Variant report

Variant	nsv1031580
Chromosome Location	chr8:10316170-10334279
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	chr8:10318722-10318795	K562	blood:	n/a	n/a
2	CTCF	chr8:10331941-10332147	MCF-7	breast:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
3	CTCF	chr8:10331940-10332090	HMEC	breast:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
4	CTCF	chr8:10331954-10332129	A549	lung:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
5	CTCF	chr8:10331937-10332149	K562	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
6	CTCF	chr8:10331960-10332110	GM12865	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
7	CTCF	chr8:10328380-10328530	NHEK	skin:	n/a	n/a
8	CTCF	chr8:10331980-10332130	HEK293	kidney:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
9	CTCF	chr8:10331967-10332153	LNCaP	prostate:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
10	CTCF	chr8:10331960-10332110	SAEC	small airway:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
11	CTCF	chr8:10331980-10332130	GM12868	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
12	CTCF	chr8:10331920-10332070	A549	lung:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
13	CTCF	chr8:10331960-10332110	HepG2	liver:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
14	CTCF	chr8:10330684-10330769	ProgFib	skin:	n/a	n/a
15	CTCF	chr8:10331942-10332123	A549	lung:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
16	CTCF	chr8:10331900-10332290	MCF-7	breast:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
17	CTCF	chr8:10331880-10332030	WI-38	lung:	n/a	n/a
18	CTCF	chr8:10331940-10332090	GM12874	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
19	CTCF	chr8:10331920-10332070	MCF-7	breast:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
20	CTCF	chr8:10331935-10332165	Gliobla	brain:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
21	CTCF	chr8:10332000-10332150	AG10803	skin:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
22	CTCF	chr8:10331960-10332110	AG04450	lung:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
23	CTCF	chr8:10332200-10332350	HFF	foreskin:	n/a	n/a
24	CTCF	chr8:10331850-10332193	H1-hESC	embryonic stem cell:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
25	CTCF	chr8:10331904-10332192	K562	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
26	CTCF	chr8:10331992-10332084	Fibrobl	skin:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
27	CTCF	chr8:10331965-10332142	HepG2	liver:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
28	CTCF	chr8:10331980-10332130	K562	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
29	CTCF	chr8:10331960-10332110	HRPEpiC	eye:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
30	CTCF	chr8:10332020-10332170	HFF	foreskin:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
31	CTCF	chr8:10331934-10332181	MCF-7	breast:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
32	CTCF	chr8:10331941-10332186	HepG2	liver:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
33	CTCF	chr8:10331920-10332070	NHDF-neo	bronchial:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
34	CTCF	chr8:10332000-10332150	HUVEC	blood vessel:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
35	CTCF	chr8:10331980-10332130	GM12873	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
36	CTCF	chr8:10332120-10332270	GM12870	blood:	n/a	n/a
37	CTCF	chr8:10331862-10332158	H1-hESC	embryonic stem cell:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
38	CTCF	chr8:10331900-10332050	NHEK	skin:	n/a	n/a
39	CTCF	chr8:10331972-10332147	ProgFib	skin:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
40	CTCF	chr8:10331980-10332130	Caco-2	colon:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
41	CTCF	chr8:10331958-10332132	NHEK	skin:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
42	CTCF	chr8:10332000-10332150	GM12873	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
43	CTCF	chr8:10331900-10332050	SAEC	small airway:	n/a	n/a
44	CTCF	chr8:10331954-10332146	LNCaP	prostate:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
45	CTCF	chr8:10330660-10330810	HepG2	liver:	n/a	n/a
46	CTCF	chr8:10331980-10332130	BE2_C	brain:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
47	CTCF	chr8:10332080-10332230	WI-38	lung:	n/a	n/a
48	CTCF	chr8:10331940-10332090	Caco-2	colon:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
49	CTCF	chr8:10332004-10332128	GM12878	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054
50	CTCF	chr8:10332005-10332117	GM12878	blood:	n/a	chr8:10332039-10332057 chr8:10332045-10332054 chr8:10332040-10332056 chr8:10332042-10332052 chr8:10332041-10332054

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:10281970..10284229-chr8:10318464..10320467,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS55-1	chr8:10332075-10332141	ENSG00000253641
2	lnc-MSRA-3	chr8:10328326-10328856	NONHSAT124989

Variant related genes	Relation type
RNU6-729P	TF binding region
ENSG00000253641	TF binding region

Extended variants
information (count: 1080 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1986358	chr8:10316170-10316171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147862720	chr8:10316179-10316180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189393876	chr8:10316211-10316212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs1986357	chr8:10316236-10316237	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs112442352	chr8:10316237-10316238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111387392	chr8:10316238-10316239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532777869	chr8:10316297-10316298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141502062	chr8:10316335-10316336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147040253	chr8:10316340-10316341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs80217914	chr8:10316361-10316362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34851527	chr8:10316391-10316392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4841348	chr8:10316403-10316404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs138193708	chr8:10316414-10316415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56410018	chr8:10316416-10316417	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs554287129	chr8:10316432-10316433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566108958	chr8:10316451-10316452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368005506	chr8:10316455-10316456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538420356	chr8:10316502-10316503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577282915	chr8:10316521-10316522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545849743	chr8:10316527-10316528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556523335	chr8:10316546-10316547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576216281	chr8:10316560-10316561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541710018	chr8:10316562-10316563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561692286	chr8:10316569-10316570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12546919	chr8:10316570-10316571	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs540858829	chr8:10316587-10316588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78358277	chr8:10316603-10316604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75108294	chr8:10316616-10316617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549465711	chr8:10316623-10316624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149158687	chr8:10316651-10316652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569645265	chr8:10316675-10316676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs56359131	chr8:10316688-10316689	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs548896930	chr8:10316697-10316698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568798955	chr8:10316700-10316701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74374016	chr8:10316707-10316708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62490583	chr8:10316754-10316755	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570810746	chr8:10316759-10316760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184505021	chr8:10316760-10316761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557283126	chr8:10316783-10316784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs56184206	chr8:10316794-10316795	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs188214718	chr8:10316795-10316796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535102770	chr8:10316847-10316848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576379991	chr8:10316869-10316870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535481970	chr8:10316881-10316882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200996144	chr8:10316884-10316885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs397796177	chr8:10316885-10316886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555224788	chr8:10316886-10316887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531428702	chr8:10316899-10316900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540803288	chr8:10316908-10316909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564310217	chr8:10316931-10316932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Epilepsy	20502679	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Osteosarcoma	21215367	CNVD
Gastric cancer	21811585	CNVD

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10292200-10321400	Weak transcription	Fetal Brain Male	brain
2	chr8:10304400-10328200	Weak transcription	Fetal Brain Female	brain
3	chr8:10310800-10321000	Weak transcription	Pancreas	Pancrea
4	chr8:10313000-10317400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr8:10315400-10318200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:10315400-10328400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:10315600-10321000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:10319200-10330600	Weak transcription	Gastric	stomach
9	chr8:10319600-10319800	ZNF genes & repeats	Brain Germinal Matrix	brain
10	chr8:10319800-10329400	Weak transcription	Brain Germinal Matrix	brain
11	chr8:10321000-10321200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:10321000-10321400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr8:10321400-10321600	Enhancers	Fetal Brain Male	brain
14	chr8:10322000-10335400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr8:10324000-10324400	Weak transcription	Liver	Liver
16	chr8:10324400-10324600	ZNF genes & repeats	Aorta	Aorta
17	chr8:10324600-10325600	Weak transcription	Aorta	Aorta
18	chr8:10324800-10325600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:10325000-10325200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:10325200-10330600	Weak transcription	Liver	Liver
21	chr8:10326000-10326200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:10326200-10336800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:10327000-10328200	Weak transcription	Aorta	Aorta
24	chr8:10327000-10336600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr8:10328200-10328400	ZNF genes & repeats	Aorta	Aorta
26	chr8:10328200-10328600	ZNF genes & repeats	Ovary	ovary
27	chr8:10328200-10331200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr8:10328200-10331600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
29	chr8:10328200-10335200	Weak transcription	Brain Substantia Nigra	brain
30	chr8:10328200-10338000	Strong transcription	Fetal Brain Female	brain
31	chr8:10328400-10328600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
32	chr8:10328400-10330000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
33	chr8:10328600-10330600	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr8:10328600-10330600	Weak transcription	Ovary	ovary
35	chr8:10329000-10330600	Weak transcription	Brain Anterior Caudate	brain
36	chr8:10329000-10345600	Weak transcription	Brain Hippocampus Middle	brain
37	chr8:10329200-10329600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr8:10329200-10331800	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr8:10329200-10339200	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr8:10329200-10340400	Weak transcription	Brain Angular Gyrus	brain
41	chr8:10329200-10342200	Weak transcription	Brain Cingulate Gyrus	brain
42	chr8:10329400-10329800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:10329400-10329800	ZNF genes & repeats	Brain Germinal Matrix	brain
44	chr8:10329600-10329800	ZNF genes & repeats	Left Ventricle	heart
45	chr8:10329800-10332800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr8:10329800-10337200	Weak transcription	Left Ventricle	heart
47	chr8:10330000-10337000	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr8:10330200-10335000	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr8:10330200-10338000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr8:10330600-10330800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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