Variant report

Variant	esv1795990
Chromosome Location	chr5:80043404-80066135
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:80051483-80051764	K562	blood:	n/a	n/a
2	ATF2	chr5:80051440-80051947	GM12878	blood:	n/a	n/a
3	ATF2	chr5:80051504-80051911	GM12878	blood:	n/a	n/a
4	BATF	chr5:80056062-80056380	GM12878	blood:	n/a	chr5:80056222-80056232 chr5:80056221-80056232
5	BATF	chr5:80051503-80051795	GM12878	blood:	n/a	chr5:80051646-80051655
6	BCL11A	chr5:80051567-80051822	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:80050740-80051012	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:80051501-80051916	GM12878	blood:	n/a	n/a
9	BCLAF1	chr5:80051395-80051963	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:80050718-80051149	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:80051470-80051933	GM12878	blood:	n/a	chr5:80051624-80051645
12	BRCA1	chr5:80051524-80051588	GM12878	blood:	n/a	n/a
13	CEBPB	chr5:80059080-80059398	K562	blood:	n/a	chr5:80059211-80059222
14	CEBPB	chr5:80059044-80059381	IMR90	lung:	n/a	chr5:80059211-80059222
15	CEBPB	chr5:80059092-80059390	A549	lung:	n/a	chr5:80059211-80059222
16	CEBPB	chr5:80060041-80060199	A549	lung:	n/a	n/a
17	CEBPB	chr5:80059049-80059395	HepG2	liver:	n/a	chr5:80059211-80059222
18	CEBPB	chr5:80059045-80059408	Hela-S3	cervix:	n/a	chr5:80059211-80059222
19	CHD1	chr5:80051187-80051849	GM12878	blood:	n/a	n/a
20	CHD2	chr5:80051413-80051875	GM12878	blood:	n/a	n/a
21	CHD2	chr5:80056561-80056703	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr5:80050742-80051072	GM12878	blood:	n/a	n/a
23	CREB1	chr5:80051293-80052015	GM12878	blood:	n/a	n/a
24	CTCF	chr5:80051722-80051756	GM12878	blood:	n/a	n/a
25	CTCF	chr5:80057120-80057165	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr5:80052620-80052770	GM12869	blood:	n/a	n/a
27	CTCF	chr5:80051040-80051190	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr5:80052100-80052250	GM12872	blood:	n/a	n/a
29	CUX1	chr5:80049295-80049308	GM12878	blood:	n/a	n/a
30	CUX1	chr5:80052469-80052488	GM12878	blood:	n/a	n/a
31	CUX1	chr5:80051471-80051868	GM12878	blood:	n/a	n/a
32	EBF1	chr5:80051528-80051867	GM12878	blood:	n/a	n/a
33	EBF1	chr5:80050699-80051065	GM12878	blood:	n/a	chr5:80050871-80050882
34	EBF1	chr5:80050636-80051077	GM12878	blood:	n/a	chr5:80050871-80050882
35	EBF1	chr5:80050672-80051087	GM12878	blood:	n/a	chr5:80050871-80050882
36	ELF1	chr5:80057045-80057278	K562	blood:	n/a	n/a
37	ELK1	chr5:80050869-80050994	GM12878	blood:	n/a	n/a
38	EP300	chr5:80051460-80051917	GM12878	blood:	n/a	n/a
39	EP300	chr5:80051453-80051902	GM12878	blood:	n/a	n/a
40	EP300	chr5:80050681-80051192	GM12878	blood:	n/a	n/a
41	EP300	chr5:80050691-80051101	GM12878	blood:	n/a	n/a
42	EP300	chr5:80051525-80051844	GM12878	blood:	n/a	n/a
43	EP300	chr5:80050738-80051003	GM12878	blood:	n/a	n/a
44	FOS	chr5:80059040-80059361	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr5:80059057-80059304	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr5:80043317-80043617	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr5:80057860-80058161	HUVEC	blood vessel:	n/a	chr5:80058008-80058016 chr5:80058008-80058017 chr5:80057993-80058000 chr5:80058006-80058017 chr5:80057988-80057999 chr5:80058009-80058016 chr5:80057992-80058000 chr5:80058007-80058017
48	FOS	chr5:80058984-80059396	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr5:80043317-80043598	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr5:80057799-80058185	MCF10A-Er-Src	breast:	n/a	chr5:80058008-80058016 chr5:80058008-80058017 chr5:80057993-80058000 chr5:80058006-80058017 chr5:80057988-80057999 chr5:80058009-80058016 chr5:80057992-80058000 chr5:80058007-80058017

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:80050837-80050887	H1-hESC	embryonic stem cell:	embryo
2	chr5:80060102-80060152	HepG2	liver:	n/a
3	chr5:80050837-80050887	MCF10A-Er-Src	breast:	n/a
4	chr5:80060102-80060152	GM12878	blood:	n/a
5	chr5:80050837-80050887	ProgFib	skin:	n/a
6	chr5:80060102-80060152	Hela-S3	cervix:	n/a
7	chr5:80050837-80050887	NH-A	brain:	n/a
8	chr5:80060102-80060152	HCT-116	colon:	n/a
9	chr5:80050837-80050887	MCF-7	breast:	n/a
10	chr5:80060102-80060152	NHBE	bronchial:	n/a
11	chr5:80060102-80060152	ECC-1	luminal epithelium:	n/a
12	chr5:80060102-80060152	U87	brain:	n/a
13	chr5:80050837-80050887	HCM	heart:	n/a
14	chr5:80050837-80050887	BE2_C	brain:	n/a
15	chr5:80060102-80060152	PANC-1	pancreas:	n/a
16	chr5:80050837-80050887	GM19239	blood:	n/a
17	chr5:80050837-80050887	Hepatocyte	liver:	n/a
18	chr5:80060102-80060152	H1-hESC	embryonic stem cell:	embryo
19	chr5:80060102-80060152	ProgFib	skin:	n/a
20	chr5:80050837-80050887	Jurkat	blood:	n/a
21	chr5:80050837-80050887	HepG2	liver:	n/a
22	chr5:80050837-80050887	HEEpiC	esophagus:	n/a
23	chr5:80050837-80050887	AG04450	lung:	fetal
24	chr5:80060102-80060152	HRE	kidney:	n/a
25	chr5:80060102-80060152	HRPEpiC	eye:	n/a
26	chr5:80050837-80050887	SKMC	muscle:	n/a
27	chr5:80060102-80060152	A549	lung:	n/a
28	chr5:80060102-80060152	Hepatocyte	liver:	n/a
29	chr5:80050837-80050887	U87	brain:	n/a
30	chr5:80050837-80050887	AG09309	skin:	n/a
31	chr5:80060102-80060152	GM06990	blood:	n/a
32	chr5:80050837-80050887	AoSMC	blood vessel:	n/a
33	chr5:80060102-80060152	HCF	heart:	n/a
34	chr5:80060102-80060152	SAEC	small airway:	n/a
35	chr5:80050837-80050887	HUVEC	blood vessel:	n/a
36	chr5:80050837-80050887	Hela-S3	cervix:	n/a
37	chr5:80050837-80050887	ECC-1	luminal epithelium:	n/a
38	chr5:80050837-80050887	GM12892	blood:	n/a
39	chr5:80050837-80050887	HCPEpiC	choroid plexus:	n/a
40	chr5:80050837-80050887	GM06990	blood:	n/a
41	chr5:80060102-80060152	HMEC	breast:	n/a
42	chr5:80060102-80060152	NB4	blood:	n/a
43	chr5:80060102-80060152	AG10803	skin:	n/a
44	chr5:80060102-80060152	HUVEC	blood vessel:	n/a
45	chr5:80060102-80060152	NHDF-neo	bronchial:	n/a
46	chr5:80060102-80060152	AG04450	lung:	fetal
47	chr5:80050837-80050887	HL-60	blood:	n/a
48	chr5:80050837-80050887	HRPEpiC	eye:	n/a
49	chr5:80050837-80050887	RPTEC	kidney:	n/a
50	chr5:80060102-80060152	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:80056947..80059592-chr5:80063544..80065050,2	K562	blood:
2	chr5:80054862..80056690-chr5:80066589..80069337,2	MCF-7	breast:
3	chr5:80062757..80064804-chr5:80065865..80067964,2	K562	blood:
4	chr5:80056947..80059592-chr5:80063544..80065050,2	K562	blood:
5	chr5:80049158..80052845-chr5:80056288..80059425,3	K562	blood:
6	chr5:80048062..80050226-chr5:80052118..80053918,2	MCF-7	breast:
7	chr5:80056999..80059989-chr5:80180309..80182512,2	K562	blood:
8	chr5:80062757..80064414-chr5:80065865..80068084,2	K562	blood:
9	chr5:80049158..80052845-chr5:80056288..80059425,3	K562	blood:
10	chr5:80048062..80050226-chr5:80052118..80053918,2	MCF-7	breast:
11	chr5:80062757..80064414-chr5:80065865..80068084,2	K562	blood:
12	chr5:80062757..80064804-chr5:80065865..80067964,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000248967	TF binding region
ENSG00000248967	CpG island

Extended variants
information (count: 795 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6151759	chr5:80043404-80043405	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201262190	chr5:80043461-80043462	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs139208889	chr5:80043493-80043494	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs533081708	chr5:80043506-80043507	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369507679	chr5:80043517-80043518	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs184068830	chr5:80043528-80043529	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs563504437	chr5:80043549-80043550	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs528933304	chr5:80043571-80043572	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs75710098	chr5:80043592-80043593	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs377628840	chr5:80043651-80043652	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs373211316	chr5:80043679-80043680	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs545416647	chr5:80043695-80043696	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs145282153	chr5:80043890-80043891	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147141231	chr5:80043902-80043903	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551422768	chr5:80043912-80043913	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140255015	chr5:80043932-80043933	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570228106	chr5:80043945-80043946	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369698757	chr5:80043946-80043947	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535710844	chr5:80044001-80044002	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555427991	chr5:80044084-80044085	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144352434	chr5:80044124-80044125	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539900984	chr5:80044243-80044244	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534672184	chr5:80044246-80044247	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570731618	chr5:80044253-80044254	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78857565	chr5:80044315-80044316	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559537332	chr5:80044403-80044404	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539305801	chr5:80044440-80044441	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189959902	chr5:80044459-80044460	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576785893	chr5:80044460-80044461	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577473696	chr5:80044493-80044494	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543701577	chr5:80044494-80044495	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549767712	chr5:80044499-80044500	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180808335	chr5:80044500-80044501	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375370347	chr5:80044511-80044512	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541851299	chr5:80044539-80044540	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574736667	chr5:80044541-80044542	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs58926646	chr5:80044543-80044544	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56360314	chr5:80044547-80044548	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397998349	chr5:80044549-80044550	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112511682	chr5:80044551-80044552	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145512451	chr5:80044567-80044568	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186252967	chr5:80044616-80044617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535427153	chr5:80044620-80044621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528215975	chr5:80044638-80044639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190367251	chr5:80044736-80044737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7711263	chr5:80044789-80044790	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs572167900	chr5:80044827-80044828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376409093	chr5:80044913-80044914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148778605	chr5:80044950-80044951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142396579	chr5:80044953-80044954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	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
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
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79964800-80057800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:79971800-80112400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr5:79985000-80100600	Weak transcription	Brain Germinal Matrix	brain
4	chr5:79998600-80051000	Weak transcription	Fetal Brain Male	brain
5	chr5:79998800-80109400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr5:80004000-80050400	Weak transcription	NHDF-Ad	bronchial
7	chr5:80016200-80043600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr5:80016400-80050800	Weak transcription	Psoas Muscle	Psoas
9	chr5:80020200-80043600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr5:80022800-80051200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr5:80024200-80046800	Weak transcription	Brain Angular Gyrus	brain
12	chr5:80032400-80045400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr5:80032800-80043600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr5:80033200-80051400	Weak transcription	HMEC	breast
15	chr5:80034200-80049400	Strong transcription	Primary T cells from cord blood	blood
16	chr5:80034800-80050600	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr5:80035000-80050400	Weak transcription	Stomach Mucosa	stomach
18	chr5:80036400-80043800	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr5:80037200-80049800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr5:80037200-80050600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr5:80037400-80045800	Strong transcription	Liver	Liver
22	chr5:80037400-80049000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:80037400-80050600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr5:80037600-80044000	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr5:80037600-80049000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr5:80037600-80050200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr5:80038200-80044400	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr5:80038400-80043600	Strong transcription	Stomach Smooth Muscle	stomach
29	chr5:80038400-80044000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:80038400-80044200	Strong transcription	Primary B cells from peripheral blood	blood
31	chr5:80038400-80045800	Strong transcription	Adipose Nuclei	Adipose
32	chr5:80039200-80045000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr5:80039200-80050200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr5:80039200-80051200	Weak transcription	Colonic Mucosa	Colon
35	chr5:80039200-80075800	Weak transcription	HepG2	liver
36	chr5:80039400-80060200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr5:80039600-80043600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr5:80039600-80043800	Strong transcription	Dnd41	blood
39	chr5:80040000-80043600	Strong transcription	K562	blood
40	chr5:80040000-80044000	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr5:80040200-80073800	Weak transcription	Hela-S3	cervix
42	chr5:80040400-80044000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr5:80040400-80044200	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr5:80040400-80048600	Strong transcription	Primary B cells from cord blood	blood
45	chr5:80040600-80043800	Strong transcription	Brain Hippocampus Middle	brain
46	chr5:80040600-80044000	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr5:80040600-80044000	Strong transcription	Brain Anterior Caudate	brain
48	chr5:80040600-80044200	Strong transcription	Duodenum Mucosa	Duodenum
49	chr5:80040600-80044200	Strong transcription	Left Ventricle	heart
50	chr5:80040600-80044200	Strong transcription	Rectal Mucosa Donor 31	rectum

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