Variant report

Variant	nsv882743
Chromosome Location	chr5:115501792-115634127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:541)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:115567073-115567351	HepG2	liver:	n/a	n/a
2	ATF1	chr5:115614176-115614178	K562	blood:	n/a	n/a
3	BACH1	chr5:115573174-115573254	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:115609200-115609492	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
5	BATF	chr5:115609206-115609493	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
6	CBX3	chr5:115511708-115512163	HCT-116	colon:	n/a	n/a
7	CBX3	chr5:115509774-115510264	HCT-116	colon:	n/a	n/a
8	CBX3	chr5:115612735-115612979	K562	blood:	n/a	n/a
9	CBX3	chr5:115612612-115613059	HCT-116	colon:	n/a	n/a
10	CBX3	chr5:115612653-115612965	K562	blood:	n/a	n/a
11	CEBPB	chr5:115615956-115616164	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:115584226-115584373	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
13	CEBPB	chr5:115511494-115511805	IMR90	lung:	n/a	chr5:115511652-115511663
14	CEBPB	chr5:115601292-115601498	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:115612611-115612811	A549	lung:	n/a	n/a
16	CEBPB	chr5:115608269-115608767	MCF-7	breast:	n/a	chr5:115608483-115608494
17	CEBPB	chr5:115584254-115584389	K562	blood:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
18	CEBPB	chr5:115511551-115511792	K562	blood:	n/a	chr5:115511652-115511663
19	CEBPB	chr5:115608311-115608872	IMR90	lung:	n/a	chr5:115608483-115608494
20	CEBPB	chr5:115608381-115608622	HepG2	liver:	n/a	chr5:115608483-115608494
21	CEBPB	chr5:115608357-115608659	A549	lung:	n/a	chr5:115608483-115608494
22	CEBPB	chr5:115608227-115608718	MCF-7	breast:	n/a	chr5:115608483-115608494
23	CEBPB	chr5:115511524-115511726	HepG2	liver:	n/a	chr5:115511652-115511663
24	CEBPB	chr5:115584119-115584488	MCF-7	breast:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
25	CEBPB	chr5:115584135-115584482	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
26	CEBPB	chr5:115632480-115632726	HepG2	liver:	n/a	n/a
27	CHD2	chr5:115608466-115608624	GM12878	blood:	n/a	n/a
28	CHD2	chr5:115609186-115609453	GM12878	blood:	n/a	n/a
29	CTCF	chr5:115608420-115608570	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr5:115624962-115625365	H1-hESC	embryonic stem cell:	n/a	chr5:115625169-115625182
31	CTCF	chr5:115633214-115633420	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:115514420-115514570	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr5:115625240-115625390	GM12873	blood:	n/a	n/a
34	CTCF	chr5:115573720-115573870	GM12874	blood:	n/a	n/a
35	CTCF	chr5:115573740-115573890	GM12869	blood:	n/a	n/a
36	CTCF	chr5:115573669-115573951	K562	blood:	n/a	n/a
37	CTCF	chr5:115573740-115573890	HAc	cerebellar:	n/a	n/a
38	CTCF	chr5:115608380-115608530	AG04449	skin:	n/a	n/a
39	CTCF	chr5:115633200-115633350	RPTEC	kidney:	n/a	n/a
40	CTCF	chr5:115573739-115573920	GM12878	blood:	n/a	n/a
41	CTCF	chr5:115625040-115625190	AG09309	skin:	n/a	chr5:115625169-115625182
42	CTCF	chr5:115608440-115608590	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr5:115573720-115573870	AG10803	skin:	n/a	n/a
44	CTCF	chr5:115573680-115573830	HFF	foreskin:	n/a	n/a
45	CTCF	chr5:115608380-115608530	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:115625129-115625224	HUVEC	blood vessel:	n/a	chr5:115625169-115625182
47	CTCF	chr5:115625040-115625190	AG09319	gingival:	n/a	chr5:115625169-115625182
48	CTCF	chr5:115573680-115573830	GM06990	blood:	n/a	n/a
49	CTCF	chr5:115573700-115573850	HEK293	kidney:	n/a	n/a
50	CTCF	chr5:115625072-115625269	MCF-7	breast:	n/a	chr5:115625169-115625182

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115599680-115599730	NHDF-neo	bronchial:	n/a
2	chr5:115599680-115599730	GM06990	blood:	n/a
3	chr5:115599680-115599730	AG09319	gingival:	n/a
4	chr5:115599680-115599730	RPTEC	kidney:	n/a
5	chr5:115599680-115599730	NH-A	brain:	n/a
6	chr5:115599680-115599730	IMR90	lung:	fetal
7	chr5:115599680-115599730	BE2_C	brain:	n/a
8	chr5:115599680-115599730	SK-N-SH	brain:	n/a
9	chr5:115599680-115599730	NHBE	bronchial:	n/a
10	chr5:115599680-115599730	HIPEpiC	eye:	n/a
11	chr5:115599680-115599730	AG10803	skin:	n/a
12	chr5:115599680-115599730	ProgFib	skin:	n/a
13	chr5:115599680-115599730	K562	blood:	n/a
14	chr5:115599680-115599730	AG09309	skin:	n/a
15	chr5:115599680-115599730	HRE	kidney:	n/a
16	chr5:115599680-115599730	HCM	heart:	n/a
17	chr5:115599680-115599730	HL-60	blood:	n/a
18	chr5:115599680-115599730	MCF10A-Er-Src	breast:	n/a
19	chr5:115599680-115599730	HRPEpiC	eye:	n/a
20	chr5:115599680-115599730	PFSK-1	brain:	n/a
21	chr5:115599680-115599730	HRCEpiC	kidney:	n/a
22	chr5:115599680-115599730	HAEpiC	amniotic membrane:	n/a
23	chr5:115599680-115599730	Jurkat	blood:	n/a
24	chr5:115599680-115599730	PrEC	prostate:	n/a
25	chr5:115599680-115599730	Caco-2	colon:	n/a
26	chr5:115599680-115599730	MCF-7	breast:	n/a
27	chr5:115599680-115599730	A549	lung:	n/a
28	chr5:115599680-115599730	HEK293	kidney:	embryo
29	chr5:115599680-115599730	AG04449	skin:	fetal
30	chr5:115599680-115599730	SKMC	muscle:	n/a
31	chr5:115599680-115599730	NB4	blood:	n/a
32	chr5:115599680-115599730	AoSMC	blood vessel:	n/a
33	chr5:115599680-115599730	Hepatocyte	liver:	n/a
34	chr5:115599680-115599730	HepG2	liver:	n/a
35	chr5:115599680-115599730	AG04450	lung:	fetal
36	chr5:115599680-115599730	CMK	blood:	n/a
37	chr5:115599680-115599730	Hela-S3	cervix:	n/a
38	chr5:115599680-115599730	LNCaP	prostate:	n/a
39	chr5:115599680-115599730	SK-N-SH_RA	brain:	n/a
40	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:115599680-115599730	HCPEpiC	choroid plexus:	n/a
42	chr5:115599680-115599730	HMEC	breast:	n/a
43	chr5:115599680-115599730	GM12878	blood:	n/a
44	chr5:115599680-115599730	NT2-D1	testis:	n/a
45	chr5:115599680-115599730	PANC-1	pancreas:	n/a
46	chr5:115599680-115599730	GM12892	blood:	n/a
47	chr5:115599680-115599730	HEEpiC	esophagus:	n/a
48	chr5:115599680-115599730	HCF	heart:	n/a
49	chr5:115599680-115599730	BJ	skin:	n/a
50	chr5:115599680-115599730	T-47D	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
2	chr5:115512590..115515778-chr5:115516651..115520258,3	MCF-7	breast:
3	chr5:115630950..115633524-chr5:115633964..115636710,2	MCF-7	breast:
4	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
5	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
6	chr5:115632385..115634405-chr5:115635053..115637473,2	K562	blood:
7	chr5:115473058..115473763-chr5:115624723..115625238,2	MCF-7	breast:
8	chr5:115523919..115526832-chr5:115553749..115555427,2	MCF-7	breast:
9	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
10	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
11	chr5:115512590..115515778-chr5:115516651..115520258,3	MCF-7	breast:
12	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
13	chr5:115523919..115526832-chr5:115553749..115555427,2	MCF-7	breast:
14	chr5:115630950..115633524-chr5:115633964..115636710,2	MCF-7	breast:
15	chr20:47537809..47538621-chr5:115628215..115629028,2	MCF-7	breast:
16	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LVRN.1-4	chr5:115632111-115632653	NONHSAT103359
2	lnc-LVRN.1-4	chr5:115633944-115634089	NONHSAT103358
3	lnc-SEMA6A-7	chr5:115553723-115553992	NONHSAT103356
4	lnc-LVRN.1-4	chr5:115628154-115628257	NONHSAT103358
5	lnc-LVRN.1-3	chr5:115549572-115550152	NONHSAT103355
6	lnc-LVRN.1-4	chr5:115633944-115634089	NONHSAT103359

No data

Variant related genes	Relation type
COMMD10	TF binding region
HMGN2P27	TF binding region
RNU6-644P	TF binding region
COMMD10	CpG island
HMGN2P27	CpG island
RNU6-644P	CpG island
ENSG00000124198	chromatin interactions
ENSG00000232916	chromatin interactions
ENSG00000212457	chromatin interactions

Extended variants
information (count: 6955 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:6955 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1567335	chr5:115501792-115501793	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181953779	chr5:115501806-115501807	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs139351843	chr5:115501813-115501814	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs375216757	chr5:115501819-115501820	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs528224839	chr5:115501824-115501825	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs150047142	chr5:115501826-115501827	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs530123531	chr5:115501837-115501838	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs144941003	chr5:115501838-115501839	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs142018003	chr5:115501839-115501840	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs5870690	chr5:115501859-115501860	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs376216510	chr5:115501862-115501863	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs3072987	chr5:115501864-115501865	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs377153451	chr5:115501865-115501866	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs200774147	chr5:115501866-115501867	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs116784544	chr5:115501889-115501890	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs552862801	chr5:115501908-115501909	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs374898989	chr5:115501918-115501919	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs138715194	chr5:115501930-115501931	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs5870691	chr5:115501931-115501932	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs33951327	chr5:115501932-115501933	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs3072991	chr5:115501933-115501934	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs144307542	chr5:115501944-115501945	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs147763849	chr5:115501945-115501946	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs3902887	chr5:115501952-115501953	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs372901771	chr5:115501959-115501960	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs567381318	chr5:115502007-115502008	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs535961547	chr5:115502017-115502018	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs72804853	chr5:115502119-115502120	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs569266351	chr5:115502121-115502122	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs186292732	chr5:115502134-115502135	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs190838136	chr5:115502170-115502171	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs386691444	chr5:115502172-115502173	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs570396527	chr5:115502204-115502205	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs571927235	chr5:115502205-115502206	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs541256777	chr5:115502223-115502224	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs181026316	chr5:115502229-115502230	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs143594969	chr5:115502230-115502231	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs7732346	chr5:115502248-115502249	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs375123227	chr5:115502250-115502251	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs577281730	chr5:115502251-115502252	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs72804855	chr5:115502252-115502253	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs185866172	chr5:115502307-115502308	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs528771666	chr5:115502308-115502309	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs57907464	chr5:115502324-115502325	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs148067920	chr5:115502352-115502353	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs140828396	chr5:115502414-115502415	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs549561547	chr5:115502416-115502417	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs150151582	chr5:115502438-115502439	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs538216082	chr5:115502444-115502445	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs191609600	chr5:115502474-115502475	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115462600-115502000	Weak transcription	Fetal Intestine Large	intestine
2	chr5:115471600-115521600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr5:115481400-115536000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr5:115484400-115510000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:115484400-115521400	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr5:115489200-115526800	Weak transcription	Pancreas	Pancrea
7	chr5:115489800-115528600	Weak transcription	Ovary	ovary
8	chr5:115490000-115524400	Weak transcription	Left Ventricle	heart
9	chr5:115492800-115504200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr5:115494000-115504400	Weak transcription	Aorta	Aorta
11	chr5:115494600-115522200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr5:115495200-115504600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr5:115495200-115521600	Weak transcription	Adipose Nuclei	Adipose
14	chr5:115495200-115524400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr5:115497400-115528800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:115498000-115502200	Weak transcription	Fetal Stomach	stomach
17	chr5:115498400-115502200	Weak transcription	Fetal Intestine Small	intestine
18	chr5:115499200-115527400	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr5:115499600-115502200	Weak transcription	Lung	lung
20	chr5:115500200-115503000	Strong transcription	Primary B cells from cord blood	blood
21	chr5:115500400-115502200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr5:115500400-115502800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr5:115500600-115502800	Strong transcription	Primary T cells from cord blood	blood
24	chr5:115501200-115501800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
25	chr5:115501200-115511600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr5:115501400-115502200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr5:115501600-115501800	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr5:115501600-115502400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:115501800-115502200	Weak transcription	Fetal Muscle Leg	muscle
30	chr5:115501800-115504600	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr5:115502000-115502200	Strong transcription	Fetal Intestine Large	intestine
32	chr5:115502200-115502400	ZNF genes & repeats	Fetal Intestine Large	intestine
33	chr5:115502200-115502400	ZNF genes & repeats	Fetal Intestine Small	intestine
34	chr5:115502200-115502400	ZNF genes & repeats	Fetal Stomach	stomach
35	chr5:115502200-115502400	ZNF genes & repeats	Lung	lung
36	chr5:115502200-115502800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr5:115502200-115502800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr5:115502200-115502800	ZNF genes & repeats	Fetal Muscle Leg	muscle
39	chr5:115502200-115508800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr5:115502400-115524400	Weak transcription	Fetal Intestine Large	intestine
41	chr5:115502400-115526400	Weak transcription	Lung	lung
42	chr5:115502800-115521600	Weak transcription	Primary T cells from cord blood	blood
43	chr5:115503000-115509200	Weak transcription	Primary B cells from cord blood	blood
44	chr5:115508000-115509600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr5:115508200-115518400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:115508400-115517600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:115508800-115509200	Enhancers	Rectal Smooth Muscle	rectum
48	chr5:115508800-115529200	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr5:115509200-115509400	ZNF genes & repeats	Primary B cells from cord blood	blood
50	chr5:115509200-115528400	Weak transcription	A549	lung

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