Variant report

Variant	nsv899962
Chromosome Location	chr13:30831422-30863235
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:135)
CpG islands
(count:245)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:135 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr13:30850346-30850625	GM12878	blood:	n/a	n/a
2	BCL11A	chr13:30850345-30850545	GM12878	blood:	n/a	n/a
3	CEBPB	chr13:30846978-30847241	K562	blood:	n/a	chr13:30847055-30847066
4	CEBPB	chr13:30847008-30847190	HepG2	liver:	n/a	chr13:30847055-30847066
5	CEBPB	chr13:30853906-30853918	IMR90	lung:	n/a	n/a
6	CEBPB	chr13:30845930-30846130	K562	blood:	n/a	chr13:30846040-30846051 chr13:30846040-30846053
7	CTCF	chr13:30860874-30860876	MCF-7	breast:	n/a	n/a
8	CTCF	chr13:30860680-30860830	Caco-2	colon:	n/a	n/a
9	CTCF	chr13:30854135-30854204	GM20000	blood:	n/a	n/a
10	CTCF	chr13:30860771-30860791	MCF-7	breast:	n/a	n/a
11	CTCF	chr13:30860884-30860894	MCF-7	breast:	n/a	n/a
12	CTCF	chr13:30860720-30860870	HEK293	kidney:	n/a	n/a
13	CTCF	chr13:30860760-30860910	HepG2	liver:	n/a	n/a
14	CTCF	chr13:30831619-30831680	MCF-7	breast:	n/a	n/a
15	CTCF	chr13:30860741-30860956	MCF-7	breast:	n/a	n/a
16	CTCF	chr13:30860720-30860870	GM12873	blood:	n/a	n/a
17	CTCF	chr13:30860780-30860930	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr13:30860740-30860890	BE2_C	brain:	n/a	n/a
19	CTCF	chr13:30859520-30859670	RPTEC	kidney:	n/a	n/a
20	CTCF	chr13:30860740-30860890	GM12871	blood:	n/a	n/a
21	CTCF	chr13:30831820-30831970	GM12865	blood:	n/a	n/a
22	CTCF	chr13:30833382-30833409	Fibrobl	skin:	n/a	n/a
23	CTCF	chr13:30860700-30860850	SAEC	small airway:	n/a	n/a
24	CTCF	chr13:30831680-30831830	GM12867	blood:	n/a	n/a
25	CTCF	chr13:30860720-30860870	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr13:30860727-30860808	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr13:30831658-30831708	MCF-7	breast:	n/a	n/a
28	CTCF	chr13:30860913-30860977	MCF-7	breast:	n/a	n/a
29	CTCF	chr13:30860720-30860870	BE2_C	brain:	n/a	n/a
30	CTCF	chr13:30831672-30831674	MCF-7	breast:	n/a	n/a
31	CTCF	chr13:30830943-30831495	K562	blood:	n/a	n/a
32	CTCF	chr13:30860482-30860570	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr13:30860748-30860861	MCF-7	breast:	n/a	n/a
34	CTCF	chr13:30831616-30831618	MCF-7	breast:	n/a	n/a
35	CTCF	chr13:30860744-30860946	MCF-7	breast:	n/a	n/a
36	CTCF	chr13:30860720-30860870	GM12872	blood:	n/a	n/a
37	CTCF	chr13:30860902-30860960	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:30860720-30860870	GM12867	blood:	n/a	n/a
39	E2F4	chr13:30846841-30846878	MCF10A-Er-Src	breast:	n/a	n/a
40	EBF1	chr13:30850460-30850565	GM12878	blood:	n/a	n/a
41	ELK1	chr13:30831924-30831926	GM12878	blood:	n/a	n/a
42	EP300	chr13:30831890-30832273	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr13:30831931-30832246	SK-N-SH_RA	brain:	n/a	n/a
44	FOS	chr13:30857646-30858010	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr13:30857644-30858032	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr13:30857690-30857941	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr13:30857634-30858008	MCF10A-Er-Src	breast:	n/a	n/a
48	FOXA1	chr13:30862864-30863089	HepG2	liver:	n/a	n/a
49	FOXA1	chr13:30862864-30863186	HepG2	liver:	n/a	n/a
50	FOXA1	chr13:30862862-30863132	T-47D	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:30843564-30843614	GM12878	blood:	n/a
2	chr13:30843564-30843614	GM12878	blood:	n/a
3	chr13:30843564-30843614	HL-60	blood:	n/a
4	chr13:30841291-30841341	AG04449	skin:	fetal
5	chr13:30831499-30831549	HCT-116	colon:	n/a
6	chr13:30843564-30843614	GM12892	blood:	n/a
7	chr13:30843564-30843614	BJ	skin:	n/a
8	chr13:30833766-30833816	LNCaP	prostate:	n/a
9	chr13:30831499-30831549	GM19239	blood:	n/a
10	chr13:30831499-30831549	BE2_C	brain:	n/a
11	chr13:30831499-30831549	GM12878	blood:	n/a
12	chr13:30843564-30843614	RPTEC	kidney:	n/a
13	chr13:30841291-30841341	AoSMC	blood vessel:	n/a
14	chr13:30833766-30833816	ProgFib	skin:	n/a
15	chr13:30841291-30841341	BE2_C	brain:	n/a
16	chr13:30831499-30831549	HAEpiC	amniotic membrane:	n/a
17	chr13:30831499-30831549	AG04450	lung:	fetal
18	chr13:30831499-30831549	HCPEpiC	choroid plexus:	n/a
19	chr13:30841291-30841341	HCM	heart:	n/a
20	chr13:30833766-30833816	U87	brain:	n/a
21	chr13:30831499-30831549	NB4	blood:	n/a
22	chr13:30833766-30833816	HCF	heart:	n/a
23	chr13:30833766-30833816	RPTEC	kidney:	n/a
24	chr13:30841291-30841341	HCT-116	colon:	n/a
25	chr13:30841291-30841341	HRCEpiC	kidney:	n/a
26	chr13:30841291-30841341	NHDF-neo	bronchial:	n/a
27	chr13:30833766-30833816	HCM	heart:	n/a
28	chr13:30841291-30841341	HAEpiC	amniotic membrane:	n/a
29	chr13:30833766-30833816	Hepatocyte	liver:	n/a
30	chr13:30843564-30843614	HIPEpiC	eye:	n/a
31	chr13:30843564-30843614	T-47D	breast:	n/a
32	chr13:30833766-30833816	AG10803	skin:	n/a
33	chr13:30831499-30831549	HCM	heart:	n/a
34	chr13:30841291-30841341	Caco-2	colon:	n/a
35	chr13:30831499-30831549	PANC-1	pancreas:	n/a
36	chr13:30833766-30833816	BE2_C	brain:	n/a
37	chr13:30833766-30833816	HIPEpiC	eye:	n/a
38	chr13:30831499-30831549	RPTEC	kidney:	n/a
39	chr13:30841291-30841341	HCF	heart:	n/a
40	chr13:30833766-30833816	HRPEpiC	eye:	n/a
41	chr13:30841291-30841341	HMEC	breast:	n/a
42	chr13:30841291-30841341	GM19239	blood:	n/a
43	chr13:30841291-30841341	HUVEC	blood vessel:	n/a
44	chr13:30831499-30831549	MCF-7	breast:	n/a
45	chr13:30841291-30841341	Hela-S3	cervix:	n/a
46	chr13:30843564-30843614	HCF	heart:	n/a
47	chr13:30831499-30831549	ProgFib	skin:	n/a
48	chr13:30841291-30841341	NH-A	brain:	n/a
49	chr13:30831499-30831549	HEEpiC	esophagus:	n/a
50	chr13:30841291-30841341	SKMC	muscle:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:30845289..30847410-chr13:30848060..30849605,2	K562	blood:
2	chr13:30859379..30862261-chr13:30868087..30870616,3	K562	blood:
3	chr13:30830170..30831527-chr13:30908713..30909751,4	MCF-7	breast:
4	chr13:30856428..30858941-chr13:31030310..31031836,2	K562	blood:
5	chr13:30859379..30862261-chr13:30868087..30870616,2	K562	blood:
6	chr13:30859194..30861688-chr13:30861756..30863782,2	K562	blood:
7	chr13:30845289..30847410-chr13:30848060..30849605,2	K562	blood:
8	chr13:30861210..30864366-chr13:30881406..30883118,3	K562	blood:
9	chr13:30839724..30842473-chr19:16111566..16113469,2	MCF-7	breast:
10	chr13:30859194..30861688-chr13:30861756..30863782,2	K562	blood:
11	chr13:30708914..30710508-chr13:30839342..30841518,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-64P	TF binding region
RNU6-64P	CpG island
ENSG00000102781	chromatin interactions
ENSG00000215049	chromatin interactions

Extended variants
information (count: 1223 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1054438	chr13:30831422-30831423	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35905181	chr13:30831426-30831427	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs149660234	chr13:30831499-30831500	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs9508685	chr13:30831531-30831532	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs564140544	chr13:30831532-30831533	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs532803709	chr13:30831552-30831553	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs546544961	chr13:30831554-30831555	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs566244527	chr13:30831572-30831573	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs114330398	chr13:30831607-30831608	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs146674667	chr13:30831642-30831643	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs369756733	chr13:30831644-30831645	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs568294761	chr13:30831648-30831649	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs183785079	chr13:30831655-30831656	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs73163477	chr13:30831672-30831673	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs142124589	chr13:30831697-30831698	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs3041575	chr13:30831701-30831702	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs557192070	chr13:30831705-30831706	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs577242235	chr13:30831732-30831733	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs145606198	chr13:30831755-30831756	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs375596142	chr13:30831785-30831786	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs548275137	chr13:30831786-30831787	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs569818166	chr13:30831801-30831802	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs573095957	chr13:30831804-30831805	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs537008239	chr13:30831827-30831828	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs542140446	chr13:30831859-30831860	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs368211858	chr13:30831865-30831866	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs189196883	chr13:30831873-30831874	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs544385238	chr13:30831878-30831879	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs570164252	chr13:30831893-30831894	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs74627875	chr13:30831933-30831934	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs191402204	chr13:30831938-30831939	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs546321890	chr13:30831954-30831955	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs560093763	chr13:30832005-30832006	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs182493587	chr13:30832018-30832019	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs186811513	chr13:30832124-30832125	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs191650567	chr13:30832200-30832201	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs184963765	chr13:30832201-30832202	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73163478	chr13:30832315-30832316	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs55791170	chr13:30832375-30832376	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs673477	chr13:30832417-30832418	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs604061	chr13:30832418-30832419	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs189896000	chr13:30832512-30832513	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs137973596	chr13:30832513-30832514	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74043068	chr13:30832515-30832516	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs149087823	chr13:30832631-30832632	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544420804	chr13:30832648-30832649	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557891006	chr13:30832660-30832661	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577713907	chr13:30832694-30832695	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540303921	chr13:30832723-30832724	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559929560	chr13:30832760-30832761	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Squamous cell cancer	20885788	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Malignant glioma	17146433	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Retinoblastoma	22278416	CNVD
Peters Plus syndrome	16909395	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Ovarian cancer	19047089	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30799400-30831600	Weak transcription	Right Ventricle	heart
2	chr13:30799600-30845200	Weak transcription	HMEC	breast
3	chr13:30804400-30831600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr13:30805600-30831600	Weak transcription	Left Ventricle	heart
5	chr13:30805600-30831600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr13:30805600-30841800	Weak transcription	Ovary	ovary
7	chr13:30805600-30853200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr13:30810000-30831600	Weak transcription	NHLF	lung
9	chr13:30810600-30849200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr13:30813000-30849000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr13:30820600-30831800	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr13:30820600-30831800	Weak transcription	HSMMtube	muscle
13	chr13:30822400-30833600	Weak transcription	K562	blood
14	chr13:30822800-30834000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr13:30823400-30831600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr13:30823600-30831600	Weak transcription	Fetal Brain Male	brain
17	chr13:30823600-30849200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr13:30823600-30849200	Weak transcription	HSMM	muscle
19	chr13:30823800-30833800	Weak transcription	NHEK	skin
20	chr13:30823800-30849200	Weak transcription	Fetal Brain Female	brain
21	chr13:30824000-30831600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr13:30824000-30831600	Weak transcription	Primary B cells from peripheral blood	blood
23	chr13:30824000-30831600	Weak transcription	Adipose Nuclei	Adipose
24	chr13:30824000-30831600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr13:30824000-30832000	Weak transcription	Fetal Kidney	kidney
26	chr13:30824000-30832000	Weak transcription	Osteobl	bone
27	chr13:30824000-30833400	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr13:30824000-30845200	Weak transcription	Thymus	Thymus
29	chr13:30824000-30848800	Weak transcription	Fetal Muscle Leg	muscle
30	chr13:30824200-30849200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr13:30824400-30831600	Weak transcription	Primary B cells from cord blood	blood
32	chr13:30824400-30831800	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr13:30824400-30849200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr13:30824600-30833400	Weak transcription	Pancreas	Pancrea
35	chr13:30824800-30832800	Strong transcription	Dnd41	blood
36	chr13:30825000-30831800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:30825000-30831800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr13:30825800-30831600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr13:30825800-30831600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr13:30826800-30860400	Weak transcription	Esophagus	oesophagus
41	chr13:30827200-30831600	Weak transcription	Gastric	stomach
42	chr13:30827400-30833600	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr13:30828200-30831800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr13:30828200-30833400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr13:30828200-30837000	Weak transcription	HUVEC	blood vessel
46	chr13:30828200-30849000	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr13:30828400-30831600	Weak transcription	Lung	lung
48	chr13:30828400-30848800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr13:30828600-30857600	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr13:30829200-30831600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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