Variant report

Variant	esv1797759
Chromosome Location	chr5:74973241-74984269
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	ARID3A	chr5:74974294-74974363	K562	blood:	n/a	n/a
2	ARID3A	chr5:74977101-74977345	K562	blood:	n/a	n/a
3	ARID3A	chr5:74976935-74977330	HepG2	liver:	n/a	n/a
4	BHLHE40	chr5:74976878-74977026	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:74978068-74978424	IMR90	lung:	n/a	n/a
6	CHD1	chr5:74975894-74975975	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr5:74977166-74977244	GM12878	blood:	n/a	n/a
8	CTCF	chr5:74977088-74977386	H1-hESC	embryonic stem cell:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
9	CTCF	chr5:74977016-74977484	GM12878	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
10	CTCF	chr5:74977180-74977330	HRE	kidney:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
11	CTCF	chr5:74977127-74977361	SK-N-SH_RA	brain:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
12	CTCF	chr5:74977180-74977330	GM12872	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
13	CTCF	chr5:74977150-74977422	Spleen_OC	spleen:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
14	CTCF	chr5:74977220-74977370	HUVEC	blood vessel:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
15	CTCF	chr5:74977220-74977370	HA-sp	spinal cord:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
16	CTCF	chr5:74977074-74977413	HCT-116	colon:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
17	CTCF	chr5:74977133-74977411	Medullo	brain:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
18	CTCF	chr5:74977058-74977407	MCF-7	breast:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
19	CTCF	chr5:74977260-74977410	GM12869	blood:	n/a	chr5:74977265-74977281
20	CTCF	chr5:74977220-74977370	BJ	skin:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
21	CTCF	chr5:74977260-74977410	GM12864	blood:	n/a	chr5:74977265-74977281
22	CTCF	chr5:74977262-74977343	MCF-7	breast:	n/a	chr5:74977265-74977281
23	CTCF	chr5:74977137-74977409	HCT-116	colon:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
24	CTCF	chr5:74977140-74977290	HAc	cerebellar:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
25	CTCF	chr5:74976969-74977471	IMR90	lung:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
26	CTCF	chr5:74977191-74977364	LNCaP	prostate:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
27	CTCF	chr5:74977240-74977390	GM12871	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
28	CTCF	chr5:74977200-74977350	HCPEpiC	choroid plexus:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
29	CTCF	chr5:74977200-74977350	GM12870	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
30	CTCF	chr5:74977060-74977210	GM12873	blood:	n/a	n/a
31	CTCF	chr5:74977160-74977310	GM12875	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
32	CTCF	chr5:74977932-74977979	GM20000	blood:	n/a	n/a
33	CTCF	chr5:74977260-74977410	AG04450	lung:	n/a	chr5:74977265-74977281
34	CTCF	chr5:74977117-74977386	A549	lung:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
35	CTCF	chr5:74977204-74977384	GM13976	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
36	CTCF	chr5:74977200-74977350	K562	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
37	CTCF	chr5:74977196-74977389	GM10266	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
38	CTCF	chr5:74977180-74977330	HMEC	breast:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
39	CTCF	chr5:74977180-74977330	HMF	breast:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
40	CTCF	chr5:74977136-74977426	MCF-7	breast:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
41	CTCF	chr5:74977180-74977330	MCF-7	breast:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
42	CTCF	chr5:74977220-74977370	AoAF	blood vessel:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
43	CTCF	chr5:74977200-74977350	NB4	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
44	CTCF	chr5:74977220-74977370	Hela-S3	cervix:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
45	CTCF	chr5:74977200-74977350	HRPEpiC	eye:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
46	CTCF	chr5:74977240-74977390	GM12873	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
47	CTCF	chr5:74977175-74977390	GM13977	blood:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
48	CTCF	chr5:74977260-74977410	GM12866	blood:	n/a	chr5:74977265-74977281
49	CTCF	chr5:74977240-74977390	HEEpiC	esophagus:	n/a	chr5:74977265-74977281 chr5:74977259-74977280
50	CTCF	chr5:74977100-74977250	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74978020-74978070	Hela-S3	cervix:	n/a
2	chr5:74978020-74978070	Hela-S3	cervix:	n/a
3	chr5:74978020-74978070	AG10803	skin:	n/a
4	chr5:74978020-74978070	NB4	blood:	n/a
5	chr5:74978020-74978070	HPAEpiC	pulmonary alveolar:	n/a
6	chr5:74978020-74978070	GM12891	blood:	n/a
7	chr5:74978020-74978070	LNCaP	prostate:	n/a
8	chr5:74978020-74978070	HNPCEpiC	eye:	n/a
9	chr5:74978020-74978070	PrEC	prostate:	n/a
10	chr5:74978020-74978070	AG09309	skin:	n/a
11	chr5:74978020-74978070	HIPEpiC	eye:	n/a
12	chr5:74978020-74978070	SK-N-MC	brain:	n/a
13	chr5:74978020-74978070	HCPEpiC	choroid plexus:	n/a
14	chr5:74978020-74978070	MCF-7	breast:	n/a
15	chr5:74978020-74978070	MCF10A-Er-Src	breast:	n/a
16	chr5:74978020-74978070	CMK	blood:	n/a
17	chr5:74978020-74978070	U87	brain:	n/a
18	chr5:74978020-74978070	HEK293	kidney:	embryo
19	chr5:74978020-74978070	H1-hESC	embryonic stem cell:	embryo
20	chr5:74978020-74978070	IMR90	lung:	fetal
21	chr5:74978020-74978070	HCT-116	colon:	n/a
22	chr5:74978020-74978070	HRE	kidney:	n/a
23	chr5:74978020-74978070	ProgFib	skin:	n/a
24	chr5:74978020-74978070	GM19239	blood:	n/a
25	chr5:74978020-74978070	SK-N-SH_RA	brain:	n/a
26	chr5:74978020-74978070	SKMC	muscle:	n/a
27	chr5:74978020-74978070	NH-A	brain:	n/a
28	chr5:74978020-74978070	PANC-1	pancreas:	n/a
29	chr5:74978020-74978070	HRCEpiC	kidney:	n/a
30	chr5:74978020-74978070	AoSMC	blood vessel:	n/a
31	chr5:74978020-74978070	SK-N-SH	brain:	n/a
32	chr5:74978020-74978070	AG04449	skin:	fetal
33	chr5:74978020-74978070	BJ	skin:	n/a
34	chr5:74978020-74978070	A549	lung:	n/a
35	chr5:74978020-74978070	HAEpiC	amniotic membrane:	n/a
36	chr5:74978020-74978070	HEEpiC	esophagus:	n/a
37	chr5:74978020-74978070	HCM	heart:	n/a
38	chr5:74978020-74978070	HCF	heart:	n/a
39	chr5:74978020-74978070	ECC-1	luminal epithelium:	n/a
40	chr5:74978020-74978070	Hepatocyte	liver:	n/a
41	chr5:74978020-74978070	HUVEC	blood vessel:	n/a
42	chr5:74978020-74978070	NHDF-neo	bronchial:	n/a
43	chr5:74978020-74978070	ovcar-3	ovarian:	n/a
44	chr5:74978020-74978070	K562	blood:	n/a
45	chr5:74978020-74978070	Jurkat	blood:	n/a
46	chr5:74978020-74978070	HL-60	blood:	n/a
47	chr5:74978020-74978070	NT2-D1	testis:	n/a
48	chr5:74978020-74978070	PFSK-1	brain:	n/a
49	chr5:74978020-74978070	HMEC	breast:	n/a
50	chr5:74978020-74978070	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:74972829..74974939-chr5:74988828..74991642,2	K562	blood:
2	chr5:74804046..74805995-chr5:74976601..74978123,2	K562	blood:
3	chr5:74880501..74881472-chr5:74976763..74977639,2	MCF-7	breast:
4	chr5:74967624..74970426-chr5:74970966..74973992,3	K562	blood:
5	chr5:74880200..74881111-chr5:74976869..74977697,3	MCF-7	breast:
6	chr5:74532317..74532921-chr5:74976842..74977712,2	K562	blood:
7	chr5:74969854..74971391-chr5:74974162..74975941,2	K562	blood:
8	chr5:74981038..74984120-chr5:75011699..75013859,3	K562	blood:
9	chr5:74983383..74985816-chr5:74986584..74989106,2	MCF-7	breast:

Variant related genes	Relation type
POC5	TF binding region
POC5	CpG island
ENSG00000152359	chromatin interactions
ENSG00000145700	chromatin interactions

Extended variants
information (count: 415 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181310662	chr5:74973360-74973361	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs568752067	chr5:74973371-74973372	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs534522377	chr5:74973373-74973374	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs16872760	chr5:74973405-74973406	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs577152469	chr5:74973447-74973448	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs545042490	chr5:74973459-74973460	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs199868163	chr5:74973462-74973463	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs182490705	chr5:74973463-74973464	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs558367782	chr5:74973493-74973494	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116354814	chr5:74973499-74973500	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs541780759	chr5:74973527-74973528	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs543791734	chr5:74973536-74973537	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs368639440	chr5:74973552-74973553	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs560578639	chr5:74973603-74973604	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs372638248	chr5:74973610-74973611	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs529909612	chr5:74973643-74973644	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs540173355	chr5:74973703-74973704	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs146700488	chr5:74973716-74973717	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs199500543	chr5:74973794-74973795	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs185963563	chr5:74973813-74973814	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs2303647	chr5:74973879-74973880	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs140274321	chr5:74973881-74973882	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs548578816	chr5:74973892-74973893	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs190724139	chr5:74973908-74973909	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs532239846	chr5:74973926-74973927	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs554175138	chr5:74973929-74973930	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs571173029	chr5:74973947-74973948	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs3815894	chr5:74973949-74973950	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs76296041	chr5:74973971-74973972	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs556752422	chr5:74973976-74973977	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs574973521	chr5:74973982-74973983	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs183136318	chr5:74973983-74973984	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs372832281	chr5:74974024-74974025	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs145249280	chr5:74974090-74974091	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs79339167	chr5:74974143-74974144	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs79323499	chr5:74974153-74974154	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs146411317	chr5:74974189-74974190	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs545661768	chr5:74974258-74974259	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs188989841	chr5:74974302-74974303	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs79516951	chr5:74974331-74974332	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs192097788	chr5:74974425-74974426	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs67570751	chr5:74974434-74974435	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182834020	chr5:74974437-74974438	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs397998176	chr5:74974442-74974443	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192639288	chr5:74974443-74974444	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140903452	chr5:74974454-74974455	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547813338	chr5:74974462-74974463	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2546189	chr5:74974507-74974508	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10066858	chr5:74974508-74974509	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs540155201	chr5:74974519-74974520	Weak transcription Enhancers 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
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	22355333	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74952800-74981400	Weak transcription	Psoas Muscle	Psoas
2	chr5:74961000-74976800	Weak transcription	Colon Smooth Muscle	Colon
3	chr5:74961000-74987800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:74962000-74979400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr5:74963000-74989800	Weak transcription	Esophagus	oesophagus
6	chr5:74963200-74976600	Weak transcription	HMEC	breast
7	chr5:74964800-74989400	Weak transcription	HSMMtube	muscle
8	chr5:74965000-74976600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:74965000-74977000	Weak transcription	Brain Angular Gyrus	brain
10	chr5:74965000-74978600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr5:74965000-74979800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr5:74965000-74983800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr5:74965000-74991200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr5:74965000-74998000	Weak transcription	Fetal Brain Female	brain
15	chr5:74965200-74977000	Weak transcription	NHLF	lung
16	chr5:74965200-75011800	Weak transcription	Brain Germinal Matrix	brain
17	chr5:74965400-74977000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr5:74965400-74977000	Weak transcription	NH-A	brain
19	chr5:74965400-74978000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr5:74965400-74979400	Weak transcription	Brain Anterior Caudate	brain
21	chr5:74965400-74980600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr5:74965400-74980800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:74965400-74981000	Weak transcription	Lung	lung
24	chr5:74965400-74997800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr5:74965400-75012400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:74965400-75012400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr5:74965400-75012400	Weak transcription	Right Ventricle	heart
28	chr5:74965600-74978400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:74965600-74979400	Weak transcription	Spleen	Spleen
30	chr5:74965600-74979600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:74965600-74980800	Weak transcription	Pancreas	Pancrea
32	chr5:74965600-74998200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr5:74965600-74998200	Weak transcription	Fetal Heart	heart
34	chr5:74965600-75010400	Weak transcription	Gastric	stomach
35	chr5:74965600-75011400	Weak transcription	Small Intestine	intestine
36	chr5:74965800-74973600	Weak transcription	HepG2	liver
37	chr5:74965800-74976600	Weak transcription	Osteobl	bone
38	chr5:74965800-74991800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr5:74966000-74973600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr5:74966000-74979400	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr5:74966000-74991000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr5:74966000-74998400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr5:74967200-74989600	Weak transcription	Hela-S3	cervix
44	chr5:74967400-74976800	Weak transcription	NHDF-Ad	bronchial
45	chr5:74967800-74975200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr5:74968000-74974000	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr5:74968400-74973400	Strong transcription	Dnd41	blood
48	chr5:74968400-74974200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr5:74968800-74983400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr5:74968800-74983800	Weak transcription	Placenta	Placenta

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