Variant report

Variant	nsv1022129
Chromosome Location	chr8:4619724-4688555
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:245)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:4668991-4669179	HepG2	liver:	n/a	chr8:4669056-4669067
2	CHD2	chr8:4644622-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD2	chr8:4654890-4654920	HepG2	liver:	n/a	n/a
4	CTCF	chr8:4644600-4644750	GM12866	blood:	n/a	n/a
5	CTCF	chr8:4644658-4644814	Gliobla	brain:	n/a	n/a
6	CTCF	chr8:4644540-4644690	HFF-Myc	foreskin:	n/a	n/a
7	CTCF	chr8:4644680-4644830	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr8:4644660-4644810	K562	blood:	n/a	n/a
9	CTCF	chr8:4644620-4644770	NB4	blood:	n/a	n/a
10	CTCF	chr8:4644660-4644810	GM12866	blood:	n/a	n/a
11	CTCF	chr8:4644640-4644790	GM12874	blood:	n/a	n/a
12	CTCF	chr8:4644640-4644790	GM12872	blood:	n/a	n/a
13	CTCF	chr8:4644625-4644807	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr8:4644600-4644750	GM12873	blood:	n/a	n/a
15	CTCF	chr8:4644647-4644651	HepG2	liver:	n/a	n/a
16	CTCF	chr8:4644580-4644730	A549	lung:	n/a	n/a
17	CTCF	chr8:4650026-4650077	ProgFib	skin:	n/a	n/a
18	CTCF	chr8:4644700-4644850	HRE	kidney:	n/a	n/a
19	CTCF	chr8:4632207-4632286	Lung_OC	lung:	n/a	n/a
20	CTCF	chr8:4644620-4644770	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr8:4644660-4644810	GM12865	blood:	n/a	n/a
22	CTCF	chr8:4644584-4644870	K562	blood:	n/a	n/a
23	CTCF	chr8:4644600-4644750	SAEC	small airway:	n/a	n/a
24	CTCF	chr8:4644620-4644770	GM12872	blood:	n/a	n/a
25	CTCF	chr8:4644680-4644748	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr8:4644642-4644821	K562	blood:	n/a	n/a
27	CTCF	chr8:4628455-4628505	LNCaP	prostate:	n/a	n/a
28	CTCF	chr8:4644600-4644750	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr8:4644660-4644810	GM12868	blood:	n/a	n/a
30	CTCF	chr8:4644646-4644815	A549	lung:	n/a	n/a
31	CTCF	chr8:4644680-4644830	GM12871	blood:	n/a	n/a
32	CTCF	chr8:4644640-4644790	GM12865	blood:	n/a	n/a
33	CTCF	chr8:4644640-4644790	HepG2	liver:	n/a	n/a
34	CTCF	chr8:4644640-4644790	A549	lung:	n/a	n/a
35	CTCF	chr8:4644597-4644867	HepG2	liver:	n/a	n/a
36	CTCF	chr8:4644516-4644932	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr8:4644600-4644750	GM12864	blood:	n/a	n/a
38	CTCF	chr8:4644640-4644790	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr8:4644587-4644847	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr8:4644652-4644813	HepG2	liver:	n/a	n/a
41	CTCF	chr8:4644600-4644750	HEK293	kidney:	n/a	n/a
42	CTCF	chr8:4644640-4644790	GM12868	blood:	n/a	n/a
43	CTCF	chr8:4654887-4654940	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr8:4644600-4644750	GM12872	blood:	n/a	n/a
45	CTCF	chr8:4644660-4644810	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr8:4644660-4644810	HepG2	liver:	n/a	n/a
47	CTCF	chr8:4644551-4644864	K562	blood:	n/a	n/a
48	CTCF	chr8:4644591-4644910	K562	blood:	n/a	n/a
49	CTCF	chr8:4644647-4644806	GM12891	blood:	n/a	n/a
50	CTCF	chr8:4671759-4671827	ProgFib	skin:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4644739-4644789	IMR90	lung:	fetal
2	chr8:4644739-4644789	IMR90	lung:	fetal
3	chr8:4629524-4629574	GM06990	blood:	n/a
4	chr8:4637584-4637634	Jurkat	blood:	n/a
5	chr8:4629524-4629574	AG04449	skin:	fetal
6	chr8:4644739-4644789	AG04450	lung:	fetal
7	chr8:4637584-4637634	PFSK-1	brain:	n/a
8	chr8:4637584-4637634	NH-A	brain:	n/a
9	chr8:4644719-4644769	SK-N-MC	brain:	n/a
10	chr8:4637584-4637634	AoSMC	blood vessel:	n/a
11	chr8:4644719-4644769	U87	brain:	n/a
12	chr8:4644739-4644789	HRE	kidney:	n/a
13	chr8:4629524-4629574	K562	blood:	n/a
14	chr8:4644719-4644769	PANC-1	pancreas:	n/a
15	chr8:4644719-4644769	NH-A	brain:	n/a
16	chr8:4637584-4637634	BE2_C	brain:	n/a
17	chr8:4629524-4629574	SK-N-SH	brain:	n/a
18	chr8:4644719-4644769	AG04449	skin:	fetal
19	chr8:4644739-4644789	GM12878	blood:	n/a
20	chr8:4644739-4644789	BE2_C	brain:	n/a
21	chr8:4644739-4644789	AG04449	skin:	fetal
22	chr8:4644739-4644789	MCF-7	breast:	n/a
23	chr8:4644719-4644769	BE2_C	brain:	n/a
24	chr8:4644719-4644769	AG04450	lung:	fetal
25	chr8:4644739-4644789	RPTEC	kidney:	n/a
26	chr8:4637584-4637634	HRE	kidney:	n/a
27	chr8:4644739-4644789	PANC-1	pancreas:	n/a
28	chr8:4637584-4637634	HAEpiC	amniotic membrane:	n/a
29	chr8:4629524-4629574	GM12892	blood:	n/a
30	chr8:4637584-4637634	MCF10A-Er-Src	breast:	n/a
31	chr8:4629524-4629574	HNPCEpiC	eye:	n/a
32	chr8:4637584-4637634	SAEC	small airway:	n/a
33	chr8:4644739-4644789	HMEC	breast:	n/a
34	chr8:4629524-4629574	PrEC	prostate:	n/a
35	chr8:4644739-4644789	T-47D	breast:	n/a
36	chr8:4629524-4629574	HepG2	liver:	n/a
37	chr8:4637584-4637634	SK-N-SH_RA	brain:	n/a
38	chr8:4644739-4644789	HepG2	liver:	n/a
39	chr8:4644719-4644769	H1-hESC	embryonic stem cell:	embryo
40	chr8:4644739-4644789	ECC-1	luminal epithelium:	n/a
41	chr8:4637584-4637634	ProgFib	skin:	n/a
42	chr8:4644719-4644769	SK-N-SH_RA	brain:	n/a
43	chr8:4629524-4629574	HRCEpiC	kidney:	n/a
44	chr8:4637584-4637634	HEK293	kidney:	embryo
45	chr8:4637584-4637634	ovcar-3	ovarian:	n/a
46	chr8:4629524-4629574	NH-A	brain:	n/a
47	chr8:4629524-4629574	SAEC	small airway:	n/a
48	chr8:4644739-4644789	HPAEpiC	pulmonary alveolar:	n/a
49	chr8:4644739-4644789	AoSMC	blood vessel:	n/a
50	chr8:4629524-4629574	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-7	chr8:4644854-4646106	NONHSAT124751

No data

Variant related genes	Relation type
PAICSP4	TF binding region
PAICSP4	CpG island

Extended variants
information (count: 3848 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:3848 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs897826	chr8:4619724-4619725	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532937163	chr8:4619734-4619735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187781035	chr8:4619738-4619739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563423701	chr8:4619749-4619750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531735513	chr8:4619756-4619757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191590468	chr8:4619757-4619758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568558162	chr8:4619764-4619765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145967176	chr8:4619779-4619780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183628491	chr8:4619791-4619792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538670506	chr8:4619793-4619794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566324107	chr8:4619794-4619795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540030434	chr8:4619800-4619801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188164665	chr8:4619806-4619807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192871903	chr8:4619816-4619817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576611471	chr8:4619851-4619852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560281366	chr8:4619871-4619872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573908434	chr8:4619876-4619877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148650651	chr8:4619889-4619890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142117185	chr8:4619891-4619892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558253939	chr8:4619920-4619921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371158560	chr8:4619943-4619944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573564005	chr8:4619978-4619979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184493797	chr8:4619993-4619994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs578162467	chr8:4619995-4619996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111843443	chr8:4620008-4620009	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs186714101	chr8:4620069-4620070	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs191177150	chr8:4620077-4620078	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs544760456	chr8:4620089-4620090	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs551463601	chr8:4620107-4620108	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs563623497	chr8:4620108-4620109	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs78437206	chr8:4620151-4620152	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs151079446	chr8:4620154-4620155	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs184729791	chr8:4620156-4620157	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs141053691	chr8:4620162-4620163	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs367548262	chr8:4620170-4620171	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs547953717	chr8:4620171-4620172	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs189179007	chr8:4620187-4620188	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs181869354	chr8:4620195-4620196	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs560707012	chr8:4620215-4620216	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs149844845	chr8:4620237-4620238	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs570343503	chr8:4620262-4620263	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs147965407	chr8:4620266-4620267	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs74459264	chr8:4620275-4620276	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs141531718	chr8:4620290-4620291	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs147047987	chr8:4620293-4620294	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs113846782	chr8:4620298-4620299	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs531785933	chr8:4620301-4620302	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs185261981	chr8:4620321-4620322	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs556913050	chr8:4620336-4620337	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs575377272	chr8:4620346-4620347	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4619600-4620200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:4619600-4620600	Enhancers	Brain Angular Gyrus	brain
3	chr8:4619600-4621000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:4619600-4623200	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr8:4619800-4620400	Enhancers	Brain Hippocampus Middle	brain
6	chr8:4619800-4621000	Enhancers	Brain Substantia Nigra	brain
7	chr8:4620000-4620400	Enhancers	H1 Cell Line	embryonic stem cell
8	chr8:4620000-4620400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr8:4620000-4620400	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr8:4620000-4621000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:4620200-4620600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:4620200-4620600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:4620200-4620600	Active TSS	Brain Anterior Caudate	brain
14	chr8:4620200-4620800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:4620400-4620800	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr8:4620400-4621000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
17	chr8:4620400-4621800	Enhancers	Brain Cingulate Gyrus	brain
18	chr8:4620600-4621000	Enhancers	Brain Anterior Caudate	brain
19	chr8:4620600-4621800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr8:4620600-4624000	Weak transcription	Brain Angular Gyrus	brain
21	chr8:4620800-4621000	Enhancers	Brain Hippocampus Middle	brain
22	chr8:4620800-4622200	Enhancers	Brain Germinal Matrix	brain
23	chr8:4621000-4630800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr8:4621800-4625000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:4623200-4625000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr8:4624800-4625200	ZNF genes & repeats	Brain Angular Gyrus	brain
27	chr8:4625000-4625200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
28	chr8:4625000-4625400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr8:4625200-4630600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr8:4625200-4631400	Weak transcription	Brain Angular Gyrus	brain
31	chr8:4628200-4629800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr8:4629800-4630800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:4630200-4630800	Enhancers	Brain Hippocampus Middle	brain
34	chr8:4630600-4630800	Enhancers	Brain Cingulate Gyrus	brain
35	chr8:4630800-4631200	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr8:4630800-4631200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr8:4630800-4631200	Active TSS	Brain Anterior Caudate	brain
38	chr8:4630800-4631200	Active TSS	Brain Hippocampus Middle	brain
39	chr8:4630800-4631200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
40	chr8:4630800-4637000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr8:4631200-4631600	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr8:4631200-4632400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr8:4631400-4631600	Enhancers	Brain Angular Gyrus	brain
44	chr8:4631600-4638800	Weak transcription	Brain Angular Gyrus	brain
45	chr8:4632200-4632600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr8:4635800-4636800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:4636000-4636200	Enhancers	Fetal Kidney	kidney
48	chr8:4636200-4637000	Weak transcription	Fetal Kidney	kidney
49	chr8:4636600-4639000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr8:4636800-4638000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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