Variant report

Variant	nsv830461
Chromosome Location	chr5:118995462-119153291
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	chr5:119079705-119079979	K562	blood:	n/a	n/a
2	ARID3A	chr5:119079791-119079975	HepG2	liver:	n/a	n/a
3	BATF	chr5:119030048-119030274	GM12878	blood:	n/a	n/a
4	CBX3	chr5:119143704-119143991	HCT-116	colon:	n/a	n/a
5	CBX3	chr5:119087374-119087627	K562	blood:	n/a	n/a
6	CBX3	chr5:119002384-119002525	K562	blood:	n/a	n/a
7	CBX3	chr5:119002274-119002565	HCT-116	colon:	n/a	n/a
8	CEBPB	chr5:119142705-119142731	K562	blood:	n/a	n/a
9	CEBPB	chr5:119144254-119144573	A549	lung:	n/a	chr5:119144382-119144393
10	CEBPB	chr5:118995799-118996049	HepG2	liver:	n/a	chr5:118995912-118995923
11	CEBPB	chr5:119092140-119092340	K562	blood:	n/a	chr5:119092269-119092280
12	CEBPB	chr5:119011424-119011579	A549	lung:	n/a	chr5:119011499-119011510
13	CEBPB	chr5:119011346-119011639	HepG2	liver:	n/a	chr5:119011499-119011510
14	CEBPB	chr5:119011375-119011613	IMR90	lung:	n/a	chr5:119011499-119011510
15	CEBPB	chr5:119092119-119092319	HepG2	liver:	n/a	chr5:119092269-119092280
16	CEBPB	chr5:119144305-119144511	K562	blood:	n/a	chr5:119144382-119144393
17	CEBPB	chr5:119144267-119144596	MCF-7	breast:	n/a	chr5:119144382-119144393
18	CEBPB	chr5:119144298-119144435	HepG2	liver:	n/a	chr5:119144382-119144393
19	CEBPB	chr5:119144182-119144584	H1-hESC	embryonic stem cell:	n/a	chr5:119144382-119144393
20	CEBPB	chr5:119144248-119144655	A549	lung:	n/a	chr5:119144382-119144393
21	CEBPB	chr5:119144215-119144686	HepG2	liver:	n/a	chr5:119144382-119144393
22	CEBPB	chr5:119079798-119079941	HepG2	liver:	n/a	chr5:119079882-119079895
23	CEBPB	chr5:119144236-119144576	HepG2	liver:	n/a	chr5:119144382-119144393
24	CEBPB	chr5:119079719-119080035	Hela-S3	cervix:	n/a	chr5:119079882-119079895
25	CEBPB	chr5:119092111-119092387	H1-hESC	embryonic stem cell:	n/a	chr5:119092269-119092280
26	CEBPB	chr5:119079728-119080029	K562	blood:	n/a	chr5:119079882-119079895
27	CEBPB	chr5:119144232-119144558	Hela-S3	cervix:	n/a	chr5:119144382-119144393
28	CEBPD	chr5:119101541-119102026	K562	blood:	n/a	n/a
29	CTCF	chr5:119079780-119079930	MCF-7	breast:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
30	CTCF	chr5:119080467-119080727	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:119079800-119079950	K562	blood:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
32	CTCF	chr5:119079683-119079987	A549	lung:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
33	CTCF	chr5:119079760-119079910	GM12866	blood:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
34	CTCF	chr5:119079760-119079910	HCM	heart:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
35	CTCF	chr5:119079700-119079970	NHLF	lung:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
36	CTCF	chr5:119079821-119079911	MCF-7	breast:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
37	CTCF	chr5:119144291-119144389	HepG2	liver:	n/a	n/a
38	CTCF	chr5:119080598-119080678	MCF-7	breast:	n/a	n/a
39	CTCF	chr5:119095380-119095530	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:119079731-119079995	GM13977	blood:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
41	CTCF	chr5:119095360-119095510	A549	lung:	n/a	n/a
42	CTCF	chr5:119105842-119105844	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:119079815-119079945	LNCaP	prostate:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
44	CTCF	chr5:119079780-119079930	GM12872	blood:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
45	CTCF	chr5:119144135-119144435	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr5:119079780-119079930	AG09309	skin:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
47	CTCF	chr5:119079760-119079910	BE2_C	brain:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
48	CTCF	chr5:119079760-119079910	HA-sp	spinal cord:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
49	CTCF	chr5:119079820-119079970	GM12871	blood:	n/a	chr5:119079857-119079875 chr5:119079852-119079873
50	CTCF	chr5:119079760-119079910	HCT-116	colon:	n/a	chr5:119079857-119079875 chr5:119079852-119079873

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:119116329-119116379	AG09319	gingival:	n/a
2	chr5:119116179-119116229	HEK293	kidney:	embryo
3	chr5:119116179-119116229	ovcar-3	ovarian:	n/a
4	chr5:119116329-119116379	HRE	kidney:	n/a
5	chr5:119116329-119116379	AoSMC	blood vessel:	n/a
6	chr5:119116329-119116379	HCT-116	colon:	n/a
7	chr5:119116329-119116379	T-47D	breast:	n/a
8	chr5:119116329-119116379	ProgFib	skin:	n/a
9	chr5:119116179-119116229	NT2-D1	testis:	n/a
10	chr5:119116329-119116379	HCF	heart:	n/a
11	chr5:119116329-119116379	HCPEpiC	choroid plexus:	n/a
12	chr5:119116329-119116379	Jurkat	blood:	n/a
13	chr5:119116329-119116379	Hepatocyte	liver:	n/a
14	chr5:119116179-119116229	RPTEC	kidney:	n/a
15	chr5:119116179-119116229	T-47D	breast:	n/a
16	chr5:119116179-119116229	LNCaP	prostate:	n/a
17	chr5:119116179-119116229	AoSMC	blood vessel:	n/a
18	chr5:119116329-119116379	Hela-S3	cervix:	n/a
19	chr5:119116329-119116379	HNPCEpiC	eye:	n/a
20	chr5:119116329-119116379	NT2-D1	testis:	n/a
21	chr5:119116329-119116379	HMEC	breast:	n/a
22	chr5:119116329-119116379	AG04450	lung:	fetal
23	chr5:119116179-119116229	SK-N-SH_RA	brain:	n/a
24	chr5:119116329-119116379	A549	lung:	n/a
25	chr5:119116179-119116229	HRCEpiC	kidney:	n/a
26	chr5:119116179-119116229	IMR90	lung:	fetal
27	chr5:119116179-119116229	HCF	heart:	n/a
28	chr5:119116179-119116229	MCF-7	breast:	n/a
29	chr5:119116179-119116229	Caco-2	colon:	n/a
30	chr5:119116179-119116229	MCF10A-Er-Src	breast:	n/a
31	chr5:119116179-119116229	GM12878	blood:	n/a
32	chr5:119116179-119116229	Hela-S3	cervix:	n/a
33	chr5:119116329-119116379	HCM	heart:	n/a
34	chr5:119116329-119116379	ovcar-3	ovarian:	n/a
35	chr5:119116179-119116229	ProgFib	skin:	n/a
36	chr5:119116329-119116379	HRPEpiC	eye:	n/a
37	chr5:119116179-119116229	SAEC	small airway:	n/a
38	chr5:119116329-119116379	HepG2	liver:	n/a
39	chr5:119116329-119116379	NB4	blood:	n/a
40	chr5:119116329-119116379	NHDF-neo	bronchial:	n/a
41	chr5:119116179-119116229	HRE	kidney:	n/a
42	chr5:119116179-119116229	AG09309	skin:	n/a
43	chr5:119116329-119116379	HRCEpiC	kidney:	n/a
44	chr5:119116329-119116379	PrEC	prostate:	n/a
45	chr5:119116329-119116379	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:119116179-119116229	AG09319	gingival:	n/a
47	chr5:119116329-119116379	Caco-2	colon:	n/a
48	chr5:119116179-119116229	ECC-1	luminal epithelium:	n/a
49	chr5:119116329-119116379	HEK293	kidney:	embryo
50	chr5:119116329-119116379	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:118914344..118915154-chr5:119079337..119079948,2	MCF-7	breast:
2	chr10:7991136..7992090-chr5:119132393..119133207,2	MCF-7	breast:
3	chr5:118806209..118806753-chr5:119079435..119080027,2	K562	blood:
4	chr5:119093091..119095460-chr5:119099041..119101933,3	K562	blood:
5	chr5:118806633..118808561-chr5:119073564..119075972,2	MCF-7	breast:
6	chr5:118894367..118897199-chr5:119080311..119081964,2	K562	blood:
7	chr5:119082500..119084067-chr5:119086307..119088713,2	K562	blood:
8	chr5:118806455..118807257-chr5:119079374..119080361,4	MCF-7	breast:
9	chr5:118806276..118807504-chr5:119079301..119080297,7	MCF-7	breast:
10	chr5:119082500..119084067-chr5:119086307..119088713,2	K562	blood:
11	chr5:119007680..119010019-chr5:119012077..119014040,2	K562	blood:
12	chr3:62651556..62652452-chr5:119117724..119118513,2	MCF-7	breast:
13	chr5:119007680..119010019-chr5:119012077..119014040,2	K562	blood:
14	chr5:119126307..119128529-chr5:119131393..119133622,2	K562	blood:
15	chr5:118991005..118992570-chr5:118993778..118996554,2	K562	blood:
16	chr5:119126307..119128529-chr5:119131393..119133622,2	K562	blood:
17	chr5:119042499..119044624-chr5:119047745..119049345,2	K562	blood:
18	chr5:119042499..119044624-chr5:119047745..119049345,2	K562	blood:
19	chr5:119093091..119095460-chr5:119099041..119101933,3	K562	blood:

Variant related genes	Relation type
ENSG00000234259	TF binding region
ENSG00000234259	CpG island

Extended variants
information (count: 3508 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:3508 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs780427	chr5:118996218-118996219	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190017998	chr5:118996233-118996234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75940350	chr5:118996266-118996267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150743000	chr5:118996277-118996278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527766986	chr5:118996295-118996296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569623320	chr5:118996302-118996303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548507026	chr5:118996318-118996319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568596577	chr5:118996391-118996392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537368282	chr5:118996424-118996425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs137983529	chr5:118996439-118996440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182934023	chr5:118996451-118996452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117547500	chr5:118996534-118996535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149392836	chr5:118996571-118996572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573038101	chr5:118996581-118996582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115324580	chr5:118996596-118996597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555274597	chr5:118996616-118996617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575367278	chr5:118996626-118996627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114699514	chr5:118996643-118996644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558117273	chr5:118996658-118996659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185816954	chr5:118996667-118996668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139743729	chr5:118996705-118996706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568427608	chr5:118996746-118996747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560149671	chr5:118996754-118996755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17145639	chr5:118996764-118996765	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs551973898	chr5:118996777-118996778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551277254	chr5:118996788-118996789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570651244	chr5:118996816-118996817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542682766	chr5:118996873-118996874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143035690	chr5:118996908-118996909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534401362	chr5:118996951-118996952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531170835	chr5:118996963-118996964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146162629	chr5:118996992-118996993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570854428	chr5:118997060-118997061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs17405448	chr5:118997100-118997101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs192308635	chr5:118997109-118997110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77041644	chr5:118997111-118997112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs330191	chr5:118997116-118997117	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs555794471	chr5:118997132-118997133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140018431	chr5:118997162-118997163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142297200	chr5:118997172-118997173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557975746	chr5:118997174-118997175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74598591	chr5:118997182-118997183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs151262531	chr5:118997189-118997190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs330190	chr5:118997204-118997205	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs573549074	chr5:118997262-118997263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542245364	chr5:118997281-118997282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139312901	chr5:118997287-118997288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372775429	chr5:118997303-118997304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184086660	chr5:118997307-118997308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149922727	chr5:118997340-118997341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118996200-118996400	Enhancers	Pancreas	Pancrea
2	chr5:118996400-119000400	Weak transcription	Pancreas	Pancrea
3	chr5:119001800-119002400	ZNF genes & repeats	Liver	Liver
4	chr5:119015800-119016200	Enhancers	Pancreas	Pancrea
5	chr5:119015800-119016400	Enhancers	Fetal Muscle Trunk	muscle
6	chr5:119016200-119016800	ZNF genes & repeats	Pancreas	Pancrea
7	chr5:119016400-119016600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr5:119016600-119017800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr5:119016800-119017000	Weak transcription	Pancreas	Pancrea
10	chr5:119016800-119017800	Enhancers	Fetal Muscle Leg	muscle
11	chr5:119017000-119017200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:119017000-119017200	Enhancers	Fetal Muscle Trunk	muscle
13	chr5:119017000-119017200	Enhancers	Pancreas	Pancrea
14	chr5:119017000-119017800	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr5:119017200-119019400	Weak transcription	Pancreas	Pancrea
16	chr5:119017400-119017800	Enhancers	Primary B cells from peripheral blood	blood
17	chr5:119018200-119019000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:119019400-119019600	Enhancers	Pancreas	Pancrea
19	chr5:119025600-119026600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:119026000-119026400	Active TSS	H9 Cell Line	embryonic stem cell
21	chr5:119026000-119026400	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr5:119026400-119027600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr5:119026600-119027400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:119041200-119041400	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr5:119041200-119041600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:119041400-119041800	Enhancers	Colonic Mucosa	Colon
27	chr5:119041400-119041800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
28	chr5:119041600-119042200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:119041800-119042200	Weak transcription	Colonic Mucosa	Colon
30	chr5:119041800-119042200	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr5:119042000-119042200	Enhancers	Lung	lung
32	chr5:119042200-119042400	Active TSS	Colonic Mucosa	Colon
33	chr5:119042200-119042400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr5:119042200-119042400	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr5:119042200-119044200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr5:119042400-119042600	Flanking Active TSS	Colonic Mucosa	Colon
37	chr5:119042400-119042600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr5:119042400-119043600	Weak transcription	Lung	lung
39	chr5:119043600-119044200	Enhancers	Lung	lung
40	chr5:119044000-119044400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr5:119044200-119044400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:119046600-119047000	Enhancers	Right Ventricle	heart
43	chr5:119046800-119047000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:119047200-119058800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:119054200-119054600	Enhancers	Brain Anterior Caudate	brain
46	chr5:119054200-119054600	Enhancers	Brain Hippocampus Middle	brain
47	chr5:119057200-119058000	Enhancers	Fetal Intestine Large	intestine
48	chr5:119065800-119068600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:119071000-119071400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:119071400-119071800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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