Variant report

Variant	nsv1026034
Chromosome Location	chr8:1561756-1596773
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	BATF	chr8:1583024-1583221	GM12878	blood:	n/a	chr8:1583128-1583139
2	BHLHE40	chr8:1563001-1563164	K562	blood:	n/a	n/a
3	BHLHE40	chr8:1589261-1589514	K562	blood:	n/a	chr8:1589361-1589370 chr8:1589362-1589371 chr8:1589355-1589376 chr8:1589361-1589370
4	CEBPB	chr8:1577269-1577487	HepG2	liver:	n/a	chr8:1577393-1577404 chr8:1577393-1577406 chr8:1577395-1577406 chr8:1577393-1577406 chr8:1577395-1577404
5	CEBPB	chr8:1580676-1580906	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:1580668-1580977	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr8:1591266-1591306	MCF-7	breast:	n/a	n/a
8	CTCF	chr8:1574369-1574425	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr8:1571043-1571139	H1-hESC	embryonic stem cell:	n/a	chr8:1571110-1571123
10	CTCF	chr8:1595864-1595915	MCF-7	breast:	n/a	n/a
11	CTCF	chr8:1595860-1596010	A549	lung:	n/a	n/a
12	CTCF	chr8:1564045-1564082	GM13977	blood:	n/a	n/a
13	CTCF	chr8:1591277-1591285	MCF-7	breast:	n/a	n/a
14	CTCF	chr8:1574798-1574892	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:1595780-1595930	HepG2	liver:	n/a	n/a
16	CTCF	chr8:1590436-1590447	MCF-7	breast:	n/a	n/a
17	CTCF	chr8:1571562-1571637	Fibrobl	skin:	n/a	n/a
18	CTCF	chr8:1574740-1574920	K562	blood:	n/a	n/a
19	ELK1	chr8:1582547-1582567	Hela-S3	cervix:	n/a	n/a
20	ELK1	chr8:1589785-1589810	K562	blood:	n/a	n/a
21	EP300	chr8:1577960-1577963	GM12878	blood:	n/a	n/a
22	ESR1	chr8:1571462-1571868	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
23	ESR1	chr8:1571384-1572033	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
24	ESR1	chr8:1571311-1571914	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
25	ESR1	chr8:1571268-1572042	ECC-1	luminal epithelium:	n/a	chr8:1571644-1571659 chr8:1571665-1571680 chr8:1571602-1571617
26	FOXA1	chr8:1579862-1580193	HepG2	liver:	n/a	chr8:1580014-1580029
27	FOXA1	chr8:1579869-1580116	HepG2	liver:	n/a	chr8:1580014-1580029
28	FOXA1	chr8:1579905-1580112	HepG2	liver:	n/a	chr8:1580014-1580029
29	FOXA1	chr8:1579880-1580100	T-47D	breast:	n/a	chr8:1580014-1580029
30	FOXA1	chr8:1581553-1581686	T-47D	breast:	n/a	n/a
31	FOXA1	chr8:1579783-1580115	HepG2	liver:	n/a	chr8:1580014-1580029
32	FOXA2	chr8:1579857-1580107	HepG2	liver:	n/a	n/a
33	GATA2	chr8:1566862-1567163	SH-SY5Y	brain:	n/a	n/a
34	IRF1	chr8:1570228-1570235	K562	blood:	n/a	n/a
35	JUND	chr8:1581537-1581603	H1-hESC	embryonic stem cell:	n/a	n/a
36	KAP1	chr8:1581108-1582241	HEK293	kidney:	n/a	chr8:1581849-1581857
37	KAP1	chr8:1581265-1582253	U2OS	brain:	n/a	chr8:1581849-1581857
38	MAFF	chr8:1571227-1571455	K562	blood:	n/a	n/a
39	MAFF	chr8:1573527-1573890	HepG2	liver:	n/a	chr8:1573697-1573715
40	MAFF	chr8:1573543-1573870	K562	blood:	n/a	chr8:1573697-1573715
41	MAFK	chr8:1573557-1573842	Hela-S3	cervix:	n/a	chr8:1573699-1573710 chr8:1573699-1573715 chr8:1573698-1573712 chr8:1573699-1573714 chr8:1573699-1573710
42	MAFK	chr8:1571327-1571371	K562	blood:	n/a	chr8:1571348-1571358 chr8:1571349-1571358
43	MAFK	chr8:1573539-1573885	HepG2	liver:	n/a	chr8:1573699-1573710 chr8:1573699-1573715 chr8:1573698-1573712 chr8:1573699-1573714 chr8:1573699-1573710
44	MAFK	chr8:1573563-1573852	H1-hESC	embryonic stem cell:	n/a	chr8:1573699-1573710 chr8:1573699-1573715 chr8:1573698-1573712 chr8:1573699-1573714 chr8:1573699-1573710
45	MAFK	chr8:1573534-1573888	IMR90	lung:	n/a	chr8:1573699-1573710 chr8:1573699-1573715 chr8:1573698-1573712 chr8:1573699-1573714 chr8:1573699-1573710
46	MAFK	chr8:1573524-1573889	HepG2	liver:	n/a	chr8:1573699-1573710 chr8:1573699-1573715 chr8:1573698-1573712 chr8:1573699-1573714 chr8:1573699-1573710
47	MAFK	chr8:1573547-1573873	K562	blood:	n/a	chr8:1573699-1573710 chr8:1573699-1573715 chr8:1573698-1573712 chr8:1573699-1573714 chr8:1573699-1573710
48	MAX	chr8:1589296-1589441	K562	blood:	n/a	chr8:1589356-1589375 chr8:1589359-1589372
49	MAX	chr8:1562945-1563066	NB4	blood:	n/a	n/a
50	MYC	chr8:1571727-1571802	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1592281-1592331	LNCaP	prostate:	n/a
2	chr8:1592451-1592501	SK-N-SH	brain:	n/a
3	chr8:1592281-1592331	AG04450	lung:	fetal
4	chr8:1575750-1575800	GM06990	blood:	n/a
5	chr8:1592281-1592331	LNCaP	prostate:	n/a
6	chr8:1592451-1592501	SK-N-SH	brain:	n/a
7	chr8:1592281-1592331	AG04450	lung:	fetal
8	chr8:1575750-1575800	GM06990	blood:	n/a
9	chr8:1590039-1590089	HMEC	breast:	n/a
10	chr8:1570956-1571006	HEEpiC	esophagus:	n/a
11	chr8:1585876-1585926	SKMC	muscle:	n/a
12	chr8:1588899-1588949	SK-N-SH_RA	brain:	n/a
13	chr8:1592736-1592786	HCF	heart:	n/a
14	chr8:1581122-1581172	U87	brain:	n/a
15	chr8:1581568-1581618	HRE	kidney:	n/a
16	chr8:1588359-1588409	GM12892	blood:	n/a
17	chr8:1563040-1563090	MCF10A-Er-Src	breast:	n/a
18	chr8:1581598-1581648	NB4	blood:	n/a
19	chr8:1588899-1588949	GM12891	blood:	n/a
20	chr8:1585929-1585979	ovcar-3	ovarian:	n/a
21	chr8:1589165-1589215	GM12891	blood:	n/a
22	chr8:1575750-1575800	HepG2	liver:	n/a
23	chr8:1588403-1588453	Jurkat	blood:	n/a
24	chr8:1589165-1589215	HEEpiC	esophagus:	n/a
25	chr8:1570956-1571006	SK-N-SH	brain:	n/a
26	chr8:1588618-1588668	BE2_C	brain:	n/a
27	chr8:1570715-1570765	PANC-1	pancreas:	n/a
28	chr8:1571105-1571155	SK-N-MC	brain:	n/a
29	chr8:1579108-1579158	AG09309	skin:	n/a
30	chr8:1590039-1590089	U87	brain:	n/a
31	chr8:1588359-1588409	GM06990	blood:	n/a
32	chr8:1588359-1588409	T-47D	breast:	n/a
33	chr8:1579240-1579290	HIPEpiC	eye:	n/a
34	chr8:1588822-1588872	AoSMC	blood vessel:	n/a
35	chr8:1579180-1579230	HCPEpiC	choroid plexus:	n/a
36	chr8:1585929-1585979	AoSMC	blood vessel:	n/a
37	chr8:1563040-1563090	ProgFib	skin:	n/a
38	chr8:1588403-1588453	HepG2	liver:	n/a
39	chr8:1592451-1592501	PANC-1	pancreas:	n/a
40	chr8:1579108-1579158	ovcar-3	ovarian:	n/a
41	chr8:1596244-1596294	AG04449	skin:	fetal
42	chr8:1592736-1592786	NHBE	bronchial:	n/a
43	chr8:1588618-1588668	MCF-7	breast:	n/a
44	chr8:1579240-1579290	ECC-1	luminal epithelium:	n/a
45	chr8:1581598-1581648	HL-60	blood:	n/a
46	chr8:1563113-1563163	HIPEpiC	eye:	n/a
47	chr8:1589165-1589215	SKMC	muscle:	n/a
48	chr8:1588359-1588409	HCM	heart:	n/a
49	chr8:1588403-1588453	AG09319	gingival:	n/a
50	chr8:1591382-1591432	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:154989909..154990782-chr8:1569714..1570480,2	MCF-7	breast:
2	chr8:1582447..1584354-chr8:1585808..1588032,2	K562	blood:
3	chr8:1578132..1580473-chr8:1601540..1604510,2	K562	blood:
4	chr8:1593850..1596302-chr8:1622198..1625044,2	K562	blood:
5	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
6	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
7	chr8:1582447..1584354-chr8:1585808..1588032,2	K562	blood:
8	chr8:1569188..1570751-chr8:1570808..1572953,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERICH1-6	chr8:1568540-1568679	ENSG00000253267.1
2	lnc-ERICH1-6	chr8:1567865-1568059	ENSG00000253267.1
3	lnc-ERICH1-6	chr8:1569302-1570583	ENSG00000253267.1

Variant related genes	Relation type
ENSG00000253267	TF binding region
ENSG00000253267	CpG island
ENSG00000253267	chromatin interactions
ENSG00000198010	chromatin interactions

Extended variants
information (count: 2434 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:2434 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7819115	chr8:1561756-1561757	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535922965	chr8:1561761-1561762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555873370	chr8:1561767-1561768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145295598	chr8:1561775-1561776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545441786	chr8:1561790-1561791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565233446	chr8:1561802-1561803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150599681	chr8:1561855-1561856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188153440	chr8:1561863-1561864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181355288	chr8:1561866-1561867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139548481	chr8:1561904-1561905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116837978	chr8:1561910-1561911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78997312	chr8:1561913-1561914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145233648	chr8:1561923-1561924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542348836	chr8:1561956-1561957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562237395	chr8:1561985-1561986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543988946	chr8:1561997-1561998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531452575	chr8:1562007-1562008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551509327	chr8:1562015-1562016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565045183	chr8:1562044-1562045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562313886	chr8:1562046-1562047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527544320	chr8:1562057-1562058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546697925	chr8:1562061-1562062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566897692	chr8:1562064-1562065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536107546	chr8:1562072-1562073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186317437	chr8:1562089-1562090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141307674	chr8:1562097-1562098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538442714	chr8:1562120-1562121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs118044042	chr8:1562121-1562122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551020999	chr8:1562145-1562146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559932018	chr8:1562158-1562159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191628590	chr8:1562177-1562178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527273664	chr8:1562179-1562180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554154843	chr8:1562183-1562184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112798569	chr8:1562188-1562189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35992977	chr8:1562229-1562230	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs542216232	chr8:1562236-1562237	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs562249271	chr8:1562241-1562242	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs549041283	chr8:1562246-1562247	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs143736692	chr8:1562253-1562254	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs182159696	chr8:1562267-1562268	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs186757150	chr8:1562275-1562276	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs191009794	chr8:1562276-1562277	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs369516862	chr8:1562290-1562291	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs117137731	chr8:1562357-1562358	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs183174930	chr8:1562390-1562391	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs549350672	chr8:1562397-1562398	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs146785317	chr8:1562421-1562422	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538301392	chr8:1562425-1562426	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551563223	chr8:1562426-1562427	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571845554	chr8:1562434-1562435	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	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
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	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
Breast cancer	21364760	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
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1553600-1562200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:1562200-1562600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:1562400-1562600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:1562400-1562600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:1562600-1564800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:1562600-1569400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:1562800-1572600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr8:1567800-1570200	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr8:1568000-1568400	Enhancers	Fetal Muscle Leg	muscle
10	chr8:1569400-1570000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:1569800-1570400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr8:1569800-1570400	Active TSS	Spleen	Spleen
13	chr8:1570000-1570400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr8:1570000-1571400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:1570200-1570800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:1570200-1571000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr8:1570400-1571600	Weak transcription	Spleen	Spleen
18	chr8:1570400-1579800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr8:1571400-1571800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:1571600-1571800	ZNF genes & repeats	Pancreas	Pancrea
21	chr8:1571600-1571800	Enhancers	Spleen	Spleen
22	chr8:1571800-1574800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:1573200-1573400	Enhancers	Colon Smooth Muscle	Colon
24	chr8:1573400-1573800	Enhancers	Adipose Nuclei	Adipose
25	chr8:1573400-1573800	Flanking Active TSS	Colon Smooth Muscle	Colon
26	chr8:1573800-1574200	Enhancers	Colon Smooth Muscle	Colon
27	chr8:1574000-1574200	Enhancers	Fetal Muscle Leg	muscle
28	chr8:1574800-1575200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:1575000-1575200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr8:1575200-1575400	Enhancers	Spleen	Spleen
31	chr8:1575200-1599400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:1579800-1580000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr8:1579800-1581200	Enhancers	Fetal Brain Male	brain
34	chr8:1580000-1580800	Enhancers	Fetal Brain Female	brain
35	chr8:1580600-1581000	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr8:1580800-1581200	Active TSS	Gastric	stomach
37	chr8:1581400-1581800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr8:1593400-1594600	Weak transcription	Fetal Brain Male	brain
39	chr8:1594200-1594400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:1594400-1595000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:1595000-1595200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:1595800-1596800	Enhancers	Gastric	stomach
43	chr8:1596000-1596200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links