Variant report

Variant	esv2596575
Chromosome Location	chr13:76109159-76111338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr13:76111165-76112724	IMR90	lung:	n/a	n/a
2	CTCF	chr13:76109140-76109290	AG04450	lung:	n/a	n/a
3	CTCF	chr13:76109340-76109490	AG04450	lung:	n/a	n/a
4	CTCF	chr13:76110840-76110990	AG04450	lung:	n/a	n/a
5	CTCF	chr13:76110600-76110750	AG04450	lung:	n/a	n/a
6	CUX1	chr13:76111274-76111283	GM12878	blood:	n/a	n/a
7	MAX	chr13:76111330-76112655	ECC-1	luminal epithelium:	n/a	chr13:76112223-76112242 chr13:76112409-76112419
8	MTA3	chr13:76111314-76112575	GM12878	blood:	n/a	n/a
9	MXI1	chr13:76110556-76112811	SK-N-SH	brain:	n/a	n/a
10	MYC	chr13:76111042-76111220	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr13:76111310-76112714	U87	brain:	n/a	n/a
12	POLR2A	chr13:76109552-76109837	HepG2	liver:	n/a	n/a
13	POLR2A	chr13:76110429-76110563	MCF10A-Er-Src	breast:	n/a	n/a
14	POLR2A	chr13:76108945-76109200	MCF10A-Er-Src	breast:	n/a	n/a
15	POLR2A	chr13:76111117-76111232	HUVEC	blood vessel:	n/a	n/a
16	POLR2A	chr13:76110668-76110868	MCF10A-Er-Src	breast:	n/a	n/a
17	POLR2A	chr13:76109564-76109590	K562	blood:	n/a	n/a
18	POLR2A	chr13:76109131-76109808	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr13:76111249-76111343	HUVEC	blood vessel:	n/a	n/a
20	POLR2A	chr13:76109758-76109786	K562	blood:	n/a	n/a
21	POLR2A	chr13:76111189-76112572	GM12878	blood:	n/a	n/a
22	POLR2A	chr13:76109726-76109732	K562	blood:	n/a	n/a
23	POLR2A	chr13:76109316-76109486	K562	blood:	n/a	n/a
24	POLR2A	chr13:76109464-76109549	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr13:76109797-76109912	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr13:76109475-76109602	ProgFib	skin:	n/a	n/a
27	POLR2A	chr13:76109202-76109963	K562	blood:	n/a	n/a
28	POLR2A	chr13:76111197-76111217	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr13:76110953-76112822	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr13:76111297-76112797	GM18505	blood:	n/a	n/a
31	POLR2A	chr13:76109568-76109641	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr13:76109310-76109751	GM12878	blood:	n/a	n/a
33	POLR2A	chr13:76108550-76110007	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr13:76111155-76111190	HepG2	liver:	n/a	n/a
35	POLR2A	chr13:76111023-76112653	GM12891	blood:	n/a	n/a
36	POLR2A	chr13:76109614-76109622	ProgFib	skin:	n/a	n/a
37	POLR2A	chr13:76111143-76111154	K562	blood:	n/a	n/a
38	RFX5	chr13:76111218-76112582	Hela-S3	cervix:	n/a	n/a
39	SREBP1	chr13:76110890-76113428	GM12878	blood:	n/a	n/a
40	WRNIP1	chr13:76111057-76111215	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76111107-76111157	HRE	kidney:	n/a
2	chr13:76111107-76111157	GM12878	blood:	n/a
3	chr13:76111107-76111157	HepG2	liver:	n/a
4	chr13:76109220-76109270	RPTEC	kidney:	n/a
5	chr13:76111107-76111157	PANC-1	pancreas:	n/a
6	chr13:76111107-76111157	IMR90	lung:	fetal
7	chr13:76109220-76109270	HepG2	liver:	n/a
8	chr13:76111107-76111157	MCF-7	breast:	n/a
9	chr13:76111107-76111157	ProgFib	skin:	n/a
10	chr13:76111107-76111157	SK-N-SH	brain:	n/a
11	chr13:76111107-76111157	NHBE	bronchial:	n/a
12	chr13:76109220-76109270	NB4	blood:	n/a
13	chr13:76111107-76111157	HNPCEpiC	eye:	n/a
14	chr13:76109220-76109270	PFSK-1	brain:	n/a
15	chr13:76111107-76111157	BJ	skin:	n/a
16	chr13:76109220-76109270	Hela-S3	cervix:	n/a
17	chr13:76111107-76111157	RPTEC	kidney:	n/a
18	chr13:76111107-76111157	HCT-116	colon:	n/a
19	chr13:76111107-76111157	NT2-D1	testis:	n/a
20	chr13:76111107-76111157	HUVEC	blood vessel:	n/a
21	chr13:76109220-76109270	BJ	skin:	n/a
22	chr13:76109220-76109270	GM12878	blood:	n/a
23	chr13:76111107-76111157	NH-A	brain:	n/a
24	chr13:76111107-76111157	LNCaP	prostate:	n/a
25	chr13:76111107-76111157	GM12892	blood:	n/a
26	chr13:76109220-76109270	HRPEpiC	eye:	n/a
27	chr13:76109220-76109270	CMK	blood:	n/a
28	chr13:76109220-76109270	SK-N-SH	brain:	n/a
29	chr13:76111107-76111157	AG09319	gingival:	n/a
30	chr13:76109220-76109270	AG09319	gingival:	n/a
31	chr13:76109220-76109270	K562	blood:	n/a
32	chr13:76109220-76109270	SKMC	muscle:	n/a
33	chr13:76111107-76111157	NHDF-neo	bronchial:	n/a
34	chr13:76109220-76109270	GM06990	blood:	n/a
35	chr13:76109220-76109270	T-47D	breast:	n/a
36	chr13:76109220-76109270	Caco-2	colon:	n/a
37	chr13:76111107-76111157	SK-N-SH_RA	brain:	n/a
38	chr13:76109220-76109270	HPAEpiC	pulmonary alveolar:	n/a
39	chr13:76109220-76109270	HL-60	blood:	n/a
40	chr13:76109220-76109270	ovcar-3	ovarian:	n/a
41	chr13:76109220-76109270	ProgFib	skin:	n/a
42	chr13:76111107-76111157	Caco-2	colon:	n/a
43	chr13:76109220-76109270	A549	lung:	n/a
44	chr13:76111107-76111157	AoSMC	blood vessel:	n/a
45	chr13:76111107-76111157	A549	lung:	n/a
46	chr13:76111107-76111157	U87	brain:	n/a
47	chr13:76109220-76109270	HCPEpiC	choroid plexus:	n/a
48	chr13:76109220-76109270	NHDF-neo	bronchial:	n/a
49	chr13:76109220-76109270	PrEC	prostate:	n/a
50	chr13:76111107-76111157	H1-hESC	embryonic stem cell:	embryo

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:76107791..76110428-chr13:76144234..76145882,2	K562	blood:
2	chr13:76106394..76109955-chr13:76110419..76113939,6	MCF-7	breast:
3	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
4	chr13:76055248..76057886-chr13:76110224..76112780,4	MCF-7	breast:
5	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:
6	chr13:76109717..76113590-chr13:76122029..76126081,5	MCF-7	breast:
7	chr13:76055919..76057695-chr13:76110507..76112437,2	MCF-7	breast:
8	chr13:76101020..76103303-chr13:76108939..76111291,2	K562	blood:
9	chr13:76101122..76104303-chr13:76108576..76110569,3	K562	blood:
10	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:

No data

Variant related genes	Relation type
COMMD6	TF binding region
COMMD6	CpG island
ENSG00000188243	chromatin interactions
ENSG00000118939	chromatin interactions
ENSG00000261553	chromatin interactions
ENSG00000136111	chromatin interactions

Extended variants
information (count: 74 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141122316	chr13:76109198-76109199	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs9600489	chr13:76109221-76109222	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563628730	chr13:76109258-76109259	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs375747095	chr13:76109261-76109262	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs4885309	chr13:76109285-76109286	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs201363947	chr13:76109289-76109290	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs576241355	chr13:76109290-76109291	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs55887720	chr13:76109292-76109293	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs201959512	chr13:76109293-76109294	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs398056568	chr13:76109294-76109295	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548391591	chr13:76109352-76109353	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs545635399	chr13:76109366-76109367	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs150268116	chr13:76109398-76109399	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs138921578	chr13:76109424-76109425	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs140664266	chr13:76109476-76109477	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs145764226	chr13:76109486-76109487	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs530142432	chr13:76109495-76109496	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs187009148	chr13:76109534-76109535	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs7985488	chr13:76109536-76109537	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs190218707	chr13:76109558-76109559	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs552811575	chr13:76109589-76109590	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs570608255	chr13:76109591-76109592	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570536431	chr13:76109611-76109612	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs534725295	chr13:76109612-76109613	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs553069463	chr13:76109613-76109614	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs574332786	chr13:76109697-76109698	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs535480483	chr13:76109755-76109756	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs537607915	chr13:76109766-76109767	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs577121626	chr13:76109789-76109790	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs375025266	chr13:76109804-76109805	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs575183661	chr13:76109815-76109816	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs6562905	chr13:76109836-76109837	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs563961357	chr13:76109932-76109933	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs576892679	chr13:76109933-76109934	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs182767865	chr13:76109958-76109959	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs559822159	chr13:76110003-76110004	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs568115429	chr13:76110024-76110025	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs534221177	chr13:76110028-76110029	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs187649166	chr13:76110202-76110203	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs137957924	chr13:76110215-76110216	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs115613540	chr13:76110306-76110307	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs535452395	chr13:76110338-76110339	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs553793366	chr13:76110349-76110350	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs193224549	chr13:76110364-76110365	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs571044859	chr13:76110378-76110379	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs535264567	chr13:76110382-76110383	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs572697572	chr13:76110383-76110384	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs568188264	chr13:76110396-76110397	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs535067283	chr13:76110470-76110471	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs142435984	chr13:76110473-76110474	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76093600-76109400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr13:76095600-76109200	Weak transcription	Gastric	stomach
3	chr13:76095800-76111400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr13:76096600-76110400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr13:76096600-76111400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:76097000-76111000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr13:76097000-76111600	Weak transcription	Spleen	Spleen
8	chr13:76097800-76110400	Weak transcription	Brain Angular Gyrus	brain
9	chr13:76097800-76110600	Weak transcription	Fetal Brain Male	brain
10	chr13:76097800-76110600	Weak transcription	Fetal Kidney	kidney
11	chr13:76097800-76110600	Weak transcription	Psoas Muscle	Psoas
12	chr13:76097800-76111200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr13:76098000-76110400	Weak transcription	A549	lung
14	chr13:76098000-76110400	Weak transcription	HUVEC	blood vessel
15	chr13:76098000-76110600	Weak transcription	Brain Anterior Caudate	brain
16	chr13:76098000-76110600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr13:76098000-76111200	Weak transcription	Aorta	Aorta
18	chr13:76098200-76109600	Weak transcription	Brain Germinal Matrix	brain
19	chr13:76098200-76110400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr13:76098400-76110200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr13:76098600-76111000	Weak transcription	Colonic Mucosa	Colon
22	chr13:76098800-76110400	Weak transcription	Brain Cingulate Gyrus	brain
23	chr13:76098800-76111400	Weak transcription	Esophagus	oesophagus
24	chr13:76099400-76109400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr13:76099400-76110400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:76099600-76109400	Weak transcription	HSMMtube	muscle
27	chr13:76099600-76110200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr13:76099600-76111000	Weak transcription	K562	blood
29	chr13:76100000-76109200	Weak transcription	Lung	lung
30	chr13:76100000-76109400	Weak transcription	Left Ventricle	heart
31	chr13:76100000-76109400	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr13:76100000-76110600	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr13:76100000-76111200	Weak transcription	Ovary	ovary
34	chr13:76100200-76109200	Weak transcription	Colon Smooth Muscle	Colon
35	chr13:76100200-76109200	Weak transcription	Thymus	Thymus
36	chr13:76100200-76110400	Weak transcription	Brain Substantia Nigra	brain
37	chr13:76100200-76110600	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr13:76100400-76110600	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr13:76100600-76109400	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr13:76100800-76110000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr13:76100800-76110600	Weak transcription	Right Ventricle	heart
42	chr13:76101200-76109200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr13:76102200-76110400	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr13:76103600-76111000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr13:76104000-76110600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr13:76104200-76109400	Weak transcription	Pancreas	Pancrea
47	chr13:76104400-76110400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr13:76105000-76109200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr13:76105000-76110600	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr13:76105000-76111200	Weak transcription	Stomach Mucosa	stomach

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