Variant report

Variant	nsv900587
Chromosome Location	chr13:79894736-79956691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:246)
CpG islands
(count:0)
Chromatin interactive
region (count:42)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:79956555-79957101	GM12878	blood:	n/a	n/a
2	BHLHE40	chr13:79911736-79911875	GM12878	blood:	n/a	n/a
3	BHLHE40	chr13:79934271-79934541	GM12878	blood:	n/a	n/a
4	CCNT2	chr13:79937924-79938001	K562	blood:	n/a	n/a
5	CEBPB	chr13:79942751-79943084	IMR90	lung:	n/a	n/a
6	CEBPB	chr13:79923157-79923479	HepG2	liver:	n/a	n/a
7	CEBPB	chr13:79923159-79923511	IMR90	lung:	n/a	n/a
8	CEBPB	chr13:79953297-79953497	H1-hESC	embryonic stem cell:	n/a	chr13:79953363-79953376 chr13:79953363-79953374 chr13:79953363-79953374 chr13:79953363-79953376
9	CEBPB	chr13:79942740-79943056	K562	blood:	n/a	n/a
10	CEBPB	chr13:79939205-79939323	A549	lung:	n/a	n/a
11	CEBPB	chr13:79952098-79952407	IMR90	lung:	n/a	n/a
12	CEBPB	chr13:79923157-79923437	K562	blood:	n/a	n/a
13	CEBPB	chr13:79923193-79923449	A549	lung:	n/a	n/a
14	CEBPB	chr13:79942742-79943079	HepG2	liver:	n/a	n/a
15	CHD1	chr13:79934607-79934654	GM12878	blood:	n/a	n/a
16	CTCF	chr13:79908701-79908773	K562	blood:	n/a	n/a
17	CTCF	chr13:79923880-79923946	MCF-7	breast:	n/a	n/a
18	CTCF	chr13:79914739-79914906	Medullo	brain:	n/a	chr13:79914815-79914833 chr13:79914810-79914831
19	CTCF	chr13:79914681-79914881	K562	blood:	n/a	chr13:79914815-79914833 chr13:79914810-79914831
20	CTCF	chr13:79914740-79914890	Caco-2	colon:	n/a	chr13:79914815-79914833 chr13:79914810-79914831
21	CTCF	chr13:79914809-79914892	Hela-S3	cervix:	n/a	chr13:79914815-79914833 chr13:79914810-79914831
22	CTCF	chr13:79914660-79914810	HMEC	breast:	n/a	n/a
23	CTCF	chr13:79914807-79914864	GM13977	blood:	n/a	chr13:79914815-79914833 chr13:79914810-79914831
24	CTCF	chr13:79946558-79946614	Lung_OC	lung:	n/a	n/a
25	CTCF	chr13:79914840-79914990	GM06990	blood:	n/a	n/a
26	CTCF	chr13:79914726-79914936	GM12878	blood:	n/a	chr13:79914815-79914833 chr13:79914810-79914831
27	CTCF	chr13:79921240-79921390	Caco-2	colon:	n/a	n/a
28	CTCF	chr13:79914813-79914849	HUVEC	blood vessel:	n/a	chr13:79914815-79914833
29	CTCF	chr13:79951220-79951370	GM12864	blood:	n/a	n/a
30	CTCF	chr13:79914660-79914810	HMF	breast:	n/a	n/a
31	CTCF	chr13:79923875-79923952	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr13:79914720-79914870	HPAF	blood vessel:	n/a	chr13:79914815-79914833 chr13:79914810-79914831
33	CTCF	chr13:79914720-79914870	HCPEpiC	choroid plexus:	n/a	chr13:79914815-79914833 chr13:79914810-79914831
34	CTCF	chr13:79914620-79914910	HPAF	blood vessel:	n/a	chr13:79914815-79914833 chr13:79914810-79914831
35	CTCF	chr13:79894993-79895263	GM12878	blood:	n/a	chr13:79895117-79895133 chr13:79895111-79895132
36	CTCF	chr13:79895011-79895233	K562	blood:	n/a	chr13:79895117-79895133 chr13:79895111-79895132
37	CTCF	chr13:79895077-79895177	LNCaP	prostate:	n/a	chr13:79895117-79895133 chr13:79895111-79895132
38	CTCF	chr13:79914805-79914831	GM10248	blood:	n/a	chr13:79914810-79914831
39	E2F4	chr13:79922318-79922700	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr13:79904851-79905054	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr13:79894971-79895209	MCF10A-Er-Src	breast:	n/a	n/a
42	EBF1	chr13:79934301-79934482	GM12878	blood:	n/a	n/a
43	EBF1	chr13:79937887-79938096	GM12878	blood:	n/a	n/a
44	EP300	chr13:79948749-79949064	SK-N-SH_RA	brain:	n/a	chr13:79949026-79949034 chr13:79949013-79949022
45	EP300	chr13:79914579-79914621	K562	blood:	n/a	n/a
46	EP300	chr13:79956624-79957009	GM12878	blood:	n/a	n/a
47	EP300	chr13:79956647-79957086	GM12878	blood:	n/a	n/a
48	EP300	chr13:79948754-79949119	SK-N-SH_RA	brain:	n/a	chr13:79949026-79949034 chr13:79949013-79949022
49	FAM48A	chr13:79909228-79909328	GM12878	blood:	n/a	n/a
50	FOS	chr13:79952025-79952377	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:79945909..79948690-chr13:79954494..79956111,2	K562	blood:
2	chr13:79944448..79946891-chr13:79951431..79952941,2	MCF-7	breast:
3	chr13:79954344..79956501-chr13:79980394..79983351,2	K562	blood:
4	chr13:79902131..79904389-chr13:79920319..79922691,2	K562	blood:
5	chr13:79923102..79925084-chr13:79942134..79944887,2	K562	blood:
6	chr13:79920827..79922922-chr13:79926144..79928046,2	K562	blood:
7	chr11:10962597..10964101-chr13:79936577..79938077,2	MCF-7	breast:
8	chr13:79936577..79938077-chr17:41464201..41465745,3	K562	blood:
9	chr13:79920013..79921997-chr13:80113156..80114886,2	K562	blood:
10	chr13:79955549..79959842-chr13:79960157..79964525,5	K562	blood:
11	chr13:79949599..79952196-chr13:79952823..79955805,2	MCF-7	breast:
12	chr13:79936577..79938077-chr17:41464201..41466223,4	K562	blood:
13	chr13:79936577..79938077-chr3:73159867..73161607,3	K562	blood:
14	chr13:79920827..79922922-chr13:79926144..79928046,2	K562	blood:
15	chr13:79915442..79917474-chr13:79934906..79936964,2	K562	blood:
16	chr13:79936557..79938077-chr17:41464180..41465889,2	MCF-7	breast:
17	chr13:79887279..79889348-chr13:79896900..79898498,2	K562	blood:
18	chr13:79929694..79931725-chr13:79939239..79940753,2	K562	blood:
19	chr11:62608635..62609629-chr13:79936557..79937077,5	HCT-116	colon:
20	chr13:79936577..79937077-chr17:41465207..41466163,2	HCT-116	colon:
21	chr13:79919488..79921002-chr13:79921082..79922938,2	K562	blood:
22	chr13:79929694..79931725-chr13:79939239..79940753,2	K562	blood:
23	chr13:79936577..79938077-chr17:41463333..41465885,2	MCF-7	breast:
24	chr13:79914794..79916767-chr13:79918127..79921479,3	K562	blood:
25	chr13:79955154..79956833-chr13:79959758..79961618,3	MCF-7	breast:
26	chr13:79945909..79948690-chr13:79954494..79956111,2	K562	blood:
27	chr13:79936404..79939084-chr13:79941212..79942722,2	K562	blood:
28	chr13:79944448..79946891-chr13:79951431..79952941,2	MCF-7	breast:
29	chr13:79919488..79921002-chr13:79921082..79922938,2	K562	blood:
30	chr13:79887290..79888796-chr13:79894827..79897336,2	MCF-7	breast:
31	chr13:79936577..79938077-chr3:73158465..73161432,2	K562	blood:
32	chr11:62607642..62610723-chr13:79936557..79938077,5	K562	blood:
33	chr13:79936077..79937077-chr3:73160028..73160608,4	HCT-116	colon:
34	chr13:79940489..79942669-chr13:79947874..79950241,2	MCF-7	breast:
35	chr13:79923102..79925084-chr13:79942134..79944887,2	K562	blood:
36	chr13:79936577..79937077-chr3:73160028..73160610,2	MCF-7	breast:
37	chr13:79902131..79904389-chr13:79920319..79922691,2	K562	blood:
38	chr13:79904552..79907167-chr7:5465284..5467167,2	MCF-7	breast:
39	chr13:79915442..79917474-chr13:79934906..79936964,2	K562	blood:
40	chr13:79936404..79939084-chr13:79941212..79942722,2	K562	blood:
41	chr13:79938020..79940592-chr13:79963302..79965258,2	K562	blood:
42	chr13:79949599..79952196-chr13:79952823..79955805,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF219-3	chr13:79923725-79924372	ENSG00000250925

No data

Variant related genes	Relation type
RBM26	TF binding region
ENSG00000227354	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000252496	chromatin interactions
ENSG00000272953	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000139746	chromatin interactions
ENSG00000223247	chromatin interactions
SLC35F3	miRNA target sites

Extended variants
information (count: 2442 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2442 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3187338	chr13:79894736-79894737	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533973256	chr13:79894781-79894782	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146868835	chr13:79894795-79894796	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34668220	chr13:79894877-79894878	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543274311	chr13:79894878-79894879	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs386379883	chr13:79894884-79894885	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs386379884	chr13:79894885-79894886	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376804738	chr13:79894891-79894892	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547346472	chr13:79894930-79894931	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183590766	chr13:79894951-79894952	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571688740	chr13:79894970-79894971	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186471611	chr13:79895035-79895036	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112708297	chr13:79895046-79895047	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576595136	chr13:79895051-79895052	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539217109	chr13:79895080-79895081	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191508852	chr13:79895153-79895154	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577769737	chr13:79895183-79895184	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540233754	chr13:79895325-79895326	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556484687	chr13:79895336-79895337	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200926684	chr13:79895437-79895438	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539017996	chr13:79895627-79895628	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573999962	chr13:79895653-79895654	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182412688	chr13:79895683-79895684	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557102275	chr13:79895695-79895696	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186685459	chr13:79895744-79895745	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191094552	chr13:79895806-79895807	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551546054	chr13:79895853-79895854	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183449636	chr13:79895873-79895874	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527732801	chr13:79895956-79895957	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369096013	chr13:79895975-79895976	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373831652	chr13:79895991-79895992	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567291521	chr13:79896100-79896101	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148449537	chr13:79896102-79896103	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550237139	chr13:79896145-79896146	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs80185968	chr13:79896233-79896234	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142739898	chr13:79896257-79896258	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559059423	chr13:79896309-79896310	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571387221	chr13:79896311-79896312	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151007243	chr13:79896409-79896410	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536960813	chr13:79896424-79896425	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371997110	chr13:79896432-79896433	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7983606	chr13:79896445-79896446	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs373873847	chr13:79896467-79896468	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549107895	chr13:79896476-79896477	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140824394	chr13:79896507-79896508	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576246905	chr13:79896518-79896519	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544879685	chr13:79896556-79896557	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375023858	chr13:79896565-79896566	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564713136	chr13:79896611-79896612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527797753	chr13:79896667-79896668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
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	21098271	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	19490664	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Breast cancer	21364760	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Schizophrenia	19197363	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:1601 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:79882200-79895600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr13:79882200-79899200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr13:79882200-79907400	Weak transcription	Fetal Muscle Leg	muscle
4	chr13:79882200-79907600	Weak transcription	Brain Anterior Caudate	brain
5	chr13:79882200-79909800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr13:79882400-79904400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr13:79882400-79905000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr13:79882400-79911200	Weak transcription	Left Ventricle	heart
9	chr13:79882400-79911200	Weak transcription	Ovary	ovary
10	chr13:79882400-79914400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr13:79882400-79925000	Weak transcription	HSMMtube	muscle
12	chr13:79884000-79899400	Weak transcription	Psoas Muscle	Psoas
13	chr13:79884000-79905200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr13:79884400-79909000	Weak transcription	Brain Hippocampus Middle	brain
15	chr13:79884800-79895600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr13:79886400-79911200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr13:79886600-79900000	Weak transcription	Fetal Kidney	kidney
18	chr13:79886600-79950200	Weak transcription	Fetal Brain Male	brain
19	chr13:79887000-79904600	Weak transcription	Brain Substantia Nigra	brain
20	chr13:79887000-79907800	Weak transcription	Colon Smooth Muscle	Colon
21	chr13:79887200-79946600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr13:79887800-79907800	Weak transcription	NHLF	lung
23	chr13:79888000-79942800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr13:79888200-79947000	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr13:79888400-79900000	Weak transcription	A549	lung
26	chr13:79888400-79947000	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr13:79888600-79897400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr13:79889400-79896200	Weak transcription	Hela-S3	cervix
29	chr13:79889400-79905000	Weak transcription	Fetal Intestine Small	intestine
30	chr13:79889400-79909800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr13:79889600-79907800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr13:79889800-79899400	Weak transcription	K562	blood
33	chr13:79889800-79909800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr13:79889800-79916200	Weak transcription	Fetal Heart	heart
35	chr13:79890400-79905000	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr13:79890800-79895400	Weak transcription	Fetal Brain Female	brain
37	chr13:79890800-79896600	Strong transcription	HMEC	breast
38	chr13:79891000-79896600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr13:79891200-79895800	Strong transcription	GM12878-XiMat	blood
40	chr13:79891200-79896000	Strong transcription	Primary B cells from cord blood	blood
41	chr13:79891200-79897000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr13:79891200-79898000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr13:79891200-79900800	Strong transcription	HSMM	muscle
44	chr13:79891400-79911200	Weak transcription	Esophagus	oesophagus
45	chr13:79891600-79896200	Strong transcription	Placenta	Placenta
46	chr13:79891600-79896200	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr13:79891600-79897600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr13:79891600-79905000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr13:79891600-79911200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr13:79891600-79946800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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