Variant report

Variant	esv3481253
Chromosome Location	chr8:120800792-120823847
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:74)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:74 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:120814959-120815293	Hela-S3	cervix:	n/a	chr8:120815116-120815127
2	CEBPB	chr8:120814990-120815289	A549	lung:	n/a	chr8:120815116-120815127
3	CEBPB	chr8:120814976-120815176	K562	blood:	n/a	chr8:120815116-120815127
4	CEBPB	chr8:120815004-120815300	MCF-7	breast:	n/a	chr8:120815116-120815127
5	CEBPB	chr8:120816441-120816573	IMR90	lung:	n/a	n/a
6	CEBPB	chr8:120815028-120815253	K562	blood:	n/a	chr8:120815116-120815127
7	CEBPB	chr8:120814963-120815295	HepG2	liver:	n/a	chr8:120815116-120815127
8	CEBPB	chr8:120810655-120810883	MCF-7	breast:	n/a	n/a
9	CEBPB	chr8:120814409-120814609	K562	blood:	n/a	chr8:120814450-120814461
10	CTCF	chr8:120814905-120814936	GM20000	blood:	n/a	n/a
11	CTCF	chr8:120822500-120822650	HCPEpiC	choroid plexus:	n/a	n/a
12	E2F4	chr8:120818565-120818634	MCF10A-Er-Src	breast:	n/a	n/a
13	FAM48A	chr8:120819641-120819753	GM12878	blood:	n/a	n/a
14	GATA3	chr8:120810615-120810831	SH-SY5Y	brain:	n/a	chr8:120810821-120810831
15	GATA3	chr8:120813183-120813377	SH-SY5Y	brain:	n/a	chr8:120813234-120813250 chr8:120813232-120813253
16	GATA3	chr8:120807454-120807811	SH-SY5Y	brain:	n/a	n/a
17	GATA3	chr8:120810436-120810910	MCF-7	breast:	n/a	chr8:120810821-120810831
18	IRF3	chr8:120812902-120813017	GM12878	blood:	n/a	n/a
19	MAFK	chr8:120822566-120822683	H1-hESC	embryonic stem cell:	n/a	n/a
20	MYC	chr8:120802584-120802673	MCF-7	breast:	n/a	n/a
21	NR2F2	chr8:120810439-120810904	MCF-7	breast:	n/a	n/a
22	POLR2A	chr8:120814938-120815344	K562	blood:	n/a	n/a
23	POLR2A	chr8:120819731-120819814	HepG2	liver:	n/a	n/a
24	POLR2A	chr8:120804775-120806422	K562	blood:	n/a	n/a
25	POLR2A	chr8:120816469-120816889	GM12891	blood:	n/a	n/a
26	POLR2A	chr8:120804864-120804994	K562	blood:	n/a	n/a
27	POLR2A	chr8:120815288-120815466	K562	blood:	n/a	n/a
28	POLR2A	chr8:120815970-120816104	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr8:120820653-120821863	K562	blood:	n/a	n/a
30	POLR2A	chr8:120814364-120814563	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr8:120804862-120805027	MCF-7	breast:	n/a	n/a
32	POLR2A	chr8:120803182-120803190	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr8:120815031-120815139	MCF-7	breast:	n/a	n/a
34	POLR2A	chr8:120809197-120809304	ProgFib	skin:	n/a	n/a
35	POLR2A	chr8:120806543-120806569	MCF-7	breast:	n/a	n/a
36	POLR2A	chr8:120816478-120817017	GM12878	blood:	n/a	n/a
37	POLR2A	chr8:120807902-120808051	GM12878	blood:	n/a	n/a
38	POLR2A	chr8:120804770-120805059	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr8:120805536-120805692	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr8:120815693-120815767	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr8:120814656-120814932	K562	blood:	n/a	n/a
42	POLR2A	chr8:120802531-120802678	MCF-7	breast:	n/a	n/a
43	POLR2A	chr8:120814995-120815075	K562	blood:	n/a	n/a
44	POLR2A	chr8:120816133-120817568	K562	blood:	n/a	n/a
45	POLR2A	chr8:120802576-120802655	A549	lung:	n/a	n/a
46	POLR2A	chr8:120816456-120816924	GM12892	blood:	n/a	n/a
47	POLR2A	chr8:120803101-120803133	MCF-7	breast:	n/a	n/a
48	POLR2A	chr8:120813955-120814383	K562	blood:	n/a	n/a
49	POLR2A	chr8:120802553-120802673	MCF-7	breast:	n/a	n/a
50	POLR2A	chr8:120810460-120811374	K562	blood:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:120667085..120667837-chr8:120810335..120811117,2	MCF-7	breast:
2	chr8:120814901..120817854-chr8:120818185..120821075,2	K562	blood:
3	chr8:120802211..120803960-chr8:120811769..120814577,2	MCF-7	breast:
4	chr8:120816330..120818620-chr8:120831129..120833451,2	K562	blood:
5	chr8:120792905..120795655-chr8:120801527..120803030,2	K562	blood:
6	chr8:120823042..120825540-chr8:120829195..120831554,2	K562	blood:
7	chr8:120781393..120784060-chr8:120801256..120803126,2	K562	blood:
8	chr8:120822012..120824236-chr8:120824447..120826792,2	MCF-7	breast:
9	chr8:120799253..120800987-chr8:120810493..120812679,2	K562	blood:
10	chr8:120802211..120803960-chr8:120811769..120814577,2	MCF-7	breast:
11	chr8:120814901..120817854-chr8:120818185..120821075,2	K562	blood:
12	chr8:120818928..120821201-chr8:120825168..120827262,3	K562	blood:
13	chr8:120808890..120811019-chr8:120820792..120823982,3	K562	blood:
14	chr8:120799253..120800987-chr8:120810493..120812679,2	K562	blood:

No data

Variant related genes	Relation type
TAF2	TF binding region
ENSG00000064313	chromatin interactions

Extended variants
information (count: 840 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560816678	chr8:120800832-120800833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1976575	chr8:120800858-120800859	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs549354600	chr8:120800919-120800920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567665054	chr8:120800967-120800968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531681651	chr8:120801010-120801011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201601816	chr8:120801050-120801051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140302667	chr8:120801056-120801057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149772375	chr8:120801058-120801059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374362595	chr8:120801086-120801087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373150107	chr8:120801107-120801108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368720629	chr8:120801155-120801156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371156094	chr8:120801181-120801182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367741985	chr8:120801186-120801187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547286876	chr8:120801205-120801206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185792039	chr8:120801207-120801208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536156732	chr8:120801265-120801266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554240711	chr8:120801266-120801267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576017140	chr8:120801268-120801269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112180337	chr8:120801289-120801290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188942596	chr8:120801312-120801313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181714046	chr8:120801322-120801323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578217502	chr8:120801331-120801332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545574707	chr8:120801354-120801355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149807451	chr8:120801446-120801447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377081880	chr8:120801451-120801452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560674278	chr8:120801457-120801458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115229072	chr8:120801517-120801518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576284470	chr8:120801519-120801520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543326102	chr8:120801626-120801627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561102119	chr8:120801631-120801632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187289256	chr8:120801632-120801633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7837589	chr8:120801641-120801642	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs565423652	chr8:120801646-120801647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145223731	chr8:120801650-120801651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532473501	chr8:120801666-120801667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369302091	chr8:120801693-120801694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72688292	chr8:120801698-120801699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565561785	chr8:120801706-120801707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536119889	chr8:120801734-120801735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548499388	chr8:120801747-120801748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147991452	chr8:120801798-120801799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6469846	chr8:120801805-120801806	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs558273652	chr8:120801833-120801834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147865905	chr8:120801849-120801850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140625685	chr8:120801914-120801915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200339943	chr8:120801919-120801920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534727050	chr8:120802016-120802017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112562547	chr8:120802018-120802019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377495546	chr8:120802075-120802076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572707835	chr8:120802083-120802084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	21390271	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21240255	CNVD

Chromatin state (count:779 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120742600-120812800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:120744000-120814600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:120744400-120824400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr8:120760600-120804600	Weak transcription	Psoas Muscle	Psoas
5	chr8:120761600-120800800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr8:120767200-120807400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr8:120780400-120801200	Weak transcription	Brain Substantia Nigra	brain
8	chr8:120781000-120807000	Weak transcription	Brain Angular Gyrus	brain
9	chr8:120781000-120813800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:120781200-120801000	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr8:120781200-120801400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr8:120781200-120804400	Weak transcription	Spleen	Spleen
13	chr8:120781200-120804600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr8:120781200-120807000	Weak transcription	Colon Smooth Muscle	Colon
15	chr8:120781200-120807800	Weak transcription	NHLF	lung
16	chr8:120781200-120812800	Weak transcription	Colonic Mucosa	Colon
17	chr8:120781200-120829400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:120781400-120802800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr8:120781400-120803000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:120781400-120804400	Weak transcription	Esophagus	oesophagus
21	chr8:120781400-120804600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr8:120781400-120804800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr8:120781400-120805000	Weak transcription	Gastric	stomach
24	chr8:120781400-120812800	Weak transcription	Right Ventricle	heart
25	chr8:120781400-120813800	Weak transcription	Aorta	Aorta
26	chr8:120781600-120812800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr8:120781600-120844200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr8:120783800-120804400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:120785200-120812000	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr8:120785200-120812600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:120785600-120810600	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr8:120785800-120808800	Strong transcription	Primary T helper cells fromperipheralblood	blood
33	chr8:120785800-120810400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr8:120786600-120810000	Strong transcription	Fetal Thymus	thymus
35	chr8:120787800-120801600	Weak transcription	Small Intestine	intestine
36	chr8:120788000-120802800	Weak transcription	Lung	lung
37	chr8:120788800-120805800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr8:120790800-120801600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr8:120791000-120833200	Weak transcription	Fetal Heart	heart
40	chr8:120791200-120801000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr8:120791400-120801200	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr8:120791400-120807200	Weak transcription	Fetal Brain Male	brain
43	chr8:120792000-120801800	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr8:120792200-120801400	Weak transcription	Thymus	Thymus
45	chr8:120792400-120812600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:120792800-120801400	Weak transcription	Brain Hippocampus Middle	brain
47	chr8:120792800-120801400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr8:120792800-120806800	Weak transcription	Fetal Kidney	kidney
49	chr8:120793400-120814200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr8:120793600-120800800	Weak transcription	A549	lung

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