Variant report

Variant	rs1035540
Chromosome Location	chr16:75278795-75278796
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	TCF12	chr16:75278578-75279901	A549	lung:	n/a	chr16:75279669-75279679 chr16:75279670-75279677
2	NFIC	chr16:75278726-75279614	HepG2	liver:	n/a	n/a
3	SPI1	chr16:75278609-75279034	GM12891	blood:	n/a	chr16:75278845-75278858
4	POLR2A	chr16:75276865-75287749	HepG2	liver:	n/a	n/a
5	POLR2A	chr16:75278284-75280237	U87	brain:	n/a	n/a
6	POLR2A	chr16:75278570-75279700	HepG2	liver:	n/a	n/a
7	SPI1	chr16:75278736-75278887	GM12878	blood:	n/a	chr16:75278845-75278858
8	POLR2A	chr16:75277574-75279910	H1-hESC	embryonic stem cell:	n/a	n/a
9	SRF	chr16:75278467-75279938	HCT-116	colon:	n/a	chr16:75279074-75279087 chr16:75279076-75279087 chr16:75279072-75279086 chr16:75279075-75279086 chr16:75279072-75279089 chr16:75279073-75279088 chr16:75279074-75279087 chr16:75279076-75279085 chr16:75279003-75279013 chr16:75279071-75279089 chr16:75279074-75279085
10	JUND	chr16:75278200-75280079	SK-N-SH	brain:	n/a	chr16:75279432-75279446 chr16:75279214-75279225 chr16:75279216-75279227 chr16:75279218-75279227
11	NFIC	chr16:75278432-75279959	HepG2	liver:	n/a	n/a
12	ARID3A	chr16:75278790-75279778	HepG2	liver:	n/a	n/a
13	MAZ	chr16:75277507-75280033	IMR90	lung:	n/a	chr16:75279563-75279570 chr16:75279562-75279571 chr16:75279003-75279013 chr16:75279620-75279630 chr16:75279561-75279571 chr16:75279553-75279569 chr16:75279390-75279400 chr16:75279562-75279571 chr16:75279682-75279692 chr16:75279561-75279572 chr16:75279561-75279572
14	MAX	chr16:75278757-75279995	HCT-116	colon:	n/a	chr16:75279563-75279570 chr16:75279562-75279571 chr16:75279003-75279013 chr16:75279620-75279630 chr16:75279561-75279571 chr16:75279553-75279569 chr16:75279390-75279400 chr16:75279562-75279571 chr16:75279682-75279692 chr16:75279561-75279572 chr16:75279561-75279572
15	MYBL2	chr16:75278285-75280014	HepG2	liver:	n/a	n/a
16	MYC	chr16:75278503-75279999	A549	lung:	n/a	chr16:75279563-75279570 chr16:75279562-75279571 chr16:75279003-75279013 chr16:75279620-75279630 chr16:75279561-75279571 chr16:75279553-75279569 chr16:75279390-75279400 chr16:75279562-75279571 chr16:75279682-75279692 chr16:75279561-75279572 chr16:75279561-75279572
17	POLR2A	chr16:75277997-75279868	HepG2	liver:	n/a	n/a
18	POLR2A	chr16:75278032-75286811	HepG2	liver:	n/a	n/a
19	POLR2A	chr16:75277156-75286603	IMR90	lung:	n/a	n/a
20	SMC3	chr16:75278240-75279853	Hela-S3	cervix:	n/a	chr16:75278618-75278628
21	RFX5	chr16:75278257-75279814	Hela-S3	cervix:	n/a	n/a
22	SPI1	chr16:75278711-75278938	K562	blood:	n/a	chr16:75278845-75278858
23	ZBTB7A	chr16:75278708-75279566	ECC-1	luminal epithelium:	n/a	chr16:75279037-75279045
24	POLR2A	chr16:75277186-75286167	HUVEC	blood vessel:	n/a	n/a
25	FOSL2	chr16:75278617-75279826	HepG2	liver:	n/a	chr16:75279432-75279446 chr16:75279215-75279226 chr16:75279214-75279225 chr16:75279218-75279227
26	MXI1	chr16:75278639-75279836	HepG2	liver:	n/a	chr16:75279561-75279570
27	HNF4A	chr16:75278710-75279427	HepG2	liver:	n/a	n/a
28	HDAC2	chr16:75278666-75279531	HepG2	liver:	n/a	chr16:75278904-75278918 chr16:75278899-75278913 chr16:75278903-75278917 chr16:75278905-75278919
29	POLR2A	chr16:75277560-75287530	HepG2	liver:	n/a	n/a
30	RCOR1	chr16:75278460-75279824	HepG2	liver:	n/a	n/a
31	RELA	chr16:75278681-75279546	GM12891	blood:	n/a	chr16:75279430-75279439 chr16:75279430-75279439
32	RCOR1	chr16:75278672-75282209	IMR90	lung:	n/a	n/a
33	SP1	chr16:75278695-75279618	HepG2	liver:	n/a	chr16:75279002-75279014 chr16:75279119-75279128 chr16:75278999-75279013 chr16:75279120-75279129 chr16:75279003-75279012 chr16:75279002-75279014
34	RCOR1	chr16:75278627-75279313	GM12878	blood:	n/a	n/a
35	TBP	chr16:75278603-75279804	HepG2	liver:	n/a	n/a
36	POLR2A	chr16:75277422-75283340	HUVEC	blood vessel:	n/a	n/a
37	MAX	chr16:75278147-75280130	HepG2	liver:	n/a	chr16:75279563-75279570 chr16:75279562-75279571 chr16:75279003-75279013 chr16:75279620-75279630 chr16:75279561-75279571 chr16:75279553-75279569 chr16:75279390-75279400 chr16:75279562-75279571 chr16:75279682-75279692 chr16:75279561-75279572 chr16:75279561-75279572
38	TCF12	chr16:75278794-75279962	SK-N-SH	brain:	n/a	chr16:75279669-75279679 chr16:75279670-75279677
39	NFIC	chr16:75278789-75280007	SK-N-SH	brain:	n/a	n/a
40	YY1	chr16:75278657-75278859	A549	lung:	n/a	n/a
41	SIN3AK20	chr16:75278777-75279981	MCF-7	breast:	n/a	n/a
42	TCF12	chr16:75278663-75280055	SK-N-SH	brain:	n/a	chr16:75279669-75279679 chr16:75279670-75279677
43	TEAD4	chr16:75278632-75279921	HepG2	liver:	n/a	n/a
44	GATA3	chr16:75278779-75279904	A549	lung:	n/a	chr16:75279339-75279348 chr16:75279216-75279225 chr16:75278844-75278854
45	EBF1	chr16:75278590-75279611	GM12878	blood:	n/a	chr16:75279133-75279144
46	EP300	chr16:75278744-75279756	HepG2	liver:	n/a	chr16:75278842-75278856 chr16:75278902-75278916 chr16:75278900-75278914 chr16:75278904-75278918
47	SPI1	chr16:75278444-75279234	GM12878	blood:	n/a	chr16:75278845-75278858
48	MBD4	chr16:75278518-75279831	HepG2	liver:	n/a	n/a
49	EP300	chr16:75278704-75279718	HepG2	liver:	n/a	chr16:75278842-75278856 chr16:75278902-75278916 chr16:75278722-75278730 chr16:75278900-75278914 chr16:75278904-75278918
50	SPI1	chr16:75278606-75279040	GM12891	blood:	n/a	chr16:75278845-75278858

No.	Distal block	Cell Line	Cell type
1	chr16:75277872..75280775-chr16:75339667..75341248,2	MCF-7	breast:
2	chr16:75270029..75275734-chr16:75275780..75279452,5	K562	blood:
3	chr16:75278019..75280837-chr16:75435564..75439238,4	MCF-7	breast:
4	chr16:75278100..75280781-chr16:75467014..75469094,2	MCF-7	breast:

Variant related genes	Relation type
BCAR1	TF binding region
ENSG00000050820	Chromatin interaction
ENSG00000153774	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1107593	0.84[CEU][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11149811	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11641896	0.97[EUR][1000 genomes]
rs12918452	0.81[EUR][1000 genomes]
rs12924999	1.00[ASW][hapmap];0.93[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1808427	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1862738	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2870471	0.87[CEU][hapmap];1.00[GIH][hapmap];0.92[TSI][hapmap];0.94[EUR][1000 genomes]
rs2870472	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3169330	0.86[CEU][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes]
rs4737	0.93[CEU][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes]
rs4888361	0.96[EUR][1000 genomes]
rs4888362	1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs4888363	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4888364	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4888365	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6564239	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs6564241	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6564243	0.97[EUR][1000 genomes]
rs7195938	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7202566	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8048371	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8048956	0.93[CEU][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8057145	1.00[ASW][hapmap];0.93[CEU][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8059190	0.91[EUR][1000 genomes]
rs8061356	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs889514	0.93[EUR][1000 genomes]
rs889515	1.00[ASW][hapmap];0.93[CEU][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9319481	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9927264	0.93[CEU][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9928842	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061095	chr16:74519718-75407020	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv532560	chr16:74692406-75411912	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
3	nsv916502	chr16:74845880-75732365	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	131 gene(s)	inside rSNPs	diseases
4	nsv1056082	chr16:75004990-75295847	Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer Genic enhancers 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	47 gene(s)	inside rSNPs	diseases
5	nsv833282	chr16:75154171-75330634	Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
6	nsv516504	chr16:75223491-75306402	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	nsv523405	chr16:75227969-75342846	Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
8	esv1806781	chr16:75235390-75307470	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Active 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	24 gene(s)	inside rSNPs	diseases
9	nsv906909	chr16:75236154-75316074	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
10	esv1792587	chr16:75237936-75305783	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
11	nsv906910	chr16:75251299-75316074	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
12	nsv906911	chr16:75252526-75296247	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv906912	chr16:75252526-75320827	Flanking Active TSS Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
14	esv1813349	chr16:75257361-75302684	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
15	nsv931939	chr16:75261354-75765025	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
16	nsv906913	chr16:75267743-75306402	Genic enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
17	nsv471095	chr16:75269533-75320827	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
18	esv1843498	chr16:75271642-75296844	Genic enhancers Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
19	nsv978002	chr16:75274402-75288324	Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1035540	EXOSC6	cis	parietal	SCAN
rs1035540	CNTNAP4	cis	parietal	SCAN

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75266600-75278800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr16:75269600-75280600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:75270400-75278800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr16:75272800-75278800	Genic enhancers	Gastric	stomach
5	chr16:75276600-75279200	Weak transcription	Fetal Brain Female	brain
6	chr16:75276600-75279400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr16:75276800-75283400	Enhancers	NHDF-Ad	bronchial
8	chr16:75276800-75283800	Enhancers	Left Ventricle	heart
9	chr16:75277000-75279000	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr16:75277000-75279200	Enhancers	Aorta	Aorta
11	chr16:75277000-75280200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr16:75277000-75280200	Enhancers	Brain Substantia Nigra	brain
13	chr16:75277000-75281400	Enhancers	Brain Angular Gyrus	brain
14	chr16:75277000-75283400	Genic enhancers	Fetal Intestine Small	intestine
15	chr16:75277200-75279000	Enhancers	Right Ventricle	heart
16	chr16:75277200-75279200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr16:75277200-75279200	Enhancers	Brain Anterior Caudate	brain
18	chr16:75277200-75281600	Genic enhancers	Fetal Stomach	stomach
19	chr16:75277200-75284200	Enhancers	Spleen	Spleen
20	chr16:75277400-75281800	Enhancers	Adipose Nuclei	Adipose
21	chr16:75277400-75281800	Enhancers	Stomach Mucosa	stomach
22	chr16:75277400-75283400	Enhancers	Colon Smooth Muscle	Colon
23	chr16:75277600-75278800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr16:75277600-75278800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr16:75277600-75278800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr16:75277600-75279000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr16:75277600-75279000	Enhancers	HMEC	breast
28	chr16:75277600-75279200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr16:75277600-75279200	Genic enhancers	Colonic Mucosa	Colon
30	chr16:75277600-75279600	Enhancers	Duodenum Mucosa	Duodenum
31	chr16:75277600-75280000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr16:75277600-75281200	Enhancers	Esophagus	oesophagus
33	chr16:75277600-75281400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr16:75277600-75281600	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr16:75277600-75283200	Enhancers	Psoas Muscle	Psoas
36	chr16:75277600-75283600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr16:75277600-75283800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr16:75277600-75283800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr16:75277600-75283800	Enhancers	Ovary	ovary
40	chr16:75277600-75284000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr16:75277600-75284000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr16:75277600-75284000	Enhancers	Right Atrium	heart
43	chr16:75277600-75284400	Enhancers	Fetal Lung	lung
44	chr16:75277800-75278800	Genic enhancers	Rectal Mucosa Donor 29	rectum
45	chr16:75277800-75279400	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr16:75277800-75279800	Enhancers	Brain Germinal Matrix	brain
47	chr16:75277800-75279800	Enhancers	Fetal Thymus	thymus
48	chr16:75277800-75280800	Enhancers	Lung	lung
49	chr16:75277800-75281800	Enhancers	HSMMtube	muscle
50	chr16:75277800-75282800	Enhancers	Rectal Mucosa Donor 31	rectum

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