Variant report

Variant	nsv1037830
Chromosome Location	chr11:100802521-100818129
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	chr11:100803313-100803463	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:100803246-100803827	K562	blood:	n/a	n/a
3	ATF1	chr11:100803319-100803533	K562	blood:	n/a	n/a
4	CTCF	chr11:100803280-100803430	HBMEC	blood vessel:	n/a	chr11:100803414-100803430 chr11:100803408-100803429
5	CTCF	chr11:100803340-100803490	GM12864	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
6	CTCF	chr11:100803380-100803530	HA-sp	spinal cord:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
7	CTCF	chr11:100803360-100803510	AoAF	blood vessel:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
8	CTCF	chr11:100803369-100803495	HepG2	liver:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
9	CTCF	chr11:100803340-100803490	HUVEC	blood vessel:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
10	CTCF	chr11:100803300-100803450	HFF	foreskin:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
11	CTCF	chr11:100803060-100803726	A549	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
12	CTCF	chr11:100803380-100803530	MCF-7	breast:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
13	CTCF	chr11:100803400-100803550	GM12874	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
14	CTCF	chr11:100803400-100803550	HAc	cerebellar:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
15	CTCF	chr11:100803285-100803593	A549	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
16	CTCF	chr11:100803340-100803490	HCPEpiC	choroid plexus:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
17	CTCF	chr11:100803360-100803510	GM12878	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
18	CTCF	chr11:100803257-100803663	T-47D	breast:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
19	CTCF	chr11:100803215-100803666	IMR90	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
20	CTCF	chr11:100803320-100803470	HMF	breast:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
21	CTCF	chr11:100803238-100803566	Medullo	brain:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
22	CTCF	chr11:100803300-100803450	GM12873	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
23	CTCF	chr11:100803280-100803430	NHDF-neo	bronchial:	n/a	chr11:100803414-100803430 chr11:100803408-100803429
24	CTCF	chr11:100803320-100803470	HFF-Myc	foreskin:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
25	CTCF	chr11:100803328-100803531	K562	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
26	CTCF	chr11:100803400-100803550	K562	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
27	CTCF	chr11:100803360-100803510	HRE	kidney:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
28	CTCF	chr11:100803227-100803630	K562	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
29	CTCF	chr11:100803300-100803450	GM12866	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
30	CTCF	chr11:100803380-100803530	BE2_C	brain:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
31	CTCF	chr11:100803340-100803490	AG04450	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
32	CTCF	chr11:100803358-100803501	GM10266	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
33	CTCF	chr11:100803340-100803490	GM12875	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
34	CTCF	chr11:100803320-100803470	HPAF	blood vessel:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
35	CTCF	chr11:100803300-100803522	HepG2	liver:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
36	CTCF	chr11:100803239-100803510	ECC-1	luminal epithelium:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
37	CTCF	chr11:100803400-100803550	HBMEC	blood vessel:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
38	CTCF	chr11:100803300-100803450	AG04450	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
39	CTCF	chr11:100803244-100803515	A549	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
40	CTCF	chr11:100803380-100803530	GM06990	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
41	CTCF	chr11:100803340-100803490	AG09309	skin:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
42	CTCF	chr11:100803360-100803510	HPF	lung:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
43	CTCF	chr11:100803460-100803610	BE2_C	brain:	n/a	n/a
44	CTCF	chr11:100803320-100803470	HL-60	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
45	CTCF	chr11:100803360-100803510	HRPEpiC	eye:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
46	CTCF	chr11:100803327-100803512	GM13977	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
47	CTCF	chr11:100803361-100803455	GM13976	blood:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
48	CTCF	chr11:100803340-100803490	AG04449	skin:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429
49	CTCF	chr11:100803280-100803430	GM12865	blood:	n/a	chr11:100803414-100803430 chr11:100803408-100803429
50	CTCF	chr11:100803340-100803490	HMEC	breast:	n/a	chr11:100803413-100803431 chr11:100803414-100803430 chr11:100803408-100803429

No.	Distal block	Cell Line	Cell type
1	chr11:100805825..100807914-chr11:100811015..100813625,3	K562	blood:
2	chr11:100448550..100449412-chr11:100802794..100803475,2	K562	blood:
3	chr11:100804677..100807914-chr11:100810511..100812906,3	K562	blood:
4	chr11:100447225..100447948-chr11:100803021..100803878,2	MCF-7	breast:
5	chr11:100601693..100603676-chr11:100800928..100802869,2	MCF-7	breast:
6	chr11:100805825..100807914-chr11:100811015..100813625,3	K562	blood:
7	chr11:100446930..100447515-chr11:100802994..100803615,2	MCF-7	breast:
8	chr11:100446552..100447865-chr11:100802950..100803911,5	K562	blood:
9	chr11:100802948..100803667-chr11:101307051..101307600,2	K562	blood:
10	chr11:100817953..100820202-chr11:100996592..100999547,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000238388	TF binding region
ENSG00000238388	chromatin interactions

Extended variants
information (count: 664 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10791432	chr11:100802521-100802522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552128502	chr11:100802527-100802528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189569029	chr11:100802532-100802533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144889992	chr11:100802554-100802555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147958993	chr11:100802592-100802593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192254012	chr11:100802646-100802647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543277732	chr11:100802673-100802674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs653344	chr11:100802712-100802713	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs528665452	chr11:100802714-100802715	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs182363493	chr11:100802722-100802723	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552063613	chr11:100802770-100802771	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs565396451	chr11:100802785-100802786	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs530934813	chr11:100802831-100802832	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs534421981	chr11:100802855-100802856	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs148968242	chr11:100802867-100802868	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs536334234	chr11:100802896-100802897	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377404232	chr11:100802904-100802905	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs548796584	chr11:100802911-100802912	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs567405927	chr11:100802954-100802955	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs116735345	chr11:100802995-100802996	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs2186784	chr11:100803010-100803011	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs558043345	chr11:100803026-100803027	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs184304627	chr11:100803042-100803043	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs73580117	chr11:100803043-100803044	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs556977430	chr11:100803142-100803143	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs573806286	chr11:100803170-100803171	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs542765831	chr11:100803218-100803219	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs559456460	chr11:100803227-100803228	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs640326	chr11:100803267-100803268	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs189664927	chr11:100803279-100803280	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs565620509	chr11:100803283-100803284	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs531103992	chr11:100803286-100803287	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs6590825	chr11:100803293-100803294	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs368456746	chr11:100803295-100803296	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs12273212	chr11:100803304-100803305	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs530012106	chr11:100803483-100803484	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs17095820	chr11:100803590-100803591	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs566587723	chr11:100803632-100803633	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs534822134	chr11:100803645-100803646	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs143760798	chr11:100803656-100803657	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs571549493	chr11:100803660-100803661	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs11224521	chr11:100803717-100803718	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs558991300	chr11:100803780-100803781	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs181035022	chr11:100803781-100803782	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs112927258	chr11:100803872-100803873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375060905	chr11:100803877-100803878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573250547	chr11:100803934-100803935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557261474	chr11:100803958-100803959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79213484	chr11:100803982-100803983	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs536213558	chr11:100804061-100804062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal cancer	21851588	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:100772000-100831400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr11:100773800-100809800	Weak transcription	Left Ventricle	heart
3	chr11:100774800-100812800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr11:100784000-100808800	Weak transcription	Primary B cells from cord blood	blood
5	chr11:100785400-100838400	Weak transcription	Fetal Intestine Small	intestine
6	chr11:100786800-100806800	Weak transcription	Placenta	Placenta
7	chr11:100790000-100803200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr11:100790200-100812600	Weak transcription	Stomach Mucosa	stomach
9	chr11:100790400-100806600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr11:100793400-100807000	Weak transcription	Liver	Liver
11	chr11:100794200-100803000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr11:100794200-100807000	Weak transcription	Fetal Muscle Leg	muscle
13	chr11:100794400-100812800	Weak transcription	Fetal Stomach	stomach
14	chr11:100795600-100807400	Weak transcription	Fetal Muscle Trunk	muscle
15	chr11:100797600-100811800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:100798600-100807600	Weak transcription	Ovary	ovary
17	chr11:100798600-100811600	Weak transcription	Fetal Lung	lung
18	chr11:100798600-100812800	Weak transcription	Brain Hippocampus Middle	brain
19	chr11:100798600-100826600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr11:100798600-100828200	Weak transcription	Gastric	stomach
21	chr11:100798800-100807000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr11:100798800-100811400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr11:100798800-100832200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr11:100799200-100804600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:100799200-100812800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:100799200-100812800	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr11:100800200-100846600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr11:100800800-100835800	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr11:100801000-100802800	Weak transcription	GM12878-XiMat	blood
30	chr11:100801000-100807000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr11:100801000-100809600	Weak transcription	Osteobl	bone
32	chr11:100801000-100812000	Weak transcription	Fetal Heart	heart
33	chr11:100801000-100814800	Weak transcription	HSMM	muscle
34	chr11:100801000-100819600	Weak transcription	HSMMtube	muscle
35	chr11:100801000-100823200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr11:100801000-100832400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr11:100801000-100835000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr11:100801200-100802800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr11:100801400-100812600	Weak transcription	A549	lung
40	chr11:100801400-100833800	Weak transcription	NH-A	brain
41	chr11:100802800-100803000	Enhancers	Primary B cells from peripheral blood	blood
42	chr11:100802800-100803000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr11:100802800-100803600	Enhancers	GM12878-XiMat	blood
44	chr11:100802800-100803600	Enhancers	K562	blood
45	chr11:100803000-100803400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr11:100803000-100804000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr11:100803000-100822600	Weak transcription	Primary B cells from peripheral blood	blood
48	chr11:100803200-100803600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr11:100803400-100803600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr11:100803600-100806400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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