Variant report

Variant	nsv9459
Chromosome Location	chr16:75274167-75277500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:120)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:120 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr16:75274919-75275235	GM12878	blood:	n/a	n/a
2	CTCF	chr16:75276413-75276434	MCF-7	breast:	n/a	n/a
3	CTCF	chr16:75274640-75274790	HBMEC	blood vessel:	n/a	n/a
4	CTCF	chr16:75276397-75276532	GM20000	blood:	n/a	n/a
5	CTCF	chr16:75275580-75275730	HEEpiC	esophagus:	n/a	n/a
6	CTCF	chr16:75274640-75274790	HPAF	blood vessel:	n/a	n/a
7	CTCF	chr16:75274700-75274850	HAc	cerebellar:	n/a	n/a
8	CTCF	chr16:75274720-75274870	BE2_C	brain:	n/a	n/a
9	CTCF	chr16:75275580-75275730	SAEC	small airway:	n/a	n/a
10	CTCF	chr16:75274680-75274830	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr16:75274680-75274830	HPF	lung:	n/a	n/a
12	CTCF	chr16:75274581-75274655	Spleen_OC	spleen:	n/a	n/a
13	CTCF	chr16:75275420-75275570	HMEC	breast:	n/a	chr16:75275500-75275509 chr16:75275494-75275512
14	CTCF	chr16:75274660-75274810	HA-sp	spinal cord:	n/a	n/a
15	CTCF	chr16:75274740-75274890	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr16:75275340-75275490	HEK293	kidney:	n/a	n/a
17	CTCF	chr16:75275480-75275630	HepG2	liver:	n/a	chr16:75275500-75275509 chr16:75275494-75275512
18	CTCF	chr16:75274680-75274830	AG04449	skin:	n/a	n/a
19	CTCF	chr16:75274695-75274829	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr16:75275340-75275490	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr16:75275320-75275470	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr16:75275152-75275243	GM19239	blood:	n/a	n/a
23	CTCF	chr16:75275320-75275570	GM12872	blood:	n/a	chr16:75275500-75275509 chr16:75275494-75275512
24	CTCF	chr16:75274780-75274930	HAc	cerebellar:	n/a	n/a
25	CTCF	chr16:75274620-75274770	BJ	skin:	n/a	n/a
26	CTCF	chr16:75274660-75274810	AG04450	lung:	n/a	n/a
27	CTCF	chr16:75274680-75274830	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr16:75274882-75274897	LNCaP	prostate:	n/a	n/a
29	CTCF	chr16:75274660-75274810	GM06990	blood:	n/a	n/a
30	CTCF	chr16:75275620-75275770	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr16:75275460-75275610	GM12864	blood:	n/a	chr16:75275500-75275509 chr16:75275494-75275512
32	MAZ	chr16:75271480-75274285	IMR90	lung:	n/a	chr16:75273779-75273788 chr16:75272890-75272897 chr16:75273779-75273789 chr16:75271860-75271870 chr16:75273778-75273791 chr16:75273779-75273790 chr16:75273780-75273789 chr16:75273781-75273788 chr16:75274103-75274112 chr16:75273061-75273070 chr16:75273780-75273790 chr16:75273435-75273445
33	NFATC1	chr16:75274895-75275281	GM12878	blood:	n/a	n/a
34	PBX3	chr16:75275117-75275280	GM12878	blood:	n/a	n/a
35	POLR2A	chr16:75274775-75275549	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr16:75276052-75276414	A549	lung:	n/a	n/a
37	POLR2A	chr16:75276014-75276617	U87	brain:	n/a	n/a
38	POLR2A	chr16:75275726-75275943	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr16:75275792-75275950	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr16:75275816-75276324	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr16:75276050-75276242	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr16:75276083-75276210	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr16:75274943-75275314	HepG2	liver:	n/a	n/a
44	POLR2A	chr16:75275734-75276444	A549	lung:	n/a	n/a
45	POLR2A	chr16:75274783-75275356	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr16:75275241-75276732	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr16:75274949-75275244	MCF-7	breast:	n/a	n/a
48	POLR2A	chr16:75277156-75286603	IMR90	lung:	n/a	n/a
49	POLR2A	chr16:75274873-75275197	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr16:75276857-75277388	HUVEC	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75275068-75275118	AG10803	skin:	n/a
2	chr16:75275068-75275118	LNCaP	prostate:	n/a
3	chr16:75276399-75276449	ovcar-3	ovarian:	n/a
4	chr16:75276399-75276449	HEEpiC	esophagus:	n/a
5	chr16:75275068-75275118	K562	blood:	n/a
6	chr16:75275068-75275118	GM19239	blood:	n/a
7	chr16:75275068-75275118	HepG2	liver:	n/a
8	chr16:75275068-75275118	SK-N-SH	brain:	n/a
9	chr16:75276399-75276449	AG09319	gingival:	n/a
10	chr16:75276399-75276449	HAEpiC	amniotic membrane:	n/a
11	chr16:75276399-75276449	GM12878	blood:	n/a
12	chr16:75275068-75275118	HIPEpiC	eye:	n/a
13	chr16:75276399-75276449	Hepatocyte	liver:	n/a
14	chr16:75276399-75276449	Caco-2	colon:	n/a
15	chr16:75275068-75275118	NT2-D1	testis:	n/a
16	chr16:75276399-75276449	SAEC	small airway:	n/a
17	chr16:75276399-75276449	HIPEpiC	eye:	n/a
18	chr16:75275068-75275118	NHDF-neo	bronchial:	n/a
19	chr16:75275068-75275118	AoSMC	blood vessel:	n/a
20	chr16:75276399-75276449	MCF10A-Er-Src	breast:	n/a
21	chr16:75276399-75276449	LNCaP	prostate:	n/a
22	chr16:75275068-75275118	AG09319	gingival:	n/a
23	chr16:75275068-75275118	SAEC	small airway:	n/a
24	chr16:75275068-75275118	HAEpiC	amniotic membrane:	n/a
25	chr16:75276399-75276449	HepG2	liver:	n/a
26	chr16:75276399-75276449	MCF-7	breast:	n/a
27	chr16:75276399-75276449	HRPEpiC	eye:	n/a
28	chr16:75275068-75275118	GM06990	blood:	n/a
29	chr16:75275068-75275118	H1-hESC	embryonic stem cell:	embryo
30	chr16:75275068-75275118	HEEpiC	esophagus:	n/a
31	chr16:75275068-75275118	NHBE	bronchial:	n/a
32	chr16:75276399-75276449	PANC-1	pancreas:	n/a
33	chr16:75275068-75275118	GM12878	blood:	n/a
34	chr16:75275068-75275118	GM12891	blood:	n/a
35	chr16:75275068-75275118	A549	lung:	n/a
36	chr16:75275068-75275118	IMR90	lung:	fetal
37	chr16:75275068-75275118	HL-60	blood:	n/a
38	chr16:75275068-75275118	HCF	heart:	n/a
39	chr16:75275068-75275118	HRPEpiC	eye:	n/a
40	chr16:75276399-75276449	GM12892	blood:	n/a
41	chr16:75275068-75275118	Hela-S3	cervix:	n/a
42	chr16:75275068-75275118	Hepatocyte	liver:	n/a
43	chr16:75275068-75275118	NH-A	brain:	n/a
44	chr16:75276399-75276449	BE2_C	brain:	n/a
45	chr16:75276399-75276449	ProgFib	skin:	n/a
46	chr16:75275068-75275118	Jurkat	blood:	n/a
47	chr16:75276399-75276449	AoSMC	blood vessel:	n/a
48	chr16:75276399-75276449	AG04449	skin:	fetal
49	chr16:75275068-75275118	HPAEpiC	pulmonary alveolar:	n/a
50	chr16:75275068-75275118	AG09309	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:75260096..75262598-chr16:75274071..75277051,2	K562	blood:
2	chr16:75270029..75275734-chr16:75275780..75279452,5	K562	blood:
3	chr16:75270029..75275734-chr16:75275780..75279452,5	K562	blood:
4	chr16:75258215..75260449-chr16:75277050..75278735,2	K562	blood:
5	chr16:75271441..75274374-chr6:74228830..74231678,2	MCF-7	breast:
6	chr16:75271644..75278130-chr16:75410170..75415316,7	MCF-7	breast:
7	chr16:75268472..75270421-chr16:75272805..75274376,2	MCF-7	breast:
8	chr16:75266165..75267997-chr16:75273456..75276001,2	K562	blood:
9	chr16:75271315..75273372-chr16:75275391..75277280,2	K562	blood:

No data

Variant related genes	Relation type
BCAR1	TF binding region
BCAR1	CpG island
ENSG00000050820	chromatin interactions
ENSG00000261783	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000240338	chromatin interactions

Extended variants
information (count: 219 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:219 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533842647	chr16:75274220-75274221	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs560544851	chr16:75274232-75274233	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs3784938	chr16:75274235-75274236	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs188316770	chr16:75274261-75274262	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs2870471	chr16:75274282-75274283	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs181085922	chr16:75274293-75274294	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs576584119	chr16:75274299-75274300	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs184255528	chr16:75274311-75274312	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs576575772	chr16:75274317-75274318	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs527647134	chr16:75274326-75274327	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs545484293	chr16:75274347-75274348	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs564621323	chr16:75274433-75274434	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs533615820	chr16:75274448-75274449	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs550094068	chr16:75274452-75274453	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs189856107	chr16:75274462-75274463	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs9921054	chr16:75274498-75274499	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs547848690	chr16:75274519-75274520	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs567719323	chr16:75274539-75274540	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs531281852	chr16:75274548-75274549	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs547707933	chr16:75274562-75274563	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs570638177	chr16:75274583-75274584	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs369827883	chr16:75274619-75274620	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs140180674	chr16:75274625-75274626	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs113975127	chr16:75274660-75274661	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs527889859	chr16:75274704-75274705	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs150334983	chr16:75274715-75274716	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs535962145	chr16:75274736-75274737	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs144892750	chr16:75274744-75274745	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs572520550	chr16:75274746-75274747	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs541058414	chr16:75274760-75274761	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs564837300	chr16:75274765-75274766	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs578173993	chr16:75274776-75274777	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs544068133	chr16:75274780-75274781	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs563558264	chr16:75274817-75274818	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs181775956	chr16:75274818-75274819	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs539070786	chr16:75274841-75274842	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs547926521	chr16:75274848-75274849	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs575508875	chr16:75274853-75274854	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs561436040	chr16:75274868-75274869	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs527313714	chr16:75274872-75274873	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs547055573	chr16:75274897-75274898	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs570399545	chr16:75274912-75274913	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs372633042	chr16:75274931-75274932	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs539366043	chr16:75274947-75274948	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs550007288	chr16:75274958-75274959	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs186892983	chr16:75274959-75274960	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs535643799	chr16:75274963-75274964	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs190630665	chr16:75274965-75274966	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs370469365	chr16:75274966-75274967	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs572556503	chr16:75274969-75274970	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75260800-75278000	Weak transcription	Small Intestine	intestine
2	chr16:75262000-75277400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
3	chr16:75263200-75274800	Weak transcription	Fetal Kidney	kidney
4	chr16:75264200-75274800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr16:75266600-75278800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr16:75268000-75277200	Genic enhancers	Spleen	Spleen
7	chr16:75268200-75277000	Strong transcription	H9 Cell Line	embryonic stem cell
8	chr16:75268400-75275600	Weak transcription	GM12878-XiMat	blood
9	chr16:75268600-75277800	Strong transcription	Sigmoid Colon	Sigmoid Colon
10	chr16:75268800-75275000	Weak transcription	K562	blood
11	chr16:75269600-75280600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr16:75269800-75274800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr16:75270400-75278400	Genic enhancers	Fetal Muscle Leg	muscle
14	chr16:75270400-75278800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr16:75270600-75274800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr16:75271000-75275000	Enhancers	Brain Substantia Nigra	brain
17	chr16:75271000-75275400	Genic enhancers	Fetal Stomach	stomach
18	chr16:75271200-75274200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr16:75271200-75274800	Enhancers	Left Ventricle	heart
20	chr16:75271200-75275000	Enhancers	Fetal Brain Male	brain
21	chr16:75271200-75278000	Genic enhancers	Fetal Muscle Trunk	muscle
22	chr16:75271400-75275200	Enhancers	Right Atrium	heart
23	chr16:75271600-75274200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr16:75271600-75274200	Genic enhancers	Placenta	Placenta
25	chr16:75271600-75274200	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr16:75271600-75274400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr16:75271600-75274400	Enhancers	HMEC	breast
28	chr16:75271600-75274800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr16:75271600-75275400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr16:75271800-75274200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr16:75271800-75274200	Enhancers	Psoas Muscle	Psoas
32	chr16:75271800-75274400	Genic enhancers	Colonic Mucosa	Colon
33	chr16:75271800-75274400	Genic enhancers	Osteobl	bone
34	chr16:75271800-75278200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr16:75272000-75274400	Genic enhancers	A549	lung
36	chr16:75272200-75274200	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr16:75272200-75274600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr16:75272200-75275200	Genic enhancers	Lung	lung
39	chr16:75272400-75274800	Enhancers	Fetal Heart	heart
40	chr16:75272400-75276200	Genic enhancers	HUVEC	blood vessel
41	chr16:75272600-75274400	Genic enhancers	Duodenum Smooth Muscle	Duodenum
42	chr16:75272800-75274400	Enhancers	NHEK	skin
43	chr16:75272800-75278800	Genic enhancers	Gastric	stomach
44	chr16:75273000-75274200	Transcr. at gene 5' and 3'	HepG2	liver
45	chr16:75273000-75277200	Genic enhancers	Right Ventricle	heart
46	chr16:75273200-75274400	Enhancers	HSMM	muscle
47	chr16:75273200-75274800	Enhancers	Brain Anterior Caudate	brain
48	chr16:75273200-75275800	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr16:75273200-75275800	Genic enhancers	NH-A	brain
50	chr16:75273200-75276000	Genic enhancers	Muscle Satellite Cultured Cells	--

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