Variant report

Variant	nsv881736
Chromosome Location	chr5:61833440-61877628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:296)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:61834143-61834798	K562	blood:	n/a	n/a
2	ATF1	chr5:61834328-61834785	K562	blood:	n/a	n/a
3	ATF2	chr5:61870304-61870858	GM12878	blood:	n/a	n/a
4	BACH1	chr5:61834564-61834771	K562	blood:	n/a	n/a
5	BACH1	chr5:61865990-61866018	K562	blood:	n/a	n/a
6	BACH1	chr5:61847461-61847507	K562	blood:	n/a	n/a
7	BATF	chr5:61865376-61865608	GM12878	blood:	n/a	chr5:61865577-61865585
8	BATF	chr5:61870477-61870741	GM12878	blood:	n/a	n/a
9	BATF	chr5:61870405-61870771	GM12878	blood:	n/a	n/a
10	BCLAF1	chr5:61870371-61870825	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:61834289-61834768	K562	blood:	n/a	n/a
12	BHLHE40	chr5:61872555-61872604	K562	blood:	n/a	n/a
13	BRCA1	chr5:61834474-61834740	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr5:61863983-61864320	K562	blood:	n/a	n/a
15	CBX3	chr5:61834280-61834852	K562	blood:	n/a	n/a
16	CBX3	chr5:61863976-61864361	K562	blood:	n/a	n/a
17	CCNT2	chr5:61834507-61834787	K562	blood:	n/a	n/a
18	CCNT2	chr5:61876573-61876767	K562	blood:	n/a	n/a
19	CEBPB	chr5:61861251-61861340	A549	lung:	n/a	chr5:61861263-61861274
20	CEBPB	chr5:61851779-61852116	K562	blood:	n/a	chr5:61851945-61851956
21	CEBPB	chr5:61834346-61834856	A549	lung:	n/a	n/a
22	CEBPB	chr5:61851773-61852131	Hela-S3	cervix:	n/a	chr5:61851945-61851956
23	CEBPB	chr5:61834383-61834832	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:61851767-61852130	HepG2	liver:	n/a	chr5:61851945-61851956
25	CEBPB	chr5:61851780-61852127	IMR90	lung:	n/a	chr5:61851945-61851956
26	CEBPB	chr5:61851781-61852057	H1-hESC	embryonic stem cell:	n/a	chr5:61851945-61851956
27	CEBPB	chr5:61851811-61852123	A549	lung:	n/a	chr5:61851945-61851956
28	CEBPB	chr5:61834390-61834854	IMR90	lung:	n/a	n/a
29	CEBPB	chr5:61834454-61834768	K562	blood:	n/a	n/a
30	CEBPB	chr5:61861241-61861438	HepG2	liver:	n/a	chr5:61861263-61861274
31	CEBPB	chr5:61845040-61845363	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:61845071-61845358	A549	lung:	n/a	n/a
33	CEBPB	chr5:61834005-61834821	K562	blood:	n/a	n/a
34	CEBPB	chr5:61838622-61838854	A549	lung:	n/a	chr5:61838755-61838764 chr5:61838673-61838686 chr5:61838754-61838765 chr5:61838753-61838764 chr5:61838673-61838686
35	CEBPB	chr5:61834394-61834792	A549	lung:	n/a	n/a
36	CEBPB	chr5:61834495-61834802	MCF-7	breast:	n/a	n/a
37	CEBPB	chr5:61834195-61834842	K562	blood:	n/a	n/a
38	CEBPB	chr5:61838580-61838893	HepG2	liver:	n/a	chr5:61838755-61838764 chr5:61838673-61838686 chr5:61838754-61838765 chr5:61838753-61838764 chr5:61838673-61838686
39	CEBPB	chr5:61834427-61834676	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:61845040-61845323	HepG2	liver:	n/a	n/a
41	CEBPD	chr5:61834354-61834839	K562	blood:	n/a	n/a
42	CEBPD	chr5:61834377-61834847	K562	blood:	n/a	n/a
43	CREB1	chr5:61834136-61835006	K562	blood:	n/a	n/a
44	CREB1	chr5:61834317-61834929	K562	blood:	n/a	n/a
45	CTCF	chr5:61858860-61859010	MCF-7	breast:	n/a	chr5:61858899-61858908
46	CTCF	chr5:61858820-61858970	HPF	lung:	n/a	chr5:61858899-61858908
47	CTCF	chr5:61864945-61865031	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr5:61858840-61858990	HEK293	kidney:	n/a	chr5:61858899-61858908
49	CTCF	chr5:61858840-61858990	GM12873	blood:	n/a	chr5:61858899-61858908
50	CTCF	chr5:61858877-61858910	LNCaP	prostate:	n/a	chr5:61858899-61858908

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61844855-61844905	SAEC	small airway:	n/a
2	chr5:61844855-61844905	HMEC	breast:	n/a
3	chr5:61876634-61876684	K562	blood:	n/a
4	chr5:61844855-61844905	AoSMC	blood vessel:	n/a
5	chr5:61874017-61874067	GM19239	blood:	n/a
6	chr5:61876634-61876684	SAEC	small airway:	n/a
7	chr5:61876634-61876684	LNCaP	prostate:	n/a
8	chr5:61876634-61876684	AoSMC	blood vessel:	n/a
9	chr5:61874017-61874067	HMEC	breast:	n/a
10	chr5:61874017-61874067	HEEpiC	esophagus:	n/a
11	chr5:61874017-61874067	T-47D	breast:	n/a
12	chr5:61876634-61876684	ovcar-3	ovarian:	n/a
13	chr5:61874017-61874067	HL-60	blood:	n/a
14	chr5:61844855-61844905	HNPCEpiC	eye:	n/a
15	chr5:61874017-61874067	HRE	kidney:	n/a
16	chr5:61844855-61844905	PFSK-1	brain:	n/a
17	chr5:61874017-61874067	GM12891	blood:	n/a
18	chr5:61844855-61844905	HEEpiC	esophagus:	n/a
19	chr5:61876634-61876684	BE2_C	brain:	n/a
20	chr5:61874017-61874067	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:61876634-61876684	HCF	heart:	n/a
22	chr5:61844855-61844905	BE2_C	brain:	n/a
23	chr5:61844855-61844905	BJ	skin:	n/a
24	chr5:61844855-61844905	HRCEpiC	kidney:	n/a
25	chr5:61874017-61874067	ECC-1	luminal epithelium:	n/a
26	chr5:61844855-61844905	PrEC	prostate:	n/a
27	chr5:61876634-61876684	HUVEC	blood vessel:	n/a
28	chr5:61876634-61876684	HMEC	breast:	n/a
29	chr5:61876634-61876684	SKMC	muscle:	n/a
30	chr5:61874017-61874067	HCM	heart:	n/a
31	chr5:61874017-61874067	Caco-2	colon:	n/a
32	chr5:61876634-61876684	HCM	heart:	n/a
33	chr5:61876634-61876684	NHDF-neo	bronchial:	n/a
34	chr5:61876634-61876684	NH-A	brain:	n/a
35	chr5:61844855-61844905	Hepatocyte	liver:	n/a
36	chr5:61876634-61876684	PrEC	prostate:	n/a
37	chr5:61844855-61844905	ECC-1	luminal epithelium:	n/a
38	chr5:61844855-61844905	ProgFib	skin:	n/a
39	chr5:61844855-61844905	HAEpiC	amniotic membrane:	n/a
40	chr5:61874017-61874067	AoSMC	blood vessel:	n/a
41	chr5:61874017-61874067	HAEpiC	amniotic membrane:	n/a
42	chr5:61874017-61874067	HNPCEpiC	eye:	n/a
43	chr5:61844855-61844905	MCF-7	breast:	n/a
44	chr5:61874017-61874067	AG09319	gingival:	n/a
45	chr5:61844855-61844905	HCF	heart:	n/a
46	chr5:61844855-61844905	GM19239	blood:	n/a
47	chr5:61876634-61876684	HRE	kidney:	n/a
48	chr5:61876634-61876684	Jurkat	blood:	n/a
49	chr5:61874017-61874067	SKMC	muscle:	n/a
50	chr5:61874017-61874067	LNCaP	prostate:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:61833675..61836577-chr5:61862911..61865153,3	K562	blood:
2	chr5:61833268..61834812-chr5:61850872..61852954,2	K562	blood:
3	chr5:61826046..61828158-chr5:61830735..61833492,2	K562	blood:
4	chr5:61829519..61831113-chr5:61834353..61836301,2	MCF-7	breast:
5	chr5:61865017..61866532-chr5:61879181..61880802,2	K562	blood:
6	chr5:61833161..61835046-chr5:61842892..61845396,3	K562	blood:
7	chr5:61875725..61878816-chr5:61880010..61882591,3	MCF-7	breast:
8	chr5:61833675..61836577-chr5:61862911..61865153,3	K562	blood:
9	chr5:61875507..61877206-chr5:61878546..61880725,2	K562	blood:
10	chr5:61833161..61835046-chr5:61842892..61845396,3	K562	blood:
11	chr5:61833268..61834812-chr5:61850872..61852954,2	K562	blood:
12	chr5:61820977..61823095-chr5:61832322..61835003,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIMT1-2	chr5:61871778-61872098	NONHSAT101715
2	lnc-DIMT1-1	chr5:61857686-61858043	NONHSAT101714
3	lnc-LRRC70-1	chr5:61876281-61877269	NONHSAT101716
4	lnc-LRRC70-1	chr5:61856523-61856832	NONHSAT101713
5	lnc-LRRC70-1	chr5:61856963-61857084	NONHSAT101713
6	lnc-LRRC70-1	chr5:61874664-61874762	NONHSAT101716
7	lnc-LRRC70-1	chr5:61875228-61875310	NONHSAT101716

No data

Variant related genes	Relation type
ENSG00000241991	TF binding region
LRRC70	TF binding region
IPO11	TF binding region
ENSG00000240436	TF binding region
ENSG00000241991	CpG island
LRRC70	CpG island
IPO11	CpG island
ENSG00000240436	CpG island

Extended variants
information (count: 1702 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1702 , 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	rs7737525	chr5:61833440-61833441	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371520647	chr5:61833467-61833468	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191633672	chr5:61833482-61833483	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555609294	chr5:61833483-61833484	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182949471	chr5:61833485-61833486	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187494027	chr5:61833512-61833513	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542824432	chr5:61833602-61833603	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193289750	chr5:61833644-61833645	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566171610	chr5:61833674-61833675	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114581688	chr5:61833676-61833677	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578060411	chr5:61833720-61833721	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115100905	chr5:61833771-61833772	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185474225	chr5:61833789-61833790	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528346200	chr5:61833835-61833836	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542021391	chr5:61833846-61833847	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563067865	chr5:61833871-61833872	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561686526	chr5:61833935-61833936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530566355	chr5:61833949-61833950	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550252094	chr5:61833956-61833957	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570148665	chr5:61833973-61833974	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375657153	chr5:61833980-61833981	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140465785	chr5:61833984-61833985	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189125405	chr5:61834005-61834006	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs192058103	chr5:61834015-61834016	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs367756801	chr5:61834024-61834025	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs533530918	chr5:61834038-61834039	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs558453399	chr5:61834054-61834055	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs577032717	chr5:61834061-61834062	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs370583541	chr5:61834109-61834110	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs535736392	chr5:61834145-61834146	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs555929564	chr5:61834150-61834151	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs569468246	chr5:61834159-61834160	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs149982147	chr5:61834166-61834167	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs558264580	chr5:61834222-61834223	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs578090990	chr5:61834230-61834231	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540653107	chr5:61834248-61834249	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561448974	chr5:61834294-61834295	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371997232	chr5:61834308-61834309	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184201798	chr5:61834315-61834316	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145626028	chr5:61834319-61834320	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188629984	chr5:61834343-61834344	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537652700	chr5:61834351-61834352	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561960779	chr5:61834356-61834357	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148892160	chr5:61834377-61834378	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543933867	chr5:61834390-61834391	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563862579	chr5:61834395-61834396	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537596715	chr5:61834422-61834423	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556277881	chr5:61834457-61834458	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12109582	chr5:61834469-61834470	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546586025	chr5:61834475-61834476	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61728800-61838200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr5:61730000-61834200	Weak transcription	Gastric	stomach
3	chr5:61739200-61862800	Weak transcription	Brain Substantia Nigra	brain
4	chr5:61744800-61838600	Weak transcription	Colonic Mucosa	Colon
5	chr5:61748000-61862800	Weak transcription	Right Ventricle	heart
6	chr5:61758800-61890000	Weak transcription	Small Intestine	intestine
7	chr5:61759000-61834200	Weak transcription	Esophagus	oesophagus
8	chr5:61760800-61847200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:61764000-61833800	Weak transcription	Fetal Brain Female	brain
10	chr5:61764000-61858200	Weak transcription	Placenta	Placenta
11	chr5:61764200-61895800	Weak transcription	Pancreas	Pancrea
12	chr5:61766200-61849800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr5:61771200-61864800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:61771400-61863000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:61772200-61850800	Weak transcription	HSMMtube	muscle
16	chr5:61772600-61842000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:61781600-61867600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr5:61787200-61836000	Weak transcription	Colon Smooth Muscle	Colon
19	chr5:61787400-61866800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr5:61789400-61835400	Weak transcription	Fetal Brain Male	brain
21	chr5:61793600-61905000	Weak transcription	NHEK	skin
22	chr5:61795000-61834000	Weak transcription	Ovary	ovary
23	chr5:61795200-61850600	Weak transcription	Fetal Intestine Small	intestine
24	chr5:61796600-61866600	Weak transcription	Osteobl	bone
25	chr5:61796800-61899000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr5:61797000-61833800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr5:61797000-61861200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr5:61802600-61889000	Weak transcription	NH-A	brain
29	chr5:61803000-61904400	Weak transcription	Fetal Kidney	kidney
30	chr5:61803200-61836200	Weak transcription	Fetal Intestine Large	intestine
31	chr5:61803200-61875000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr5:61803400-61855000	Weak transcription	HSMM	muscle
33	chr5:61803400-61863600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr5:61804400-61865200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr5:61806800-61863400	Weak transcription	Lung	lung
36	chr5:61812000-61834400	Weak transcription	Fetal Muscle Trunk	muscle
37	chr5:61812000-61834600	Weak transcription	HMEC	breast
38	chr5:61812200-61865200	Weak transcription	HUVEC	blood vessel
39	chr5:61814400-61834200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr5:61815000-61861400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:61815200-61890600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr5:61816000-61857800	Weak transcription	Fetal Stomach	stomach
43	chr5:61816200-61862200	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr5:61819200-61834600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:61819200-61860400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:61819400-61838000	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr5:61819800-61838000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr5:61819800-61861600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:61821200-61836200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr5:61821400-61838600	Weak transcription	Spleen	Spleen

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