Variant report

Variant	nsv599695
Chromosome Location	chr5:127409804-127418738
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	chr5:127417222-127417454	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:127414869-127415032	HepG2	liver:	n/a	n/a
3	ATF2	chr5:127418549-127418898	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:127418088-127419357	GM12878	blood:	n/a	n/a
5	ATF2	chr5:127418102-127419121	GM12878	blood:	n/a	n/a
6	ATF3	chr5:127418506-127419270	A549	lung:	n/a	n/a
7	BACH1	chr5:127418258-127419789	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr5:127418106-127419277	A549	lung:	n/a	chr5:127419071-127419080
9	BCL3	chr5:127418492-127419313	GM12878	blood:	n/a	chr5:127419071-127419080 chr5:127419282-127419291
10	BCLAF1	chr5:127418436-127419783	GM12878	blood:	n/a	chr5:127419403-127419416 chr5:127419388-127419401 chr5:127419071-127419080 chr5:127419353-127419362 chr5:127419407-127419420 chr5:127419403-127419412 chr5:127419400-127419409 chr5:127419401-127419414 chr5:127419282-127419291 chr5:127419394-127419407 chr5:127419404-127419417
11	BCLAF1	chr5:127418406-127419664	GM12878	blood:	n/a	chr5:127419403-127419416 chr5:127419388-127419401 chr5:127419071-127419080 chr5:127419353-127419362 chr5:127419407-127419420 chr5:127419403-127419412 chr5:127419400-127419409 chr5:127419401-127419414 chr5:127419282-127419291 chr5:127419394-127419407 chr5:127419404-127419417
12	BHLHE40	chr5:127418273-127419774	K562	blood:	n/a	chr5:127419517-127419533 chr5:127419400-127419416 chr5:127418964-127418980 chr5:127419385-127419401 chr5:127419394-127419410 chr5:127419467-127419483 chr5:127419406-127419422 chr5:127419315-127419331
13	BHLHE40	chr5:127418520-127420157	GM12878	blood:	n/a	chr5:127419517-127419533 chr5:127419400-127419416 chr5:127418964-127418980 chr5:127419385-127419401 chr5:127419394-127419410 chr5:127419467-127419483 chr5:127419406-127419422 chr5:127419315-127419331
14	BRCA1	chr5:127418566-127419105	HepG2	liver:	n/a	chr5:127418803-127418812
15	BRCA1	chr5:127418397-127419256	GM12878	blood:	n/a	chr5:127418803-127418812
16	BRCA1	chr5:127418319-127419224	Hela-S3	cervix:	n/a	chr5:127418803-127418812
17	BRCA1	chr5:127418357-127419034	H1-hESC	embryonic stem cell:	n/a	chr5:127418803-127418812
18	CBX3	chr5:127418326-127419327	K562	blood:	n/a	n/a
19	CCNT2	chr5:127414697-127414881	K562	blood:	n/a	n/a
20	CCNT2	chr5:127418494-127420917	K562	blood:	n/a	chr5:127420429-127420438
21	CEBPB	chr5:127418261-127418955	GM12878	blood:	n/a	n/a
22	CEBPB	chr5:127418518-127418718	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:127418384-127419331	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:127410703-127410993	IMR90	lung:	n/a	n/a
25	CEBPB	chr5:127410712-127410970	A549	lung:	n/a	n/a
26	CEBPB	chr5:127410685-127411030	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:127410721-127411030	K562	blood:	n/a	n/a
28	CEBPD	chr5:127418692-127418984	HepG2	liver:	n/a	n/a
29	CHD1	chr5:127417209-127417730	GM12878	blood:	n/a	n/a
30	CHD1	chr5:127418143-127419746	GM12878	blood:	n/a	chr5:127418803-127418812
31	CHD2	chr5:127418357-127419739	H1-hESC	embryonic stem cell:	n/a	chr5:127418803-127418812
32	CHD2	chr5:127418180-127419559	K562	blood:	n/a	chr5:127418803-127418812
33	CHD2	chr5:127418430-127419625	HepG2	liver:	n/a	chr5:127418803-127418812
34	CHD2	chr5:127418261-127419994	Hela-S3	cervix:	n/a	chr5:127418803-127418812
35	CHD2	chr5:127418119-127419808	GM12878	blood:	n/a	chr5:127418803-127418812
36	CREB1	chr5:127418301-127419932	GM12878	blood:	n/a	n/a
37	CREB1	chr5:127418416-127419741	HepG2	liver:	n/a	n/a
38	CREB1	chr5:127418436-127419717	A549	lung:	n/a	n/a
39	CTBP2	chr5:127418564-127420698	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr5:127417360-127417510	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr5:127417180-127417330	GM12871	blood:	n/a	n/a
42	CTCF	chr5:127417349-127417458	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr5:127417260-127417410	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr5:127417300-127417450	GM12872	blood:	n/a	n/a
45	CTCF	chr5:127417320-127417470	Caco-2	colon:	n/a	n/a
46	CTCF	chr5:127417420-127417570	HAc	cerebellar:	n/a	n/a
47	CTCF	chr5:127417340-127417490	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr5:127417385-127417449	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr5:127417140-127417290	HMEC	breast:	n/a	n/a
50	CTCF	chr5:127417380-127417530	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:127418547-127418597	PrEC	prostate:	n/a
2	chr5:127418547-127418597	NB4	blood:	n/a
3	chr5:127416532-127416582	Jurkat	blood:	n/a
4	chr5:127418547-127418597	GM06990	blood:	n/a
5	chr5:127416532-127416582	HCT-116	colon:	n/a
6	chr5:127418547-127418597	HCF	heart:	n/a
7	chr5:127416532-127416582	T-47D	breast:	n/a
8	chr5:127418547-127418597	AG09309	skin:	n/a
9	chr5:127418547-127418597	GM12892	blood:	n/a
10	chr5:127418547-127418597	NHBE	bronchial:	n/a
11	chr5:127416532-127416582	AG09309	skin:	n/a
12	chr5:127418547-127418597	HRCEpiC	kidney:	n/a
13	chr5:127416532-127416582	HL-60	blood:	n/a
14	chr5:127416532-127416582	Hepatocyte	liver:	n/a
15	chr5:127418547-127418597	CMK	blood:	n/a
16	chr5:127416532-127416582	AG04449	skin:	fetal
17	chr5:127418547-127418597	T-47D	breast:	n/a
18	chr5:127418547-127418597	HEEpiC	esophagus:	n/a
19	chr5:127418547-127418597	GM12878	blood:	n/a
20	chr5:127418547-127418597	AG10803	skin:	n/a
21	chr5:127418547-127418597	HRE	kidney:	n/a
22	chr5:127418547-127418597	AG04449	skin:	fetal
23	chr5:127416532-127416582	SKMC	muscle:	n/a
24	chr5:127418547-127418597	ovcar-3	ovarian:	n/a
25	chr5:127418547-127418597	K562	blood:	n/a
26	chr5:127416532-127416582	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:127418547-127418597	AG09319	gingival:	n/a
28	chr5:127418547-127418597	AoSMC	blood vessel:	n/a
29	chr5:127418547-127418597	RPTEC	kidney:	n/a
30	chr5:127416532-127416582	HEK293	kidney:	embryo
31	chr5:127416532-127416582	HRPEpiC	eye:	n/a
32	chr5:127418547-127418597	IMR90	lung:	fetal
33	chr5:127418547-127418597	SK-N-MC	brain:	n/a
34	chr5:127418547-127418597	PFSK-1	brain:	n/a
35	chr5:127418547-127418597	SK-N-SH	brain:	n/a
36	chr5:127418547-127418597	A549	lung:	n/a
37	chr5:127418547-127418597	U87	brain:	n/a
38	chr5:127416532-127416582	AG10803	skin:	n/a
39	chr5:127416532-127416582	SK-N-SH_RA	brain:	n/a
40	chr5:127416532-127416582	U87	brain:	n/a
41	chr5:127418547-127418597	HL-60	blood:	n/a
42	chr5:127416532-127416582	SK-N-MC	brain:	n/a
43	chr5:127416532-127416582	H1-hESC	embryonic stem cell:	embryo
44	chr5:127418547-127418597	BE2_C	brain:	n/a
45	chr5:127418547-127418597	HEK293	kidney:	embryo
46	chr5:127418547-127418597	GM19239	blood:	n/a
47	chr5:127416532-127416582	BE2_C	brain:	n/a
48	chr5:127418547-127418597	HepG2	liver:	n/a
49	chr5:127416532-127416582	HEEpiC	esophagus:	n/a
50	chr5:127416532-127416582	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:103800274..103800891-chr5:127418277..127419237,2	Hela-S3	cervix:
2	chr5:127417788..127421083-chr5:127443681..127446699,3	K562	blood:
3	chr5:127405958..127407674-chr5:127410063..127411683,2	K562	blood:
4	chr5:127394903..127397902-chr5:127411158..127414826,3	K562	blood:
5	chr5:127410989..127412593-chr5:127415197..127417314,3	K562	blood:
6	chr5:127267836..127272333-chr5:127416528..127421531,14	MCF-7	breast:
7	chr5:127410989..127412593-chr5:127415197..127417314,3	K562	blood:
8	chr5:127400217..127401910-chr5:127408203..127411062,2	K562	blood:
9	chr20:47444082..47444633-chr5:127418681..127419323,2	Hela-S3	cervix:
10	chr5:127408566..127411442-chr5:127412168..127414357,2	K562	blood:
11	chr5:127267226..127272789-chr5:127416073..127421756,7	MCF-7	breast:
12	chr5:127418681..127419214-chr7:95063949..95064486,2	HCT-116	colon:
13	chr17:36830889..36831633-chr5:127418494..127419135,2	HCT-116	colon:
14	chr5:127404446..127408379-chr5:127410147..127413224,3	MCF-7	breast:
15	chr5:127406642..127408516-chr5:127409613..127411185,2	MCF-7	breast:
16	chr5:127408566..127411442-chr5:127412168..127414357,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBN2-2	chr5:127417665-127417886	ENSG00000245937
2	lnc-FBN2-2	chr5:127418427-127418573	ENSG00000245937
3	lnc-FBN2-2	chr5:127418427-127418652	ENSG00000245937
4	lnc-FBN2-2	chr5:127412639-127412785	ENSG00000245937
5	lnc-SLC12A2-2	chr5:127412451-127412575	NONHSAT103656
6	lnc-FBN2-2	chr5:127412639-127412785	ENSG00000245937
7	lnc-SLC12A2-2	chr5:127412709-127413364	NONHSAT103656

Variant related genes	Relation type
ENSG00000245937	TF binding region
SLC12A2	TF binding region
ENSG00000245937	CpG island
SLC12A2	CpG island
ENSG00000100664	chromatin interactions
ENSG00000250329	chromatin interactions
ENSG00000230561	chromatin interactions
ENSG00000124126	chromatin interactions
ENSG00000105854	chromatin interactions
ENSG00000179294	chromatin interactions
KIAA0802	miRNA target sites
EDNRA	miRNA target sites
ZFP36L2	miRNA target sites
LAPTM4B	miRNA target sites
INCENP	miRNA target sites

Extended variants
information (count: 244 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:244 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527587770	chr5:127409819-127409820	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs541188151	chr5:127409998-127409999	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs373979132	chr5:127410057-127410058	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs572931407	chr5:127410103-127410104	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs535222747	chr5:127410104-127410105	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs188497405	chr5:127410234-127410235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72792292	chr5:127410235-127410236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376420714	chr5:127410237-127410238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368766654	chr5:127410242-127410243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563687570	chr5:127410423-127410424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11749028	chr5:127410465-127410466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192909227	chr5:127410478-127410479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11949446	chr5:127410505-127410506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534998761	chr5:127410525-127410526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377631275	chr5:127410534-127410535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551922334	chr5:127410690-127410691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369895385	chr5:127410705-127410706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548294786	chr5:127410733-127410734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76208917	chr5:127410745-127410746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556025184	chr5:127410993-127410994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576105241	chr5:127411020-127411021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535393986	chr5:127411028-127411029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564621354	chr5:127411072-127411073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564258152	chr5:127411146-127411147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572336521	chr5:127411309-127411310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572072415	chr5:127411310-127411311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146343757	chr5:127411335-127411336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564285756	chr5:127411360-127411361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183153969	chr5:127411404-127411405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188039005	chr5:127411410-127411411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10045307	chr5:127411454-127411455	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529353787	chr5:127411486-127411487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548929883	chr5:127411487-127411488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373436785	chr5:127411537-127411538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6595800	chr5:127411647-127411648	Weak transcription Strong transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs528737608	chr5:127411696-127411697	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs191358162	chr5:127411698-127411699	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs551822021	chr5:127411732-127411733	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs571801504	chr5:127411791-127411792	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs537293976	chr5:127411818-127411819	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs551157045	chr5:127411855-127411856	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs568421473	chr5:127411922-127411923	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs569728999	chr5:127411995-127411996	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs535560308	chr5:127412043-127412044	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs115523726	chr5:127412113-127412114	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs114464208	chr5:127412144-127412145	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs183890038	chr5:127412168-127412169	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs1432613	chr5:127412233-127412234	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs528436850	chr5:127412267-127412268	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs114563410	chr5:127412299-127412300	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD

Chromatin state (count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127333600-127417800	Weak transcription	Pancreas	Pancrea
2	chr5:127356400-127414000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr5:127374600-127418000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr5:127375200-127414400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr5:127376400-127414400	Weak transcription	Dnd41	blood
6	chr5:127377200-127414200	Weak transcription	K562	blood
7	chr5:127378000-127416600	Weak transcription	Spleen	Spleen
8	chr5:127378400-127414200	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr5:127378800-127415800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr5:127379000-127417400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr5:127380200-127414600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr5:127380200-127416200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr5:127386400-127414400	Weak transcription	Colon Smooth Muscle	Colon
14	chr5:127386600-127417000	Weak transcription	Adipose Nuclei	Adipose
15	chr5:127389200-127414400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr5:127389400-127414600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr5:127389600-127417000	Weak transcription	Fetal Heart	heart
18	chr5:127389800-127416200	Weak transcription	Thymus	Thymus
19	chr5:127390200-127415400	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr5:127390200-127417600	Weak transcription	Psoas Muscle	Psoas
21	chr5:127390400-127414200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr5:127390400-127416600	Weak transcription	Fetal Stomach	stomach
23	chr5:127390600-127415000	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr5:127391000-127417600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr5:127391200-127414400	Weak transcription	A549	lung
26	chr5:127391400-127414800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr5:127391400-127416600	Weak transcription	Fetal Muscle Leg	muscle
28	chr5:127392200-127414400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr5:127394200-127418000	Weak transcription	Lung	lung
30	chr5:127394600-127416800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr5:127396000-127417000	Weak transcription	Ovary	ovary
32	chr5:127396200-127416200	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr5:127396400-127413000	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr5:127396400-127414400	Weak transcription	Primary T cells from cord blood	blood
35	chr5:127398200-127416200	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr5:127398400-127414400	Weak transcription	NHDF-Ad	bronchial
37	chr5:127398400-127414600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:127398400-127415800	Weak transcription	Rectal Smooth Muscle	rectum
39	chr5:127398400-127416200	Weak transcription	HSMMtube	muscle
40	chr5:127398400-127417400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr5:127398600-127414400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:127398600-127416600	Weak transcription	Osteobl	bone
43	chr5:127399000-127412400	Weak transcription	HMEC	breast
44	chr5:127399000-127413000	Weak transcription	Small Intestine	intestine
45	chr5:127399000-127414400	Weak transcription	Brain Angular Gyrus	brain
46	chr5:127399000-127414400	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr5:127399000-127415600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr5:127399000-127417400	Weak transcription	HSMM	muscle
49	chr5:127399200-127412400	Weak transcription	NHEK	skin
50	chr5:127399200-127414400	Weak transcription	Brain Hippocampus Middle	brain

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