Variant report

Variant	nsv6347
Chromosome Location	chr8:110978143-111023190
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	BACH1	chr8:111011276-111011469	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr8:111010799-111010810	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:110996175-110996503	HepG2	liver:	n/a	chr8:110996318-110996329
4	CEBPB	chr8:110980027-110980297	A549	lung:	n/a	n/a
5	CTBP2	chr8:110985797-110987235	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTBP2	chr8:110987468-110988080	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr8:110987160-110987310	GM12872	blood:	n/a	n/a
8	CTCF	chr8:110986700-110986850	BJ	skin:	n/a	chr8:110986702-110986711
9	CTCF	chr8:110986383-110987016	MCF-7	breast:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
10	CTCF	chr8:110986700-110986850	BE2_C	brain:	n/a	chr8:110986702-110986711
11	CTCF	chr8:110986740-110986890	GM12878	blood:	n/a	n/a
12	CTCF	chr8:110986800-110986950	GM06990	blood:	n/a	n/a
13	CTCF	chr8:110987000-110987150	RPTEC	kidney:	n/a	n/a
14	CTCF	chr8:110986620-110986770	RPTEC	kidney:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
15	CTCF	chr8:110986720-110986870	GM12869	blood:	n/a	n/a
16	CTCF	chr8:110986627-110987021	GM19239	blood:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
17	CTCF	chr8:110987020-110987170	HAc	cerebellar:	n/a	n/a
18	CTCF	chr8:110986700-110986850	GM12865	blood:	n/a	chr8:110986702-110986711
19	CTCF	chr8:110986482-110986498	ProgFib	skin:	n/a	n/a
20	CTCF	chr8:110986700-110986850	GM12878	blood:	n/a	chr8:110986702-110986711
21	CTCF	chr8:110986315-110987186	MCF-7	breast:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
22	CTCF	chr8:110986780-110986930	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr8:110986410-110987128	MCF-7	breast:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
24	CTCF	chr8:110987026-110987149	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:110986622-110986624	GM19239	blood:	n/a	n/a
26	CTCF	chr8:110986553-110986978	MCF-7	breast:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
27	CTCF	chr8:110987051-110987097	GM19238	blood:	n/a	n/a
28	CTCF	chr8:110986503-110986530	ProgFib	skin:	n/a	n/a
29	CTCF	chr8:110986673-110986927	GM12891	blood:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
30	CTCF	chr8:110986713-110986895	GM13977	blood:	n/a	n/a
31	CTCF	chr8:110986740-110986890	AG10803	skin:	n/a	n/a
32	CTCF	chr8:110986735-110986883	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr8:110986640-110986790	RPTEC	kidney:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
34	CTCF	chr8:110986946-110986947	NHEK	skin:	n/a	n/a
35	CTCF	chr8:110986720-110986870	GM12868	blood:	n/a	n/a
36	CTCF	chr8:110994560-110994590	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:110986680-110986830	HEEpiC	esophagus:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
38	CTCF	chr8:110986755-110986891	GM20000	blood:	n/a	n/a
39	CTCF	chr8:110986720-110986870	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:110986604-110986850	A549	lung:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
41	CTCF	chr8:110986740-110986890	GM12867	blood:	n/a	n/a
42	CTCF	chr8:110986720-110986870	HRE	kidney:	n/a	n/a
43	CTCF	chr8:110986760-110986910	GM12865	blood:	n/a	n/a
44	CTCF	chr8:110986680-110986830	AG09309	skin:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
45	CTCF	chr8:110986740-110986890	A549	lung:	n/a	n/a
46	CTCF	chr8:110986720-110986870	GM12872	blood:	n/a	n/a
47	CTCF	chr8:110986640-110986790	GM12870	blood:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
48	CTCF	chr8:110986600-110986750	HMEC	breast:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
49	CTCF	chr8:110986416-110987014	MCF-7	breast:	n/a	chr8:110986699-110986709 chr8:110986702-110986711
50	CTCF	chr8:110986680-110986830	NHEK	skin:	n/a	chr8:110986699-110986709 chr8:110986702-110986711

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110986974-110987024	SK-N-SH_RA	brain:	n/a
2	chr8:110986685-110986735	HepG2	liver:	n/a
3	chr8:110986982-110987032	SKMC	muscle:	n/a
4	chr8:110986870-110986920	ovcar-3	ovarian:	n/a
5	chr8:110987019-110987069	PrEC	prostate:	n/a
6	chr8:110986870-110986920	HEEpiC	esophagus:	n/a
7	chr8:110988256-110988306	HAEpiC	amniotic membrane:	n/a
8	chr8:110987530-110987580	GM12878	blood:	n/a
9	chr8:110990365-110990415	GM06990	blood:	n/a
10	chr8:110990365-110990415	T-47D	breast:	n/a
11	chr8:110982709-110982759	HL-60	blood:	n/a
12	chr8:110988256-110988306	HNPCEpiC	eye:	n/a
13	chr8:110988256-110988306	HRPEpiC	eye:	n/a
14	chr8:110984715-110984765	NH-A	brain:	n/a
15	chr8:110986371-110986421	GM19239	blood:	n/a
16	chr8:110988071-110988121	SKMC	muscle:	n/a
17	chr8:110988248-110988298	AG09319	gingival:	n/a
18	chr8:110986982-110987032	HNPCEpiC	eye:	n/a
19	chr8:110984575-110984625	HEEpiC	esophagus:	n/a
20	chr8:110986982-110987032	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:110986870-110986920	A549	lung:	n/a
22	chr8:110990365-110990415	SK-N-SH	brain:	n/a
23	chr8:110982709-110982759	Hepatocyte	liver:	n/a
24	chr8:110986974-110987024	H1-hESC	embryonic stem cell:	embryo
25	chr8:110986974-110987024	HIPEpiC	eye:	n/a
26	chr8:110986982-110987032	MCF-7	breast:	n/a
27	chr8:110986870-110986920	HL-60	blood:	n/a
28	chr8:110988071-110988121	K562	blood:	n/a
29	chr8:110988256-110988306	SAEC	small airway:	n/a
30	chr8:110988256-110988306	PANC-1	pancreas:	n/a
31	chr8:110990365-110990415	NHBE	bronchial:	n/a
32	chr8:110987530-110987580	ProgFib	skin:	n/a
33	chr8:110987019-110987069	HCF	heart:	n/a
34	chr8:110982709-110982759	HEEpiC	esophagus:	n/a
35	chr8:110986974-110987024	HCT-116	colon:	n/a
36	chr8:110988043-110988093	SK-N-SH	brain:	n/a
37	chr8:110989116-110989166	A549	lung:	n/a
38	chr8:110986685-110986735	RPTEC	kidney:	n/a
39	chr8:110986870-110986920	LNCaP	prostate:	n/a
40	chr8:110988256-110988306	HIPEpiC	eye:	n/a
41	chr8:110982709-110982759	AG04449	skin:	fetal
42	chr8:110986974-110987024	NHDF-neo	bronchial:	n/a
43	chr8:110989116-110989166	ProgFib	skin:	n/a
44	chr8:110988444-110988494	NHDF-neo	bronchial:	n/a
45	chr8:110987019-110987069	HCPEpiC	choroid plexus:	n/a
46	chr8:110988444-110988494	HL-60	blood:	n/a
47	chr8:110988071-110988121	HUVEC	blood vessel:	n/a
48	chr8:110987530-110987580	HEEpiC	esophagus:	n/a
49	chr8:110987946-110987996	SAEC	small airway:	n/a
50	chr8:110988248-110988298	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:111011938..111014551-chr8:111015885..111018861,2	MCF-7	breast:
2	chr8:110981502..110984077-chr8:110985344..110987885,2	MCF-7	breast:
3	chr8:111003607..111005955-chr8:111007039..111008602,2	MCF-7	breast:
4	chr8:111011938..111014551-chr8:111015885..111018861,2	MCF-7	breast:
5	chr8:111003607..111005955-chr8:111007039..111008602,2	MCF-7	breast:
6	chr8:110345039..110348121-chr8:110985396..110989742,4	MCF-7	breast:
7	chr8:110986569..110989011-chr8:110990714..110992570,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-1	chr8:110986541-110987010	ENSG00000255402.1
2	lnc-RP11-422N16.3.1-1	chr8:110986172-110986254	ENSG00000255402.1

Variant related genes	Relation type
ENSG00000255402	TF binding region
KCNV1	TF binding region
ENSG00000255402	CpG island
KCNV1	CpG island
ENSG00000120533	chromatin interactions
ENSG00000255402	chromatin interactions
ENSG00000120526	chromatin interactions
ENSG00000164794	chromatin interactions

Extended variants
information (count: 1106 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1106 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114834663	chr8:110978213-110978214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145755650	chr8:110978295-110978296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530321694	chr8:110978328-110978329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546937464	chr8:110978409-110978410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557897817	chr8:110978421-110978422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192187237	chr8:110978423-110978424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538897026	chr8:110978596-110978597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141947220	chr8:110978605-110978606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552038615	chr8:110978629-110978630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569255061	chr8:110978648-110978649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373765894	chr8:110978650-110978651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570769066	chr8:110978673-110978674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554991644	chr8:110978692-110978693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574932463	chr8:110978718-110978719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536526744	chr8:110978767-110978768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553334833	chr8:110978855-110978856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572961806	chr8:110978917-110978918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544899436	chr8:110978951-110978952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564949307	chr8:110978970-110978971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540255393	chr8:110978978-110978979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575255119	chr8:110979013-110979014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543944268	chr8:110979021-110979022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560549556	chr8:110979042-110979043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529669398	chr8:110979043-110979044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs56294323	chr8:110979084-110979085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528382815	chr8:110979090-110979091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546874298	chr8:110979099-110979100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557043726	chr8:110979127-110979128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532692447	chr8:110979129-110979130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184030109	chr8:110979156-110979157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560221812	chr8:110979162-110979163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569473900	chr8:110979176-110979177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538336625	chr8:110979243-110979244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548726939	chr8:110979266-110979267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568446131	chr8:110979420-110979421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534197441	chr8:110979424-110979425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577182451	chr8:110979480-110979481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148937775	chr8:110979483-110979484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553277776	chr8:110979517-110979518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573061190	chr8:110979565-110979566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573840336	chr8:110979592-110979593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187821437	chr8:110979604-110979605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562537644	chr8:110979611-110979612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142773024	chr8:110979707-110979708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114699150	chr8:110979811-110979812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192504225	chr8:110979831-110979832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140376524	chr8:110979836-110979837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17468375	chr8:110979845-110979846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs550618282	chr8:110979855-110979856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs17468410	chr8:110979871-110979872	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:95)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	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
Cancer	20164919	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	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
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
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	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
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110977800-110986000	Weak transcription	Spleen	Spleen
2	chr8:110978000-110978600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:110978000-110984400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr8:110978600-110981200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:110979000-110979200	Enhancers	Fetal Brain Male	brain
6	chr8:110979200-110983800	Weak transcription	Fetal Brain Male	brain
7	chr8:110980200-110980800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr8:110980800-110981000	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr8:110981000-110983200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr8:110981200-110981400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:110983400-110983800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
12	chr8:110983600-110986000	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr8:110983600-110986800	Active TSS	Fetal Brain Female	brain
14	chr8:110983800-110984200	Enhancers	Fetal Brain Male	brain
15	chr8:110984000-110986000	Weak transcription	Colonic Mucosa	Colon
16	chr8:110984200-110984400	Flanking Active TSS	Fetal Brain Male	brain
17	chr8:110984200-110985800	Active TSS	Brain Angular Gyrus	brain
18	chr8:110984400-110984600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:110984400-110984800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr8:110984400-110985000	Enhancers	Fetal Brain Male	brain
21	chr8:110984400-110985000	Strong transcription	Rectal Mucosa Donor 29	rectum
22	chr8:110984600-110984800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr8:110984600-110984800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr8:110984800-110986200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:110985000-110986000	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr8:110985200-110986000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
27	chr8:110985600-110985800	Weak transcription	Pancreas	Pancrea
28	chr8:110985600-110986200	Enhancers	Fetal Heart	heart
29	chr8:110985600-110986800	Active TSS	Brain Anterior Caudate	brain
30	chr8:110985800-110986000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:110985800-110986000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr8:110985800-110986000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:110985800-110986000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
34	chr8:110985800-110986000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
35	chr8:110985800-110986000	Active TSS	Fetal Brain Male	brain
36	chr8:110985800-110986000	Enhancers	Pancreas	Pancrea
37	chr8:110985800-110986000	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr8:110985800-110986200	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr8:110985800-110987400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
40	chr8:110986000-110986200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
41	chr8:110986000-110986200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:110986000-110986200	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:110986000-110986200	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:110986000-110986200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr8:110986000-110986200	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr8:110986000-110986200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:110986000-110986200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
48	chr8:110986000-110986200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
49	chr8:110986000-110986200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr8:110986000-110986200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links