Variant report

Variant	esv3443771
Chromosome Location	chr5:49734989-49740073
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:793)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:49736483-49736699	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr5:49736931-49737450	GM12878	blood:	n/a	chr5:49737138-49737151
3	BCLAF1	chr5:49736388-49736834	GM12878	blood:	n/a	chr5:49736623-49736631
4	BHLHE40	chr5:49736550-49736771	GM12878	blood:	n/a	chr5:49736723-49736739
5	CEBPB	chr5:49736541-49736700	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr5:49736399-49736779	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr5:49736461-49736643	GM12878	blood:	n/a	n/a
8	CHD2	chr5:49736550-49736624	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr5:49737224-49737340	GM12878	blood:	n/a	n/a
10	CHD2	chr5:49737031-49737356	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr5:49736508-49736795	GM12878	blood:	n/a	n/a
12	CTCF	chr5:49736600-49736750	HEK293	kidney:	n/a	n/a
13	CTCF	chr5:49736407-49736820	GM12878	blood:	n/a	n/a
14	CTCF	chr5:49736560-49736710	HL-60	blood:	n/a	n/a
15	CTCF	chr5:49736832-49736849	GM19239	blood:	n/a	n/a
16	CTCF	chr5:49736508-49736740	MCF-7	breast:	n/a	n/a
17	CTCF	chr5:49736580-49736730	GM06990	blood:	n/a	n/a
18	CTCF	chr5:49736540-49736690	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr5:49736520-49736670	GM12869	blood:	n/a	n/a
20	CTCF	chr5:49736534-49736713	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr5:49736500-49736650	GM12865	blood:	n/a	n/a
22	CTCF	chr5:49736520-49736707	GM10266	blood:	n/a	n/a
23	CTCF	chr5:49736606-49736637	Medullo	brain:	n/a	n/a
24	CTCF	chr5:49736890-49736961	GM12892	blood:	n/a	n/a
25	CTCF	chr5:49737120-49737270	HMEC	breast:	n/a	chr5:49737208-49737221
26	CTCF	chr5:49736520-49736670	GM12875	blood:	n/a	n/a
27	CTCF	chr5:49736540-49736690	HCT-116	colon:	n/a	n/a
28	CTCF	chr5:49736498-49736821	GM19239	blood:	n/a	n/a
29	CTCF	chr5:49736480-49736630	HMEC	breast:	n/a	n/a
30	CTCF	chr5:49736580-49736730	GM12871	blood:	n/a	n/a
31	CTCF	chr5:49736479-49736672	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr5:49736480-49736630	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:49736560-49736710	AG09319	gingival:	n/a	n/a
34	CTCF	chr5:49736560-49736710	NHEK	skin:	n/a	n/a
35	CTCF	chr5:49736540-49736690	GM12865	blood:	n/a	n/a
36	CTCF	chr5:49736560-49736710	GM12869	blood:	n/a	n/a
37	CTCF	chr5:49736520-49736670	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr5:49736540-49736690	AG04449	skin:	n/a	n/a
39	CTCF	chr5:49736882-49736887	GM19240	blood:	n/a	n/a
40	CTCF	chr5:49736518-49736760	NHEK	skin:	n/a	n/a
41	CTCF	chr5:49736520-49736670	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr5:49736768-49736820	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr5:49736520-49736670	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr5:49736540-49736690	HCFaa	heart:	n/a	n/a
45	CTCF	chr5:49736560-49736710	GM12878	blood:	n/a	n/a
46	CTCF	chr5:49737520-49737670	SAEC	small airway:	n/a	n/a
47	CTCF	chr5:49736540-49736690	GM12874	blood:	n/a	n/a
48	CTCF	chr5:49736540-49736690	GM12878	blood:	n/a	n/a
49	CTCF	chr5:49736540-49736690	SAEC	small airway:	n/a	n/a
50	CTCF	chr5:49736600-49736750	Caco-2	colon:	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	chr5:49737349-49737399	AG10803	skin:	n/a
2	chr5:49737336-49737386	SK-N-SH_RA	brain:	n/a
3	chr5:49737336-49737386	HRCEpiC	kidney:	n/a
4	chr5:49739158-49739208	NT2-D1	testis:	n/a
5	chr5:49737336-49737386	Jurkat	blood:	n/a
6	chr5:49737182-49737232	NHBE	bronchial:	n/a
7	chr5:49737336-49737386	PFSK-1	brain:	n/a
8	chr5:49736085-49736135	NB4	blood:	n/a
9	chr5:49739158-49739208	NB4	blood:	n/a
10	chr5:49737336-49737386	GM06990	blood:	n/a
11	chr5:49739158-49739208	HL-60	blood:	n/a
12	chr5:49737178-49737228	AG09309	skin:	n/a
13	chr5:49738016-49738066	GM12892	blood:	n/a
14	chr5:49736664-49736714	H1-hESC	embryonic stem cell:	embryo
15	chr5:49737236-49737286	IMR90	lung:	fetal
16	chr5:49738016-49738066	NT2-D1	testis:	n/a
17	chr5:49736671-49736721	SKMC	muscle:	n/a
18	chr5:49736671-49736721	NHDF-neo	bronchial:	n/a
19	chr5:49736085-49736135	HRPEpiC	eye:	n/a
20	chr5:49737773-49737823	HEEpiC	esophagus:	n/a
21	chr5:49737178-49737228	SKMC	muscle:	n/a
22	chr5:49736664-49736714	Caco-2	colon:	n/a
23	chr5:49737236-49737286	H1-hESC	embryonic stem cell:	embryo
24	chr5:49739158-49739208	HRPEpiC	eye:	n/a
25	chr5:49739158-49739208	T-47D	breast:	n/a
26	chr5:49736988-49737038	MCF-7	breast:	n/a
27	chr5:49739158-49739208	GM12878	blood:	n/a
28	chr5:49737182-49737232	RPTEC	kidney:	n/a
29	chr5:49737336-49737386	HepG2	liver:	n/a
30	chr5:49737349-49737399	NB4	blood:	n/a
31	chr5:49737182-49737232	SKMC	muscle:	n/a
32	chr5:49737178-49737228	GM12878	blood:	n/a
33	chr5:49737773-49737823	HAEpiC	amniotic membrane:	n/a
34	chr5:49737773-49737823	MCF-7	breast:	n/a
35	chr5:49737236-49737286	HCPEpiC	choroid plexus:	n/a
36	chr5:49736988-49737038	HRE	kidney:	n/a
37	chr5:49736085-49736135	MCF10A-Er-Src	breast:	n/a
38	chr5:49737492-49737542	ProgFib	skin:	n/a
39	chr5:49737336-49737386	AG04449	skin:	fetal
40	chr5:49736671-49736721	HCT-116	colon:	n/a
41	chr5:49736671-49736721	RPTEC	kidney:	n/a
42	chr5:49736988-49737038	SK-N-MC	brain:	n/a
43	chr5:49737182-49737232	BE2_C	brain:	n/a
44	chr5:49736671-49736721	NH-A	brain:	n/a
45	chr5:49737178-49737228	HCM	heart:	n/a
46	chr5:49737178-49737228	Caco-2	colon:	n/a
47	chr5:49737182-49737232	HPAEpiC	pulmonary alveolar:	n/a
48	chr5:49737236-49737286	GM12891	blood:	n/a
49	chr5:49738016-49738066	NB4	blood:	n/a
50	chr5:49737349-49737399	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:49736414..49737923-chr5:49740071..49742726,2	MCF-7	breast:
2	chr12:89745796..89746719-chr5:49736950..49737765,2	NB4	blood:
3	chr5:49731051..49732867-chr5:49733750..49736731,2	MCF-7	breast:

No data

Variant related genes	Relation type
EMB	TF binding region
EMB	CpG island
ENSG00000170571	chromatin interactions
ENSG00000139318	chromatin interactions

Extended variants
information (count: 199 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:199 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542866795	chr5:49735076-49735077	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs188798031	chr5:49735086-49735087	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs55639144	chr5:49735109-49735110	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs553132326	chr5:49735156-49735157	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs532101989	chr5:49735245-49735246	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs544816943	chr5:49735269-49735270	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs374281936	chr5:49735296-49735297	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs373067302	chr5:49735322-49735323	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs397884028	chr5:49735323-49735324	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs144295147	chr5:49735339-49735340	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs60745446	chr5:49735340-49735341	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs564223565	chr5:49735346-49735347	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs533276664	chr5:49735354-49735355	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs28661824	chr5:49735370-49735371	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs192638677	chr5:49735475-49735476	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs28445612	chr5:49735510-49735511	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs184131431	chr5:49735542-49735543	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs115874329	chr5:49735729-49735730	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs549609518	chr5:49735767-49735768	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs188579826	chr5:49735807-49735808	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs535185111	chr5:49735809-49735810	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs558424930	chr5:49735842-49735843	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs116590738	chr5:49735844-49735845	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs180677843	chr5:49735863-49735864	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs528674368	chr5:49735877-49735878	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs557101638	chr5:49735907-49735908	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs573532760	chr5:49735920-49735921	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs201108935	chr5:49735948-49735949	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs542280164	chr5:49736011-49736012	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs114399247	chr5:49736019-49736020	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs374478011	chr5:49736042-49736043	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs183689769	chr5:49736085-49736086	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs148674387	chr5:49736092-49736093	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs189183215	chr5:49736119-49736120	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs142157413	chr5:49736140-49736141	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs564782399	chr5:49736142-49736143	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs533244673	chr5:49736144-49736145	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs543472998	chr5:49736153-49736154	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs563635758	chr5:49736166-49736167	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs61657013	chr5:49736171-49736172	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs549124706	chr5:49736244-49736245	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs566348724	chr5:49736281-49736282	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs528822867	chr5:49736304-49736305	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs182518405	chr5:49736316-49736317	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs147910527	chr5:49736323-49736324	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs71612354	chr5:49736368-49736369	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs70972912	chr5:49736388-49736389	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs186648340	chr5:49736442-49736443	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs550621593	chr5:49736443-49736444	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs567262583	chr5:49736456-49736457	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	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
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:49720400-49736400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:49720400-49736400	Weak transcription	Spleen	Spleen
3	chr5:49723600-49735200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr5:49724200-49735800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:49726400-49735000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr5:49727200-49736000	Weak transcription	HSMM	muscle
7	chr5:49727400-49735000	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr5:49727400-49735200	Weak transcription	Fetal Thymus	thymus
9	chr5:49727600-49735000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:49727600-49735800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr5:49727800-49736400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr5:49728000-49735800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:49728200-49736000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr5:49728600-49735200	Weak transcription	NHEK	skin
15	chr5:49729200-49735000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr5:49730000-49735000	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr5:49730400-49735000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:49730600-49735200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr5:49731400-49735000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr5:49731400-49735000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr5:49731400-49735200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr5:49731400-49735200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr5:49731400-49735400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr5:49731400-49735600	Weak transcription	Thymus	Thymus
25	chr5:49731600-49736000	Weak transcription	Small Intestine	intestine
26	chr5:49731800-49736000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr5:49732400-49735000	Weak transcription	Primary T cells from cord blood	blood
28	chr5:49732600-49735200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr5:49733000-49735200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr5:49733200-49735000	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr5:49733200-49735000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr5:49733200-49735000	Enhancers	Dnd41	blood
33	chr5:49733200-49735200	Weak transcription	Primary B cells from peripheral blood	blood
34	chr5:49733400-49735000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr5:49734000-49735200	Enhancers	Primary B cells from cord blood	blood
36	chr5:49734000-49735200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:49734200-49735000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr5:49734200-49735000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:49734400-49735000	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr5:49734600-49735000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr5:49734800-49735000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr5:49735000-49735200	Enhancers	Primary T cells from cord blood	blood
43	chr5:49735000-49735200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr5:49735000-49735200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
45	chr5:49735000-49735200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:49735000-49735600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
47	chr5:49735000-49735600	Enhancers	Primary hematopoietic stem cells	blood
48	chr5:49735000-49735800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr5:49735000-49735800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr5:49735000-49735800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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