Variant report

Variant	rs2870472
Chromosome Location	chr16:75278841-75278842
allele	C/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	NR2F2	chr16:75278814-75279639	MCF-7	breast:	n/a	n/a
8	SRF	chr16:75278838-75279420	HepG2	liver:	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
9	SPI1	chr16:75278736-75278887	GM12878	blood:	n/a	chr16:75278845-75278858
10	POLR2A	chr16:75277574-75279910	H1-hESC	embryonic stem cell:	n/a	n/a
11	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
12	JUND	chr16:75278200-75280079	SK-N-SH	brain:	n/a	chr16:75279432-75279446 chr16:75279214-75279225 chr16:75279216-75279227 chr16:75279218-75279227
13	NFIC	chr16:75278432-75279959	HepG2	liver:	n/a	n/a
14	GATA3	chr16:75278810-75279873	SK-N-SH	brain:	n/a	chr16:75279339-75279348 chr16:75279216-75279225 chr16:75278844-75278854
15	ARID3A	chr16:75278790-75279778	HepG2	liver:	n/a	n/a
16	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
17	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
18	MYBL2	chr16:75278285-75280014	HepG2	liver:	n/a	n/a
19	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
20	POLR2A	chr16:75277997-75279868	HepG2	liver:	n/a	n/a
21	CEBPD	chr16:75278828-75279745	HepG2	liver:	n/a	n/a
22	POLR2A	chr16:75278032-75286811	HepG2	liver:	n/a	n/a
23	POLR2A	chr16:75277156-75286603	IMR90	lung:	n/a	n/a
24	SMC3	chr16:75278240-75279853	Hela-S3	cervix:	n/a	chr16:75278618-75278628
25	RFX5	chr16:75278257-75279814	Hela-S3	cervix:	n/a	n/a
26	SPI1	chr16:75278711-75278938	K562	blood:	n/a	chr16:75278845-75278858
27	ZBTB7A	chr16:75278708-75279566	ECC-1	luminal epithelium:	n/a	chr16:75279037-75279045
28	POLR2A	chr16:75277186-75286167	HUVEC	blood vessel:	n/a	n/a
29	FOSL2	chr16:75278617-75279826	HepG2	liver:	n/a	chr16:75279432-75279446 chr16:75279215-75279226 chr16:75279214-75279225 chr16:75279218-75279227
30	MXI1	chr16:75278639-75279836	HepG2	liver:	n/a	chr16:75279561-75279570
31	HNF4A	chr16:75278710-75279427	HepG2	liver:	n/a	n/a
32	HDAC2	chr16:75278666-75279531	HepG2	liver:	n/a	chr16:75278904-75278918 chr16:75278899-75278913 chr16:75278903-75278917 chr16:75278905-75278919
33	POLR2A	chr16:75277560-75287530	HepG2	liver:	n/a	n/a
34	RCOR1	chr16:75278460-75279824	HepG2	liver:	n/a	n/a
35	HEY1	chr16:75278811-75279622	HepG2	liver:	n/a	chr16:75279562-75279571
36	RELA	chr16:75278681-75279546	GM12891	blood:	n/a	chr16:75279430-75279439 chr16:75279430-75279439
37	RCOR1	chr16:75278672-75282209	IMR90	lung:	n/a	n/a
38	NR2F2	chr16:75278839-75279556	MCF-7	breast:	n/a	n/a
39	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
40	RCOR1	chr16:75278627-75279313	GM12878	blood:	n/a	n/a
41	ZBTB7A	chr16:75278830-75279481	HepG2	liver:	n/a	chr16:75279037-75279045
42	TBP	chr16:75278603-75279804	HepG2	liver:	n/a	n/a
43	POLR2A	chr16:75277422-75283340	HUVEC	blood vessel:	n/a	n/a
44	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
45	TCF12	chr16:75278794-75279962	SK-N-SH	brain:	n/a	chr16:75279669-75279679 chr16:75279670-75279677
46	NFIC	chr16:75278789-75280007	SK-N-SH	brain:	n/a	n/a
47	YY1	chr16:75278835-75279060	GM12878	blood:	n/a	n/a
48	YY1	chr16:75278657-75278859	A549	lung:	n/a	n/a
49	RXRA	chr16:75278830-75279888	SK-N-SH	brain:	n/a	chr16:75278842-75278851
50	GATA3	chr16:75278823-75279842	MCF-7	breast:	n/a	chr16:75279339-75279348 chr16:75279216-75279225 chr16:75278844-75278854

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: 0)

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

rs_ID	r²[population]
rs1035540	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]
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	0.93[CEU][hapmap];1.00[MEX][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];0.92[TSI][hapmap];0.94[EUR][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[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][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	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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75269600-75280600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:75276600-75279200	Weak transcription	Fetal Brain Female	brain
3	chr16:75276600-75279400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr16:75276800-75283400	Enhancers	NHDF-Ad	bronchial
5	chr16:75276800-75283800	Enhancers	Left Ventricle	heart
6	chr16:75277000-75279000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr16:75277000-75279200	Enhancers	Aorta	Aorta
8	chr16:75277000-75280200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr16:75277000-75280200	Enhancers	Brain Substantia Nigra	brain
10	chr16:75277000-75281400	Enhancers	Brain Angular Gyrus	brain
11	chr16:75277000-75283400	Genic enhancers	Fetal Intestine Small	intestine
12	chr16:75277200-75279000	Enhancers	Right Ventricle	heart
13	chr16:75277200-75279200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr16:75277200-75279200	Enhancers	Brain Anterior Caudate	brain
15	chr16:75277200-75281600	Genic enhancers	Fetal Stomach	stomach
16	chr16:75277200-75284200	Enhancers	Spleen	Spleen
17	chr16:75277400-75281800	Enhancers	Adipose Nuclei	Adipose
18	chr16:75277400-75281800	Enhancers	Stomach Mucosa	stomach
19	chr16:75277400-75283400	Enhancers	Colon Smooth Muscle	Colon
20	chr16:75277600-75279000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr16:75277600-75279000	Enhancers	HMEC	breast
22	chr16:75277600-75279200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr16:75277600-75279200	Genic enhancers	Colonic Mucosa	Colon
24	chr16:75277600-75279600	Enhancers	Duodenum Mucosa	Duodenum
25	chr16:75277600-75280000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr16:75277600-75281200	Enhancers	Esophagus	oesophagus
27	chr16:75277600-75281400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr16:75277600-75281600	Flanking Active TSS	Stomach Smooth Muscle	stomach
29	chr16:75277600-75283200	Enhancers	Psoas Muscle	Psoas
30	chr16:75277600-75283600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr16:75277600-75283800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr16:75277600-75283800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr16:75277600-75283800	Enhancers	Ovary	ovary
34	chr16:75277600-75284000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr16:75277600-75284000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr16:75277600-75284000	Enhancers	Right Atrium	heart
37	chr16:75277600-75284400	Enhancers	Fetal Lung	lung
38	chr16:75277800-75279400	Flanking Active TSS	Brain Hippocampus Middle	brain
39	chr16:75277800-75279800	Enhancers	Brain Germinal Matrix	brain
40	chr16:75277800-75279800	Enhancers	Fetal Thymus	thymus
41	chr16:75277800-75280800	Enhancers	Lung	lung
42	chr16:75277800-75281800	Enhancers	HSMMtube	muscle
43	chr16:75277800-75282800	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr16:75277800-75284200	Enhancers	Liver	Liver
45	chr16:75278000-75279000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr16:75278000-75279000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr16:75278000-75279200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr16:75278000-75279200	Enhancers	Placenta	Placenta
49	chr16:75278000-75279200	Enhancers	Small Intestine	intestine
50	chr16:75278000-75279200	Genic enhancers	NHEK	skin

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