30785919..30788328,5	MCF-7	breast:
10	chr16:30785755..30789519-chr16:30993933..30997614,3	K562	blood:
11	chr16:30786009..30790115-chr16:30903648..30907620,6	MCF-7	breast:
12	chr16:30786609..30788536-chr16:30898139..30900577,3	K562	blood:
13	chr16:30786539..30788362-chr16:30912397..30914533,2	MCF-7	breast:
14	chr16:30787481..30790193-chr16:30968511..30970450,2	K562	blood:
15	chr16:30785759..30789223-chr16:30822658..30825886,4	K562	blood:
16	chr16:30787481..30790093-chr16:30968266..30970450,2	K562	blood:
17	chr16:30369515..30371729-chr16:30786723..30788933,2	MCF-7	breast:
18	chr16:30786896..30788399-chr16:30817095..30819467,2	K562	blood:
19	chr16:30785822..30789729-chr16:30809078..30811832,3	K562	blood:
20	chr16:30786121..30788746-chr16:30845072..30846818,3	K562	blood:
21	chr16:30786387..30788885-chr16:30817095..30819249,4	K562	blood:
22	chr16:30783772..30791593-chr16:30931071..30936822,9	MCF-7	breast:
23	chr16:30786822..30789085-chr16:30886328..30888758,2	MCF-7	breast:
24	chr16:30785189..30790485-chr16:30931540..30936077,12	K562	blood:
25	chr16:30726174..30728075-chr16:30787184..30789746,3	K562	blood:
26	chr16:30756700..30760166-chr16:30785453..30788232,3	MCF-7	breast:
27	chr16:30405512..30407718-chr16:30786792..30789552,2	MCF-7	breast:
28	chr16:30784974..30791554-chr16:30930641..30936449,8	MCF-7	breast:
29	chr16:30749452..30756542-chr16:30785692..30792123,12	MCF-7	breast:
30	chr16:30707557..30712450-chr16:30785751..30791890,10	K562	blood:
31	chr16:30707849..30711301-chr16:30785397..30790684,8	K562	blood:
32	chr1:200723441..200726355-chr16:30786271..30788267,2	MCF-7	breast:
33	chr16:30785870..30788311-chr16:31468654..31470715,2	K562	blood:
34	chr16:30671278..30673717-chr16:30785023..30788710,4	MCF-7	breast:
35	chr16:30785189..30790485-chr16:30931540..30935208,7	K562	blood:
36	chr16:30787489..30791955-chr16:30902887..30909666,10	K562	blood:

No data

Variant related genes	Relation type
ENSG00000262026	TF binding region
ENSG00000099385	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000260852	Chromatin interaction
ENSG00000169221	Chromatin interaction
ENSG00000268863	Chromatin interaction
ENSG00000222287	Chromatin interaction
ENSG00000099364	Chromatin interaction
ENSG00000156860	Chromatin interaction
ENSG00000156873	Chromatin interaction
ENSG00000211591	Chromatin interaction
ENSG00000180096	Chromatin interaction
ENSG00000099377	Chromatin interaction
ENSG00000150281	Chromatin interaction
ENSG00000099381	Chromatin interaction
ENSG00000260083	Chromatin interaction
ENSG00000265991	Chromatin interaction
ENSG00000262721	Chromatin interaction
ENSG00000260899	Chromatin interaction
ENSG00000180035	Chromatin interaction
ENSG00000080603	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10782000	0.94[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11150594	1.00[AMR][1000 genomes]
rs11150595	0.87[ASW][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap]
rs11640414	0.82[AFR][1000 genomes]
rs11648654	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12447824	0.85[AFR][1000 genomes]
rs12596375	0.87[ASW][hapmap];1.00[AMR][1000 genomes]
rs12596394	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12598056	1.00[AMR][1000 genomes]
rs12931844	1.00[AMR][1000 genomes]
rs12933849	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1530203	0.87[ASW][hapmap];0.83[YRI][hapmap]
rs1550477	0.87[ASW][hapmap];0.92[MKK][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2053426	1.00[AMR][1000 genomes]
rs2099754	0.87[ASW][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2099755	0.87[ASW][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2919430	1.00[AMR][1000 genomes]
rs2919431	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2919432	1.00[LWK][hapmap];0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs2919433	1.00[AMR][1000 genomes]
rs2972804	1.00[AMR][1000 genomes]
rs2972808	0.81[LWK][hapmap];0.82[YRI][hapmap]
rs2972809	0.81[LWK][hapmap];0.81[YRI][hapmap]
rs2972815	1.00[AMR][1000 genomes]
rs4617878	0.87[ASW][hapmap];0.92[MKK][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4889488	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4889494	1.00[AMR][1000 genomes]
rs4889500	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs4889501	1.00[AMR][1000 genomes]
rs4889503	1.00[LWK][hapmap];0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs4889504	0.87[ASW][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4889505	1.00[LWK][hapmap];0.94[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4889508	0.88[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4889509	0.87[ASW][hapmap];1.00[YRI][hapmap]
rs4889510	1.00[AMR][1000 genomes]
rs4889528	1.00[AMR][1000 genomes]
rs55635617	1.00[AMR][1000 genomes]
rs56038936	1.00[AMR][1000 genomes]
rs56209507	1.00[AMR][1000 genomes]
rs57225118	1.00[AMR][1000 genomes]
rs57643871	1.00[AMR][1000 genomes]
rs57877247	1.00[AMR][1000 genomes]
rs6565198	0.83[YRI][hapmap]
rs6565203	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6565204	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6565205	1.00[AMR][1000 genomes]
rs6565208	1.00[ASW][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs6565209	1.00[AMR][1000 genomes]
rs6565210	1.00[AMR][1000 genomes]
rs7185136	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7188077	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7193412	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7194763	1.00[AMR][1000 genomes]
rs7195612	0.86[ASW][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs73524581	1.00[AMR][1000 genomes]
rs73524584	1.00[AMR][1000 genomes]
rs73536457	1.00[AMR][1000 genomes]
rs73536466	1.00[AMR][1000 genomes]
rs73536474	1.00[AMR][1000 genomes]
rs73536488	1.00[AMR][1000 genomes]
rs73536498	1.00[AMR][1000 genomes]
rs73536499	1.00[AMR][1000 genomes]
rs8045484	0.87[ASW][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap]
rs8045550	1.00[AMR][1000 genomes]
rs8045624	0.87[ASW][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs8046609	1.00[AMR][1000 genomes]
rs8047743	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8048656	1.00[LWK][hapmap];0.94[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8049589	1.00[AMR][1000 genomes]
rs8050578	0.93[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8056105	0.85[AFR][1000 genomes]
rs8058475	1.00[AMR][1000 genomes]
rs893926	0.94[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs893927	0.87[ASW][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9921630	0.87[ASW][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9934046	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9941201	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9941300	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][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	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv469724	chr16:30632445-30840263	Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
4	nsv482704	chr16:30632445-30840263	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS 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	143 gene(s)	inside rSNPs	diseases
5	nsv833188	chr16:30632446-30840263	Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
6	nsv1064134	chr16:30640293-31087327	Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
7	nsv905728	chr16:30642867-30928970	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	171 gene(s)	inside rSNPs	diseases
8	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
9	esv1825223	chr16:30669091-30971810	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
10	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
11	nsv9438	chr16:30770203-30799442	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
12	nsv905732	chr16:30788182-30837210	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30786200-30788200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr16:30786200-30788200	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr16:30786200-30788400	Active TSS	H9 Cell Line	embryonic stem cell
4	chr16:30786200-30788400	Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr16:30786400-30788200	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr16:30786400-30788200	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr16:30786400-30788200	Active TSS	Fetal Kidney	kidney
8	chr16:30786600-30788200	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr16:30786600-30788200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr16:30786600-30788800	Active TSS	Rectal Smooth Muscle	rectum
11	chr16:30786800-30788400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
12	chr16:30787000-30788200	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr16:30787000-30788800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr16:30787400-30788200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
15	chr16:30787400-30788200	Flanking Active TSS	Fetal Muscle Leg	muscle
16	chr16:30787400-30788600	Flanking Active TSS	Duodenum Mucosa	Duodenum
17	chr16:30787400-30788800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr16:30787400-30790400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr16:30787600-30788200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr16:30787600-30788200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
21	chr16:30787600-30788200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr16:30787600-30788200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr16:30787600-30788200	Enhancers	Aorta	Aorta
24	chr16:30787600-30788200	Flanking Active TSS	Fetal Intestine Small	intestine
25	chr16:30787600-30788200	Weak transcription	Small Intestine	intestine
26	chr16:30787600-30788200	Enhancers	Spleen	Spleen
27	chr16:30787600-30788400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr16:30787600-30788400	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr16:30787600-30788400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr16:30787600-30788400	Enhancers	Brain Germinal Matrix	brain
31	chr16:30787600-30788400	Enhancers	Placenta Amnion	Placenta Amnion
32	chr16:30787600-30788600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr16:30787600-30789000	Enhancers	Gastric	stomach
34	chr16:30787600-30789200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr16:30787600-30789400	Enhancers	Stomach Mucosa	stomach
36	chr16:30787600-30793000	Weak transcription	Esophagus	oesophagus
37	chr16:30787600-30793400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr16:30787600-30797600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr16:30787800-30788200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr16:30787800-30788200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr16:30787800-30788200	Enhancers	Primary B cells from cord blood	blood
42	chr16:30787800-30788200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr16:30787800-30788200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr16:30787800-30788200	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr16:30787800-30788200	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr16:30787800-30788200	Enhancers	Fetal Brain Male	brain
47	chr16:30787800-30788200	Flanking Active TSS	Fetal Intestine Large	intestine
48	chr16:30787800-30788200	Enhancers	Fetal Lung	lung
49	chr16:30787800-30788200	Weak transcription	Right Atrium	heart
50	chr16:30787800-30788200	Enhancers	NHEK	skin

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