Variant report

Variant	nsv900931
Chromosome Location	chr13:95930685-95972496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1574)
CpG islands
(count:793)
Chromatin interactive
region (count:24)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1574 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95948833-95949093	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:95953613-95953696	K562	blood:	n/a	n/a
3	ARID3A	chr13:95937866-95938402	K562	blood:	n/a	n/a
4	ARID3A	chr13:95966752-95966960	K562	blood:	n/a	n/a
5	ARID3A	chr13:95949996-95950300	K562	blood:	n/a	n/a
6	ARID3A	chr13:95953876-95953898	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:95966627-95967073	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:95954220-95954222	K562	blood:	n/a	n/a
9	ARID3A	chr13:95952888-95953170	K562	blood:	n/a	n/a
10	ARID3A	chr13:95931642-95931648	K562	blood:	n/a	n/a
11	ARID3A	chr13:95969693-95970101	K562	blood:	n/a	n/a
12	ARID3A	chr13:95949726-95950320	HepG2	liver:	n/a	n/a
13	ATF1	chr13:95938012-95938442	K562	blood:	n/a	n/a
14	ATF2	chr13:95932871-95933559	GM12878	blood:	n/a	n/a
15	ATF2	chr13:95933714-95934499	GM12878	blood:	n/a	n/a
16	ATF2	chr13:95953752-95954132	GM12878	blood:	n/a	n/a
17	ATF2	chr13:95932888-95933441	GM12878	blood:	n/a	n/a
18	ATF3	chr13:95938112-95938426	K562	blood:	n/a	n/a
19	BACH1	chr13:95969790-95969856	K562	blood:	n/a	n/a
20	BACH1	chr13:95948824-95949086	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr13:95953247-95954203	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr13:95933185-95933517	GM12878	blood:	n/a	chr13:95933299-95933308
23	BCL3	chr13:95949792-95950231	A549	lung:	n/a	n/a
24	BCLAF1	chr13:95953476-95954069	GM12878	blood:	n/a	chr13:95953785-95953794 chr13:95953720-95953733 chr13:95953620-95953633
25	BCLAF1	chr13:95952941-95953394	GM12878	blood:	n/a	n/a
26	BCLAF1	chr13:95951836-95952208	GM12878	blood:	n/a	chr13:95952082-95952091
27	BCLAF1	chr13:95933136-95933564	GM12878	blood:	n/a	chr13:95933299-95933308
28	BCLAF1	chr13:95937861-95938393	K562	blood:	n/a	n/a
29	BHLHE40	chr13:95966774-95966999	K562	blood:	n/a	n/a
30	BHLHE40	chr13:95951572-95951726	K562	blood:	n/a	n/a
31	BHLHE40	chr13:95931372-95931664	K562	blood:	n/a	n/a
32	BHLHE40	chr13:95951472-95951807	GM12878	blood:	n/a	n/a
33	BHLHE40	chr13:95937918-95938449	K562	blood:	n/a	n/a
34	BHLHE40	chr13:95969437-95969892	K562	blood:	n/a	n/a
35	BHLHE40	chr13:95953007-95954599	K562	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
36	BHLHE40	chr13:95934235-95934425	GM12878	blood:	n/a	n/a
37	BHLHE40	chr13:95953400-95954315	HepG2	liver:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
38	BHLHE40	chr13:95953022-95954602	GM12878	blood:	n/a	chr13:95953784-95953800 chr13:95953446-95953462 chr13:95953443-95953459
39	BHLHE40	chr13:95954115-95954309	A549	lung:	n/a	n/a
40	BRCA1	chr13:95966541-95967031	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr13:95951787-95951795	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr13:95952976-95953062	GM12878	blood:	n/a	n/a
43	BRCA1	chr13:95972005-95972368	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr13:95953989-95954014	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr13:95948905-95949128	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr13:95953565-95953620	HepG2	liver:	n/a	n/a
47	BRCA1	chr13:95955316-95955425	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr13:95938077-95938390	K562	blood:	n/a	n/a
49	CBX3	chr13:95937978-95938484	K562	blood:	n/a	n/a
50	CBX3	chr13:95953672-95954674	K562	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95953574-95953624	ECC-1	luminal epithelium:	n/a
2	chr13:95954080-95954130	MCF10A-Er-Src	breast:	n/a
3	chr13:95954382-95954432	GM12878	blood:	n/a
4	chr13:95954382-95954432	HAEpiC	amniotic membrane:	n/a
5	chr13:95953505-95953555	SAEC	small airway:	n/a
6	chr13:95953482-95953532	HRCEpiC	kidney:	n/a
7	chr13:95952937-95952987	H1-hESC	embryonic stem cell:	embryo
8	chr13:95958190-95958240	MCF-7	breast:	n/a
9	chr13:95954080-95954130	GM12878	blood:	n/a
10	chr13:95953574-95953624	HCM	heart:	n/a
11	chr13:95954534-95954584	HEEpiC	esophagus:	n/a
12	chr13:95954382-95954432	BJ	skin:	n/a
13	chr13:95952902-95952952	U87	brain:	n/a
14	chr13:95954382-95954432	IMR90	lung:	fetal
15	chr13:95953229-95953279	HRPEpiC	eye:	n/a
16	chr13:95958190-95958240	Caco-2	colon:	n/a
17	chr13:95953941-95953991	HMEC	breast:	n/a
18	chr13:95952937-95952987	PFSK-1	brain:	n/a
19	chr13:95953505-95953555	LNCaP	prostate:	n/a
20	chr13:95958190-95958240	PANC-1	pancreas:	n/a
21	chr13:95954534-95954584	HCF	heart:	n/a
22	chr13:95958190-95958240	HCPEpiC	choroid plexus:	n/a
23	chr13:95954534-95954584	GM19239	blood:	n/a
24	chr13:95933097-95933147	LNCaP	prostate:	n/a
25	chr13:95953482-95953532	HRPEpiC	eye:	n/a
26	chr13:95954534-95954584	BJ	skin:	n/a
27	chr13:95953505-95953555	NB4	blood:	n/a
28	chr13:95932467-95932517	SK-N-SH_RA	brain:	n/a
29	chr13:95954080-95954130	SK-N-MC	brain:	n/a
30	chr13:95953229-95953279	AG04450	lung:	fetal
31	chr13:95954080-95954130	HRPEpiC	eye:	n/a
32	chr13:95958190-95958240	K562	blood:	n/a
33	chr13:95953229-95953279	PrEC	prostate:	n/a
34	chr13:95953574-95953624	SK-N-SH	brain:	n/a
35	chr13:95932467-95932517	HCT-116	colon:	n/a
36	chr13:95953505-95953555	A549	lung:	n/a
37	chr13:95932467-95932517	AoSMC	blood vessel:	n/a
38	chr13:95953482-95953532	NHDF-neo	bronchial:	n/a
39	chr13:95952902-95952952	BE2_C	brain:	n/a
40	chr13:95954080-95954130	IMR90	lung:	fetal
41	chr13:95932467-95932517	HepG2	liver:	n/a
42	chr13:95953941-95953991	HNPCEpiC	eye:	n/a
43	chr13:95933097-95933147	NT2-D1	testis:	n/a
44	chr13:95954080-95954130	CMK	blood:	n/a
45	chr13:95954382-95954432	GM19239	blood:	n/a
46	chr13:95953574-95953624	HIPEpiC	eye:	n/a
47	chr13:95933097-95933147	PrEC	prostate:	n/a
48	chr13:95953574-95953624	AG10803	skin:	n/a
49	chr13:95952902-95952952	T-47D	breast:	n/a
50	chr13:95952937-95952987	LNCaP	prostate:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:95927378..95929483-chr13:95944855..95946497,2	K562	blood:
2	chr13:95929149..95932336-chr13:95935085..95938343,4	K562	blood:
3	chr13:95952688..95955357-chr13:95971303..95973623,2	K562	blood:
4	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
5	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
6	chr13:95935600..95938321-chr13:95941530..95943293,2	K562	blood:
7	chr13:95953151..95954875-chr13:95967251..95970117,3	K562	blood:
8	chr13:95941801..95944628-chr13:95951668..95954377,2	MCF-7	breast:
9	chr13:95844110..95844687-chr13:95948689..95949204,2	MCF-7	breast:
10	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:
11	chr13:95845563..95847405-chr13:95944839..95947304,2	K562	blood:
12	chr13:95946953..95949885-chr13:95950441..95955332,5	K562	blood:
13	chr13:95946953..95949885-chr13:95950238..95955332,4	K562	blood:
14	chr13:95953151..95954875-chr13:95967251..95969604,2	K562	blood:
15	chr13:95948894..95949810-chr13:96056285..96057228,3	MCF-7	breast:
16	chr13:95929149..95932336-chr13:95935085..95938343,4	K562	blood:
17	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
18	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:
19	chr13:95922109..95924473-chr13:95936856..95939759,2	K562	blood:
20	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
21	chr1:149223926..149224513-chr13:95953070..95953746,2	Hela-S3	cervix:
22	chr13:60970248..60971090-chr13:95952535..95953452,2	Hela-S3	cervix:
23	chr13:95950632..95952981-chr13:95955199..95956850,2	K562	blood:
24	chr13:95931327..95933216-chr13:95948298..95949937,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCC4-1	chr13:95954705-95955669	XLOC_010696
2	lnc-CLDN10-6	chr13:95957471-95958654	NONHSAT034755
3	lnc-ABCC4-1	chr13:95956351-95956401	XLOC_010696

No data

Variant related genes	Relation type
ABCC4	TF binding region
RNY3P8	TF binding region
ABCC4	CpG island
RNY3P8	CpG island
ENSG00000083544	chromatin interactions
ENSG00000125257	chromatin interactions
ENSG00000206737	chromatin interactions
SMAD4	miRNA target sites

Extended variants
information (count: 1725 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1725 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10508017	chr13:95930685-95930686	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371132396	chr13:95930694-95930695	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374550431	chr13:95930696-95930697	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs55939936	chr13:95930711-95930712	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs55884275	chr13:95930714-95930715	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543746048	chr13:95930729-95930730	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563439589	chr13:95930740-95930741	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs367544622	chr13:95930776-95930777	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537259584	chr13:95930777-95930778	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552082727	chr13:95930780-95930781	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529146296	chr13:95930786-95930787	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571934672	chr13:95930787-95930788	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs56157443	chr13:95930882-95930883	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs367871948	chr13:95930976-95930977	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531252053	chr13:95931004-95931005	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574052362	chr13:95931061-95931062	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs71113905	chr13:95931086-95931087	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562035655	chr13:95931099-95931100	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181218215	chr13:95931102-95931103	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79407217	chr13:95931174-95931175	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9524878	chr13:95931182-95931183	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547899102	chr13:95931187-95931188	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571069327	chr13:95931193-95931194	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145218836	chr13:95931195-95931196	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4148425	chr13:95931231-95931232	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs367679607	chr13:95931242-95931243	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550947708	chr13:95931262-95931263	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567659375	chr13:95931341-95931342	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570267059	chr13:95931372-95931373	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149135579	chr13:95931466-95931467	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186267741	chr13:95931489-95931490	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4148424	chr13:95931490-95931491	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs4148423	chr13:95931595-95931596	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs118046467	chr13:95931602-95931603	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs534539325	chr13:95931627-95931628	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs577620925	chr13:95931694-95931695	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs190639950	chr13:95931708-95931709	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs114529612	chr13:95931758-95931759	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs573732146	chr13:95931766-95931767	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs542863857	chr13:95931859-95931860	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577490012	chr13:95931865-95931866	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145166997	chr13:95931903-95931904	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527793119	chr13:95931942-95931943	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4148422	chr13:95931992-95931993	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs564316735	chr13:95931994-95931995	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9524879	chr13:95932010-95932011	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs9524880	chr13:95932017-95932018	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146538737	chr13:95932029-95932030	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79828993	chr13:95932055-95932056	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529414712	chr13:95932071-95932072	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	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
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1011 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95913600-95932800	Weak transcription	Primary B cells from peripheral blood	blood
2	chr13:95917000-95931400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr13:95920200-95952800	Weak transcription	Aorta	Aorta
4	chr13:95923800-95941200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr13:95924200-95930800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr13:95924200-95932800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr13:95924600-95952600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr13:95924800-95932200	Weak transcription	HUVEC	blood vessel
9	chr13:95925800-95932200	Weak transcription	Psoas Muscle	Psoas
10	chr13:95926600-95952400	Weak transcription	Brain Hippocampus Middle	brain
11	chr13:95926800-95931400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr13:95926800-95932800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr13:95926800-95948600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr13:95927000-95931400	Enhancers	K562	blood
15	chr13:95927000-95932000	Weak transcription	Right Ventricle	heart
16	chr13:95927000-95932800	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr13:95927000-95937800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr13:95927000-95938000	Weak transcription	Colonic Mucosa	Colon
19	chr13:95927200-95932000	Weak transcription	Lung	lung
20	chr13:95927200-95941600	Weak transcription	Gastric	stomach
21	chr13:95927800-95932000	Weak transcription	Brain Anterior Caudate	brain
22	chr13:95928000-95931000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr13:95928400-95931200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr13:95928400-95931800	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr13:95928400-95932000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr13:95928400-95932600	Weak transcription	HSMMtube	muscle
27	chr13:95928400-95932600	Weak transcription	NH-A	brain
28	chr13:95928400-95933800	Weak transcription	Fetal Kidney	kidney
29	chr13:95928400-95934000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr13:95928400-95937600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr13:95928400-95937800	Weak transcription	Fetal Intestine Small	intestine
32	chr13:95928600-95931800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr13:95928600-95932000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr13:95928600-95932200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr13:95928600-95932200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr13:95928600-95932200	Weak transcription	HSMM	muscle
37	chr13:95928600-95932800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr13:95928600-95932800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr13:95928600-95932800	Weak transcription	Osteobl	bone
40	chr13:95928600-95933000	Weak transcription	Rectal Smooth Muscle	rectum
41	chr13:95928600-95933200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr13:95928800-95932200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr13:95928800-95932600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr13:95928800-95932800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr13:95928800-95932800	Weak transcription	Fetal Stomach	stomach
46	chr13:95928800-95932800	Weak transcription	NHEK	skin
47	chr13:95929000-95931400	Weak transcription	NHLF	lung
48	chr13:95929000-95932200	Weak transcription	Colon Smooth Muscle	Colon
49	chr13:95929000-95932800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr13:95929000-95932800	Weak transcription	Fetal Lung	lung

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