Variant report

Variant	nsv831312
Chromosome Location	chr8:51239772-51422844
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	chr8:51351100-51351279	HepG2	liver:	n/a	n/a
2	ATF3	chr8:51310742-51311085	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr8:51310791-51311060	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr8:51310845-51311121	K562	blood:	n/a	n/a
5	BACH1	chr8:51322783-51322854	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:51360829-51360868	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:51380375-51380444	K562	blood:	n/a	n/a
8	BHLHE40	chr8:51310789-51311051	HepG2	liver:	n/a	n/a
9	BHLHE40	chr8:51310826-51311066	K562	blood:	n/a	n/a
10	BRCA1	chr8:51310893-51310975	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:51306303-51306556	IMR90	lung:	n/a	chr8:51306433-51306444
12	CEBPB	chr8:51340868-51341197	IMR90	lung:	n/a	chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341046-51341057 chr8:51341047-51341056 chr8:51341045-51341056
13	CEBPB	chr8:51310785-51311128	K562	blood:	n/a	chr8:51310953-51310964
14	CEBPB	chr8:51310785-51311240	MCF-7	breast:	n/a	chr8:51310953-51310964
15	CEBPB	chr8:51330359-51330662	A549	lung:	n/a	chr8:51330522-51330533
16	CEBPB	chr8:51301753-51301900	K562	blood:	n/a	chr8:51301857-51301868
17	CEBPB	chr8:51417321-51417664	Hela-S3	cervix:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
18	CEBPB	chr8:51388326-51388344	A549	lung:	n/a	n/a
19	CEBPB	chr8:51340880-51341177	HepG2	liver:	n/a	chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341046-51341057 chr8:51341047-51341056 chr8:51341045-51341056
20	CEBPB	chr8:51306294-51306472	A549	lung:	n/a	chr8:51306433-51306444
21	CEBPB	chr8:51417301-51417674	HepG2	liver:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
22	CEBPB	chr8:51301717-51302010	HepG2	liver:	n/a	chr8:51301857-51301868
23	CEBPB	chr8:51310815-51311070	A549	lung:	n/a	chr8:51310953-51310964
24	CEBPB	chr8:51340892-51341151	H1-hESC	embryonic stem cell:	n/a	chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341046-51341057 chr8:51341047-51341056 chr8:51341045-51341056
25	CEBPB	chr8:51281995-51282207	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:51330470-51330673	H1-hESC	embryonic stem cell:	n/a	chr8:51330522-51330533
27	CEBPB	chr8:51417365-51417636	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
28	CEBPB	chr8:51330385-51330704	IMR90	lung:	n/a	chr8:51330522-51330533
29	CEBPB	chr8:51320425-51320659	HepG2	liver:	n/a	chr8:51320549-51320560
30	CEBPB	chr8:51293479-51293710	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:51310770-51311151	H1-hESC	embryonic stem cell:	n/a	chr8:51310953-51310964
32	CEBPB	chr8:51417303-51417661	K562	blood:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
33	CEBPB	chr8:51284262-51284449	A549	lung:	n/a	n/a
34	CEBPB	chr8:51310770-51311130	HepG2	liver:	n/a	chr8:51310953-51310964
35	CEBPB	chr8:51293521-51293731	A549	lung:	n/a	n/a
36	CEBPB	chr8:51417307-51417674	H1-hESC	embryonic stem cell:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
37	CEBPB	chr8:51417299-51417672	IMR90	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
38	CEBPB	chr8:51310763-51311140	IMR90	lung:	n/a	chr8:51310953-51310964
39	CEBPB	chr8:51295153-51295450	A549	lung:	n/a	chr8:51295254-51295263 chr8:51295252-51295263 chr8:51295254-51295265
40	CEBPB	chr8:51417314-51417678	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
41	CEBPB	chr8:51384894-51385137	IMR90	lung:	n/a	n/a
42	CEBPB	chr8:51310744-51311162	MCF-7	breast:	n/a	chr8:51310953-51310964
43	CEBPB	chr8:51306357-51306493	HepG2	liver:	n/a	chr8:51306433-51306444
44	CEBPB	chr8:51295240-51295364	HepG2	liver:	n/a	chr8:51295254-51295263 chr8:51295252-51295263 chr8:51295254-51295265
45	CEBPB	chr8:51330350-51330820	HepG2	liver:	n/a	chr8:51330522-51330533
46	CEBPB	chr8:51379026-51379129	A549	lung:	n/a	n/a
47	CHD2	chr8:51310792-51311032	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr8:51310806-51311012	Medullo	brain:	n/a	n/a
49	CTCF	chr8:51310820-51310970	GM12866	blood:	n/a	n/a
50	CTCF	chr8:51310900-51311050	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:51404066-51404116	SKMC	muscle:	n/a
2	chr8:51404179-51404229	HUVEC	blood vessel:	n/a
3	chr8:51404179-51404229	T-47D	breast:	n/a
4	chr8:51288552-51288602	SK-N-SH	brain:	n/a
5	chr8:51404106-51404156	HepG2	liver:	n/a
6	chr8:51404106-51404156	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:51404106-51404156	GM19239	blood:	n/a
8	chr8:51364244-51364294	NHBE	bronchial:	n/a
9	chr8:51364244-51364294	NH-A	brain:	n/a
10	chr8:51404179-51404229	HL-60	blood:	n/a
11	chr8:51404066-51404116	AG09309	skin:	n/a
12	chr8:51364244-51364294	LNCaP	prostate:	n/a
13	chr8:51404066-51404116	U87	brain:	n/a
14	chr8:51288552-51288602	AG04449	skin:	fetal
15	chr8:51364244-51364294	AoSMC	blood vessel:	n/a
16	chr8:51404179-51404229	ProgFib	skin:	n/a
17	chr8:51404106-51404156	U87	brain:	n/a
18	chr8:51404179-51404229	HCPEpiC	choroid plexus:	n/a
19	chr8:51404106-51404156	NH-A	brain:	n/a
20	chr8:51404179-51404229	HNPCEpiC	eye:	n/a
21	chr8:51404066-51404116	NHBE	bronchial:	n/a
22	chr8:51404066-51404116	SAEC	small airway:	n/a
23	chr8:51404179-51404229	AG09319	gingival:	n/a
24	chr8:51364244-51364294	ECC-1	luminal epithelium:	n/a
25	chr8:51364244-51364294	SKMC	muscle:	n/a
26	chr8:51404066-51404116	ECC-1	luminal epithelium:	n/a
27	chr8:51404179-51404229	GM12892	blood:	n/a
28	chr8:51404066-51404116	HCM	heart:	n/a
29	chr8:51404179-51404229	HCF	heart:	n/a
30	chr8:51404179-51404229	BJ	skin:	n/a
31	chr8:51404179-51404229	LNCaP	prostate:	n/a
32	chr8:51288552-51288602	NH-A	brain:	n/a
33	chr8:51404179-51404229	MCF10A-Er-Src	breast:	n/a
34	chr8:51404106-51404156	HUVEC	blood vessel:	n/a
35	chr8:51404179-51404229	HepG2	liver:	n/a
36	chr8:51288552-51288602	NT2-D1	testis:	n/a
37	chr8:51364244-51364294	AG10803	skin:	n/a
38	chr8:51288552-51288602	AG09319	gingival:	n/a
39	chr8:51288552-51288602	NHBE	bronchial:	n/a
40	chr8:51364244-51364294	Caco-2	colon:	n/a
41	chr8:51404106-51404156	ProgFib	skin:	n/a
42	chr8:51404066-51404116	NB4	blood:	n/a
43	chr8:51288552-51288602	HEEpiC	esophagus:	n/a
44	chr8:51404106-51404156	Hela-S3	cervix:	n/a
45	chr8:51404106-51404156	HCM	heart:	n/a
46	chr8:51404179-51404229	AG09309	skin:	n/a
47	chr8:51404106-51404156	HEK293	kidney:	embryo
48	chr8:51288552-51288602	U87	brain:	n/a
49	chr8:51404106-51404156	HNPCEpiC	eye:	n/a
50	chr8:51288552-51288602	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:51252100..51253925-chr8:51256216..51258662,2	MCF-7	breast:
2	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:
3	chr8:49891255..49891972-chr8:51310445..51311051,2	MCF-7	breast:
4	chr13:32746778..32747333-chr8:51314361..51315226,2	MCF-7	breast:
5	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:
6	chr8:50947077..50947745-chr8:51310573..51311162,2	MCF-7	breast:
7	chr8:50753724..50754320-chr8:51310816..51311345,2	MCF-7	breast:
8	chr8:50826287..50827033-chr8:51310198..51311230,3	MCF-7	breast:
9	chr8:51252100..51253925-chr8:51256216..51258662,2	MCF-7	breast:
10	chr8:50947214..50948091-chr8:51310516..51311364,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf22-6	chr8:51294466-51294835	ENSG00000253849.1
2	lnc-C8orf22-6	chr8:51293575-51293638	ENSG00000253849.1

Variant related genes	Relation type
ENSG00000254392	TF binding region
ENSG00000253849	TF binding region
SNTG1	TF binding region
ENSG00000254392	CpG island
ENSG00000253849	CpG island
SNTG1	CpG island

Extended variants
information (count: 6509 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:6509 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571413163	chr8:51239794-51239795	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs532332447	chr8:51239797-51239798	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs78936880	chr8:51239820-51239821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570080062	chr8:51239831-51239832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537397646	chr8:51239843-51239844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531071030	chr8:51239845-51239846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs193273864	chr8:51239861-51239862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184012912	chr8:51239900-51239901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149080608	chr8:51239939-51239940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs578114722	chr8:51239950-51239951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575481569	chr8:51239960-51239961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572597185	chr8:51239981-51239982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557607195	chr8:51239984-51239985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187808596	chr8:51239990-51239991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376301164	chr8:51240000-51240001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542173627	chr8:51240008-51240009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560535157	chr8:51240035-51240036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528216886	chr8:51240056-51240057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540301523	chr8:51240079-51240080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114040381	chr8:51240128-51240129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567681466	chr8:51240132-51240133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550621054	chr8:51240136-51240137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562732543	chr8:51240137-51240138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370727156	chr8:51240141-51240142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs530008583	chr8:51240205-51240206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540259271	chr8:51240219-51240220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549445702	chr8:51240259-51240260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567643757	chr8:51240277-51240278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534843650	chr8:51240282-51240283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76316865	chr8:51240291-51240292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111598847	chr8:51240294-51240295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183979254	chr8:51240343-51240344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539178130	chr8:51240347-51240348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113097370	chr8:51240430-51240431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191928202	chr8:51240436-51240437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529605433	chr8:51240453-51240454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143203843	chr8:51240471-51240472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111413865	chr8:51240523-51240524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138754081	chr8:51240525-51240526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77837400	chr8:51240539-51240540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564964923	chr8:51240611-51240612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184398390	chr8:51240612-51240613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544437620	chr8:51240623-51240624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539946386	chr8:51240627-51240628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562669349	chr8:51240708-51240709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75178824	chr8:51240709-51240710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548490555	chr8:51240718-51240719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147401143	chr8:51240734-51240735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561285451	chr8:51240741-51240742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528460493	chr8:51240766-51240767	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
22q11 deletion syndrome	20357662	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:243 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51239400-51239800	Flanking Active TSS	Liver	Liver
2	chr8:51239800-51241200	Enhancers	Liver	Liver
3	chr8:51240200-51240800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:51240800-51241200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:51241000-51242600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:51241000-51243000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
7	chr8:51241200-51241400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:51241200-51241800	Weak transcription	Liver	Liver
9	chr8:51241200-51242000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
10	chr8:51241400-51242400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr8:51241800-51242000	ZNF genes & repeats	Liver	Liver
12	chr8:51242000-51246800	Weak transcription	Liver	Liver
13	chr8:51242400-51243200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr8:51243200-51271600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr8:51246800-51247200	Enhancers	Liver	Liver
16	chr8:51247200-51249600	Weak transcription	Liver	Liver
17	chr8:51249400-51249800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr8:51249600-51250200	Enhancers	Liver	Liver
19	chr8:51262200-51262800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:51262200-51263000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr8:51263000-51264800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:51267200-51267400	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr8:51267200-51267400	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr8:51267600-51268800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr8:51267600-51269000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr8:51268800-51271600	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr8:51268800-51271800	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr8:51269000-51273800	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr8:51269400-51270000	Enhancers	Spleen	Spleen
30	chr8:51269600-51272000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr8:51270000-51270400	Weak transcription	Spleen	Spleen
32	chr8:51270400-51271800	Enhancers	Spleen	Spleen
33	chr8:51271400-51272000	Active TSS	Rectal Smooth Muscle	rectum
34	chr8:51271600-51272000	Enhancers	Fetal Intestine Large	intestine
35	chr8:51271600-51272000	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr8:51271600-51272200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:51271600-51272200	Enhancers	Fetal Intestine Small	intestine
38	chr8:51271800-51272200	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr8:51271800-51272200	Enhancers	Brain Germinal Matrix	brain
40	chr8:51271800-51275800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr8:51272000-51275400	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr8:51272000-51275800	Weak transcription	Fetal Intestine Large	intestine
43	chr8:51273800-51274200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr8:51274200-51276400	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr8:51275400-51275800	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr8:51275800-51276400	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr8:51275800-51276600	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr8:51275800-51276800	Enhancers	Fetal Intestine Large	intestine
49	chr8:51276400-51276800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
50	chr8:51276400-51276800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum

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