Variant report

Variant	nsv1017025
Chromosome Location	chr5:75926278-75946265
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr5:75936794-75936839	GM12878	blood:	n/a	n/a
2	CBX3	chr5:75945721-75946038	K562	blood:	n/a	n/a
3	CEBPB	chr5:75928718-75928908	A549	lung:	n/a	chr5:75928880-75928893
4	CTCF	chr5:75937460-75937610	GM06990	blood:	n/a	chr5:75937530-75937546
5	CTCF	chr5:75937480-75937630	GM12871	blood:	n/a	chr5:75937530-75937546
6	CTCF	chr5:75937480-75937630	AG09309	skin:	n/a	chr5:75937530-75937546
7	CTCF	chr5:75937340-75937490	HAc	cerebellar:	n/a	n/a
8	CTCF	chr5:75937417-75937672	Pancreas_OC	pancreas:	n/a	chr5:75937530-75937546
9	CTCF	chr5:75937540-75937690	HAc	cerebellar:	n/a	n/a
10	CTCF	chr5:75937480-75937630	Caco-2	colon:	n/a	chr5:75937530-75937546
11	CTCF	chr5:75937400-75937550	K562	blood:	n/a	chr5:75937530-75937546
12	CTCF	chr5:75937420-75937570	HEK293	kidney:	n/a	chr5:75937530-75937546
13	CTCF	chr5:75937480-75937630	HVMF	connective:	n/a	chr5:75937530-75937546
14	CTCF	chr5:75937480-75937630	WI-38	lung:	n/a	chr5:75937530-75937546
15	CTCF	chr5:75937436-75937670	Kidney_OC	kidney:	n/a	chr5:75937530-75937546
16	CTCF	chr5:75938000-75938150	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr5:75937480-75937630	NHLF	lung:	n/a	chr5:75937530-75937546
18	CTCF	chr5:75937480-75937630	RPTEC	kidney:	n/a	chr5:75937530-75937546
19	CTCF	chr5:75937408-75937685	Gliobla	brain:	n/a	chr5:75937530-75937546
20	CTCF	chr5:75937420-75937570	SAEC	small airway:	n/a	chr5:75937530-75937546
21	CTCF	chr5:75937460-75937610	AG09319	gingival:	n/a	chr5:75937530-75937546
22	CTCF	chr5:75937460-75937610	GM12874	blood:	n/a	chr5:75937530-75937546
23	CTCF	chr5:75937440-75937590	GM06990	blood:	n/a	chr5:75937530-75937546
24	CTCF	chr5:75937481-75937575	GM19238	blood:	n/a	chr5:75937530-75937546
25	CTCF	chr5:75937460-75937610	AG04450	lung:	n/a	chr5:75937530-75937546
26	CTCF	chr5:75937419-75937656	GM10266	blood:	n/a	chr5:75937530-75937546
27	CTCF	chr5:75937440-75937590	GM12867	blood:	n/a	chr5:75937530-75937546
28	CTCF	chr5:75937387-75937688	HUVEC	blood vessel:	n/a	chr5:75937530-75937546
29	CTCF	chr5:75937460-75937610	AG10803	skin:	n/a	chr5:75937530-75937546
30	CTCF	chr5:75937440-75937590	AoAF	blood vessel:	n/a	chr5:75937530-75937546
31	CTCF	chr5:75937760-75937910	HVMF	connective:	n/a	n/a
32	CTCF	chr5:75937420-75937570	HL-60	blood:	n/a	chr5:75937530-75937546
33	CTCF	chr5:75937460-75937610	GM12868	blood:	n/a	chr5:75937530-75937546
34	CTCF	chr5:75936999-75937944	A549	lung:	n/a	chr5:75937530-75937546
35	CTCF	chr5:75937273-75937753	HCT-116	colon:	n/a	chr5:75937530-75937546
36	CTCF	chr5:75937467-75937614	Fibrobl	skin:	n/a	chr5:75937530-75937546
37	CTCF	chr5:75937440-75937590	GM12866	blood:	n/a	chr5:75937530-75937546
38	CTCF	chr5:75938160-75938310	GM12873	blood:	n/a	n/a
39	CTCF	chr5:75937400-75937699	H1-hESC	embryonic stem cell:	n/a	chr5:75937530-75937546
40	CTCF	chr5:75937460-75937610	HepG2	liver:	n/a	chr5:75937530-75937546
41	CTCF	chr5:75937322-75937743	A549	lung:	n/a	chr5:75937530-75937546
42	CTCF	chr5:75937480-75937630	GM12864	blood:	n/a	chr5:75937530-75937546
43	CTCF	chr5:75937303-75937912	IMR90	lung:	n/a	chr5:75937530-75937546
44	CTCF	chr5:75937480-75937630	GM12872	blood:	n/a	chr5:75937530-75937546
45	CTCF	chr5:75937460-75937610	BJ	skin:	n/a	chr5:75937530-75937546
46	CTCF	chr5:75936540-75936690	HFF	foreskin:	n/a	n/a
47	CTCF	chr5:75938000-75938150	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr5:75937420-75937570	HCM	heart:	n/a	chr5:75937530-75937546
49	CTCF	chr5:75937447-75937693	T-47D	breast:	n/a	chr5:75937530-75937546
50	CTCF	chr5:75937480-75937630	HEEpiC	esophagus:	n/a	chr5:75937530-75937546

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75938513-75938563	NHBE	bronchial:	n/a
2	chr5:75938513-75938563	ProgFib	skin:	n/a
3	chr5:75938513-75938563	LNCaP	prostate:	n/a
4	chr5:75938513-75938563	AG09319	gingival:	n/a
5	chr5:75938513-75938563	HRE	kidney:	n/a
6	chr5:75938513-75938563	GM12892	blood:	n/a
7	chr5:75938513-75938563	AoSMC	blood vessel:	n/a
8	chr5:75938513-75938563	BE2_C	brain:	n/a
9	chr5:75938513-75938563	ovcar-3	ovarian:	n/a
10	chr5:75938513-75938563	AG04449	skin:	fetal
11	chr5:75938513-75938563	CMK	blood:	n/a
12	chr5:75938513-75938563	BJ	skin:	n/a
13	chr5:75938513-75938563	HNPCEpiC	eye:	n/a
14	chr5:75938513-75938563	AG09309	skin:	n/a
15	chr5:75938513-75938563	HCM	heart:	n/a
16	chr5:75938513-75938563	NHDF-neo	bronchial:	n/a
17	chr5:75938513-75938563	SK-N-SH	brain:	n/a
18	chr5:75938513-75938563	NT2-D1	testis:	n/a
19	chr5:75938513-75938563	SAEC	small airway:	n/a
20	chr5:75938513-75938563	HL-60	blood:	n/a
21	chr5:75938513-75938563	PrEC	prostate:	n/a
22	chr5:75938513-75938563	U87	brain:	n/a
23	chr5:75938513-75938563	ECC-1	luminal epithelium:	n/a
24	chr5:75938513-75938563	GM06990	blood:	n/a
25	chr5:75938513-75938563	HIPEpiC	eye:	n/a
26	chr5:75938513-75938563	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:75938513-75938563	IMR90	lung:	fetal
28	chr5:75938513-75938563	GM12878	blood:	n/a
29	chr5:75938513-75938563	T-47D	breast:	n/a
30	chr5:75938513-75938563	HUVEC	blood vessel:	n/a
31	chr5:75938513-75938563	SK-N-MC	brain:	n/a
32	chr5:75938513-75938563	HCT-116	colon:	n/a
33	chr5:75938513-75938563	GM12891	blood:	n/a
34	chr5:75938513-75938563	SKMC	muscle:	n/a
35	chr5:75938513-75938563	HepG2	liver:	n/a
36	chr5:75938513-75938563	HEEpiC	esophagus:	n/a
37	chr5:75938513-75938563	Hepatocyte	liver:	n/a
38	chr5:75938513-75938563	NB4	blood:	n/a
39	chr5:75938513-75938563	HRPEpiC	eye:	n/a
40	chr5:75938513-75938563	PANC-1	pancreas:	n/a
41	chr5:75938513-75938563	PFSK-1	brain:	n/a
42	chr5:75938513-75938563	HRCEpiC	kidney:	n/a
43	chr5:75938513-75938563	GM19239	blood:	n/a
44	chr5:75938513-75938563	AG10803	skin:	n/a
45	chr5:75938513-75938563	Jurkat	blood:	n/a
46	chr5:75938513-75938563	H1-hESC	embryonic stem cell:	embryo
47	chr5:75938513-75938563	HCPEpiC	choroid plexus:	n/a
48	chr5:75938513-75938563	NH-A	brain:	n/a
49	chr5:75938513-75938563	MCF10A-Er-Src	breast:	n/a
50	chr5:75938513-75938563	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:75897975..75898494-chr5:75937296..75938025,2	MCF-7	breast:
2	chr5:75926553..75929296-chr5:75932910..75934652,2	K562	blood:
3	chr5:75927707..75929227-chr5:75935967..75938203,2	K562	blood:
4	chr5:75926553..75929296-chr5:75932910..75934652,2	K562	blood:
5	chr5:75921709..75924206-chr5:75928955..75931942,2	K562	blood:
6	chr5:75914946..75917081-chr5:75935923..75937441,2	K562	blood:
7	chr5:75927707..75929227-chr5:75935967..75938203,2	K562	blood:
8	chr5:75925160..75926957-chr5:75929982..75931882,2	MCF-7	breast:
9	chr5:75903037..75905690-chr5:75932365..75935110,2	K562	blood:
10	chr5:75896964..75897974-chr5:75936696..75938042,13	K562	blood:
11	chr5:75934487..75936821-chr5:75943605..75946585,2	MCF-7	breast:
12	chr5:75896478..75897915-chr5:75936605..75938172,9	MCF-7	breast:
13	chr5:75897247..75898569-chr5:75937033..75938017,10	MCF-7	breast:
14	chr5:75934487..75936821-chr5:75943605..75946585,2	MCF-7	breast:
15	chr5:75633387..75634022-chr5:75937052..75937701,2	K562	blood:
16	chr5:75897979..75898810-chr5:75937080..75938018,3	K562	blood:
17	chr5:75897714..75898323-chr5:75934762..75935296,2	MCF-7	breast:
18	chr5:75925160..75926957-chr5:75929982..75931882,2	MCF-7	breast:
19	chr5:75937138..75939935-chr5:76031767..76034422,2	K562	blood:

Variant related genes	Relation type
IQGAP2	TF binding region
IQGAP2	CpG island
ENSG00000145703	chromatin interactions
ENSG00000249713	chromatin interactions

Extended variants
information (count: 840 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs463272	chr5:75926278-75926279	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575238260	chr5:75926282-75926283	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368655738	chr5:75926283-75926284	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544338704	chr5:75926296-75926297	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552810072	chr5:75926321-75926322	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs3756523	chr5:75926357-75926358	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74598408	chr5:75926367-75926368	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368452097	chr5:75926375-75926376	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560788695	chr5:75926384-75926385	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs390086	chr5:75926401-75926402	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs373406532	chr5:75926426-75926427	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79363414	chr5:75926437-75926438	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192625186	chr5:75926499-75926500	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552407676	chr5:75926513-75926514	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562948877	chr5:75926515-75926516	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531662420	chr5:75926532-75926533	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200528509	chr5:75926541-75926542	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397840925	chr5:75926542-75926543	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201622648	chr5:75926543-75926544	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183439620	chr5:75926599-75926600	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538015534	chr5:75926619-75926620	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548047312	chr5:75926627-75926628	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115581340	chr5:75926640-75926641	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10715717	chr5:75926681-75926682	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112714456	chr5:75926684-75926685	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529864846	chr5:75926699-75926700	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566003846	chr5:75926773-75926774	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146782163	chr5:75926776-75926777	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs202000526	chr5:75926789-75926790	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs3797400	chr5:75926812-75926813	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs3797401	chr5:75926820-75926821	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs551880901	chr5:75926846-75926847	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568836311	chr5:75926847-75926848	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs457233	chr5:75926863-75926864	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs554662775	chr5:75926872-75926873	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs465959	chr5:75926873-75926874	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs139297156	chr5:75926879-75926880	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554440421	chr5:75926897-75926898	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143312633	chr5:75926970-75926971	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546481566	chr5:75926998-75926999	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370139105	chr5:75927003-75927004	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs406217	chr5:75927027-75927028	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs558823445	chr5:75927028-75927029	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs3797405	chr5:75927069-75927070	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs576399891	chr5:75927095-75927096	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576681797	chr5:75927097-75927098	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188331713	chr5:75927124-75927125	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561827689	chr5:75927137-75927138	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527817875	chr5:75927170-75927171	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs410262	chr5:75927188-75927189	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:86)

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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	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
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	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
Non-small cell lung cancer	21829676	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75879000-75934000	Weak transcription	Small Intestine	intestine
2	chr5:75880200-75933400	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr5:75882600-75969400	Weak transcription	Stomach Mucosa	stomach
4	chr5:75903800-75936200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:75903800-75943600	Weak transcription	Spleen	Spleen
6	chr5:75907800-75934600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr5:75908000-75928000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr5:75913400-75934600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr5:75914200-75953800	Weak transcription	Colonic Mucosa	Colon
10	chr5:75914400-75932800	Weak transcription	HepG2	liver
11	chr5:75918000-75943400	Weak transcription	Fetal Intestine Small	intestine
12	chr5:75918200-75943600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr5:75918400-75927200	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr5:75918400-75927800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr5:75919200-75943600	Weak transcription	Fetal Intestine Large	intestine
16	chr5:75919200-75955400	Weak transcription	Fetal Kidney	kidney
17	chr5:75919400-75928200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:75919400-75938200	Weak transcription	Pancreas	Pancrea
19	chr5:75919400-75944200	Weak transcription	Fetal Lung	lung
20	chr5:75921600-75938000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr5:75922000-75931000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr5:75922400-75928200	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr5:75922400-75929000	Strong transcription	Liver	Liver
24	chr5:75922600-75933400	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr5:75922800-75938000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr5:75923000-75933600	Weak transcription	GM12878-XiMat	blood
27	chr5:75923000-75938000	Weak transcription	Gastric	stomach
28	chr5:75923000-75938400	Weak transcription	Fetal Thymus	thymus
29	chr5:75923000-75944400	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr5:75923200-75928600	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr5:75923200-75933400	Strong transcription	Primary hematopoietic stem cells	blood
32	chr5:75923400-75928000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr5:75923400-75932400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr5:75923400-75934000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr5:75923400-75936200	Weak transcription	Fetal Stomach	stomach
36	chr5:75923600-75934400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:75923800-75933200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:75924000-75933400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr5:75924200-75927200	Weak transcription	Primary B cells from cord blood	blood
40	chr5:75924200-75929800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr5:75924200-75930000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr5:75924200-75943600	Weak transcription	Ovary	ovary
43	chr5:75924400-75930400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr5:75924400-75930600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr5:75924600-75930400	Weak transcription	K562	blood
46	chr5:75924800-75928200	Weak transcription	Placenta	Placenta
47	chr5:75924800-75936200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr5:75925200-75927600	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr5:75926000-75926600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:75926000-75926600	Enhancers	HUES48 Cell Line	embryonic stem cell

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