Variant report

Variant	esv3348305
Chromosome Location	chr11:67764314-67764715
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	chr11:67764516-67764536	K562	blood:	n/a	n/a
2	ATF2	chr11:67764062-67764385	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr11:67764134-67764475	K562	blood:	n/a	n/a
4	ATF3	chr11:67764283-67764396	GM12878	blood:	n/a	n/a
5	BACH1	chr11:67763868-67764564	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr11:67764009-67764693	A549	lung:	n/a	n/a
7	BCL3	chr11:67764221-67765106	A549	lung:	n/a	n/a
8	BHLHE40	chr11:67763941-67764724	K562	blood:	n/a	n/a
9	CBX3	chr11:67763965-67764398	K562	blood:	n/a	n/a
10	CBX3	chr11:67763950-67764711	K562	blood:	n/a	n/a
11	CCNT2	chr11:67764125-67764664	K562	blood:	n/a	chr11:67764625-67764634 chr11:67764384-67764393
12	CEBPB	chr11:67764367-67764537	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr11:67764309-67764493	K562	blood:	n/a	n/a
14	CEBPB	chr11:67764220-67764583	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr11:67764200-67764766	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr11:67764425-67764548	K562	blood:	n/a	n/a
17	CREB1	chr11:67764340-67764567	A549	lung:	n/a	n/a
18	CTCF	chr11:67764068-67764321	K562	blood:	n/a	n/a
19	E2F6	chr11:67763799-67764724	H1-hESC	embryonic stem cell:	n/a	chr11:67764364-67764373
20	E2F6	chr11:67763908-67764365	K562	blood:	n/a	n/a
21	E2F6	chr11:67764015-67764686	K562	blood:	n/a	chr11:67764364-67764373
22	E2F6	chr11:67763973-67764726	K562	blood:	n/a	chr11:67764364-67764373
23	E2F6	chr11:67763948-67764550	H1-hESC	embryonic stem cell:	n/a	chr11:67764364-67764373
24	ELK1	chr11:67764491-67764571	K562	blood:	n/a	n/a
25	ELK1	chr11:67764397-67764591	Hela-S3	cervix:	n/a	n/a
26	EP300	chr11:67764339-67764491	K562	blood:	n/a	n/a
27	ETS1	chr11:67763982-67764508	K562	blood:	n/a	n/a
28	GTF2F1	chr11:67764506-67764515	H1-hESC	embryonic stem cell:	n/a	n/a
29	GTF2F1	chr11:67764144-67764317	K562	blood:	n/a	n/a
30	GTF2F1	chr11:67764691-67764861	Hela-S3	cervix:	n/a	n/a
31	HCFC1	chr11:67764252-67764532	K562	blood:	n/a	n/a
32	HMGN3	chr11:67764102-67764789	K562	blood:	n/a	n/a
33	IRF1	chr11:67764067-67764838	K562	blood:	n/a	chr11:67764360-67764374 chr11:67764602-67764616 chr11:67764313-67764327 chr11:67764435-67764449 chr11:67764380-67764394 chr11:67764760-67764774 chr11:67764621-67764635
34	JUND	chr11:67764155-67764645	K562	blood:	n/a	chr11:67764365-67764374
35	MAFK	chr11:67764462-67764862	Hela-S3	cervix:	n/a	n/a
36	MAX	chr11:67764086-67764511	K562	blood:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
37	MAX	chr11:67763974-67764616	K562	blood:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
38	MAX	chr11:67764271-67764462	NB4	blood:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
39	MAX	chr11:67764173-67764527	A549	lung:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
40	MAX	chr11:67764025-67764699	ECC-1	luminal epithelium:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
41	MAX	chr11:67763874-67765190	H1-hESC	embryonic stem cell:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
42	MAX	chr11:67763971-67764766	K562	blood:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
43	MAX	chr11:67763889-67765138	H1-hESC	embryonic stem cell:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
44	MAX	chr11:67764074-67764581	A549	lung:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
45	MAX	chr11:67763973-67764907	H1-hESC	embryonic stem cell:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
46	MAX	chr11:67764156-67764831	Hela-S3	cervix:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
47	MAX	chr11:67763921-67765083	A549	lung:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
48	MAX	chr11:67763867-67764879	K562	blood:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
49	MAZ	chr11:67764188-67764788	Hela-S3	cervix:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
50	MAZ	chr11:67764137-67764818	K562	blood:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67764320-67764370	HMEC	breast:	n/a
2	chr11:67764320-67764370	NH-A	brain:	n/a
3	chr11:67764320-67764370	PANC-1	pancreas:	n/a
4	chr11:67764654-67764704	BE2_C	brain:	n/a
5	chr11:67764320-67764370	Caco-2	colon:	n/a
6	chr11:67764654-67764704	HCF	heart:	n/a
7	chr11:67764320-67764370	ECC-1	luminal epithelium:	n/a
8	chr11:67764320-67764370	AG10803	skin:	n/a
9	chr11:67764654-67764704	IMR90	lung:	fetal
10	chr11:67764320-67764370	HAEpiC	amniotic membrane:	n/a
11	chr11:67764654-67764704	AG10803	skin:	n/a
12	chr11:67764654-67764704	AoSMC	blood vessel:	n/a
13	chr11:67764320-67764370	HNPCEpiC	eye:	n/a
14	chr11:67764320-67764370	BJ	skin:	n/a
15	chr11:67764320-67764370	GM06990	blood:	n/a
16	chr11:67764654-67764704	HMEC	breast:	n/a
17	chr11:67764320-67764370	HCM	heart:	n/a
18	chr11:67764320-67764370	HL-60	blood:	n/a
19	chr11:67764320-67764370	GM12878	blood:	n/a
20	chr11:67764320-67764370	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:67764320-67764370	LNCaP	prostate:	n/a
22	chr11:67764654-67764704	AG09309	skin:	n/a
23	chr11:67764320-67764370	HCPEpiC	choroid plexus:	n/a
24	chr11:67764654-67764704	SK-N-SH	brain:	n/a
25	chr11:67764654-67764704	HAEpiC	amniotic membrane:	n/a
26	chr11:67764320-67764370	HRE	kidney:	n/a
27	chr11:67764320-67764370	HCT-116	colon:	n/a
28	chr11:67764320-67764370	BE2_C	brain:	n/a
29	chr11:67764654-67764704	ovcar-3	ovarian:	n/a
30	chr11:67764654-67764704	HRCEpiC	kidney:	n/a
31	chr11:67764320-67764370	SK-N-SH	brain:	n/a
32	chr11:67764654-67764704	SAEC	small airway:	n/a
33	chr11:67764654-67764704	Caco-2	colon:	n/a
34	chr11:67764654-67764704	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:67764654-67764704	U87	brain:	n/a
36	chr11:67764654-67764704	Hepatocyte	liver:	n/a
37	chr11:67764320-67764370	MCF-7	breast:	n/a
38	chr11:67764320-67764370	HRCEpiC	kidney:	n/a
39	chr11:67764320-67764370	SKMC	muscle:	n/a
40	chr11:67764320-67764370	HCF	heart:	n/a
41	chr11:67764654-67764704	NHDF-neo	bronchial:	n/a
42	chr11:67764654-67764704	AG04449	skin:	fetal
43	chr11:67764654-67764704	HIPEpiC	eye:	n/a
44	chr11:67764654-67764704	ECC-1	luminal epithelium:	n/a
45	chr11:67764654-67764704	Jurkat	blood:	n/a
46	chr11:67764320-67764370	IMR90	lung:	fetal
47	chr11:67764320-67764370	MCF10A-Er-Src	breast:	n/a
48	chr11:67764654-67764704	NB4	blood:	n/a
49	chr11:67764654-67764704	HRE	kidney:	n/a
50	chr11:67764654-67764704	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67762605..67767485-chr11:67767779..67773135,10	K562	blood:
2	chr11:67763621..67766711-chr11:67769461..67772575,7	MCF-7	breast:
3	chr11:67762444..67764941-chr11:67774417..67777074,2	K562	blood:
4	chr11:67763215..67765770-chr11:68037604..68039605,2	K562	blood:
5	chr11:67764595..67767102-chr11:67888272..67890683,2	K562	blood:

Variant related genes	Relation type
UNC93B1	TF binding region
UNC93B1	CpG island
ENSG00000110057	chromatin interactions
ENSG00000255236	chromatin interactions
ENSG00000110721	chromatin interactions
ENSG00000006534	chromatin interactions
ENSG00000171067	chromatin interactions

Extended variants
information (count: 15 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527251071	chr11:67764327-67764328	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs552190505	chr11:67764408-67764409	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs570652487	chr11:67764429-67764430	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs114060891	chr11:67764447-67764448	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs114589544	chr11:67764464-67764465	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs61887536	chr11:67764517-67764518	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs556375296	chr11:67764519-67764520	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs568224747	chr11:67764529-67764530	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs535666095	chr11:67764564-67764565	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs148327744	chr11:67764635-67764636	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs572544777	chr11:67764662-67764663	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs2428815	chr11:67764663-67764664	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs55758147	chr11:67764681-67764682	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs34985263	chr11:67764695-67764696	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs558163630	chr11:67764697-67764698	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67759000-67766000	Weak transcription	Liver	Liver
2	chr11:67759200-67770400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr11:67759200-67770400	Weak transcription	Right Atrium	heart
4	chr11:67760200-67767600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr11:67761400-67769800	Genic enhancers	Primary B cells from peripheral blood	blood
6	chr11:67761600-67765600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr11:67761800-67764400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:67761800-67764800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:67761800-67765200	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr11:67761800-67765200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:67761800-67765400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr11:67761800-67765600	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr11:67761800-67765600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr11:67762000-67770400	Weak transcription	NHLF	lung
15	chr11:67762200-67764600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr11:67762200-67764800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr11:67762400-67764800	Weak transcription	Fetal Thymus	thymus
18	chr11:67762400-67765200	Weak transcription	Thymus	Thymus
19	chr11:67762400-67765600	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr11:67762600-67765400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr11:67762800-67767000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr11:67762800-67767200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr11:67763200-67764600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:67763400-67765200	Enhancers	Fetal Intestine Large	intestine
25	chr11:67763400-67767000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:67763600-67764400	Genic enhancers	Duodenum Mucosa	Duodenum
27	chr11:67763600-67766000	Genic enhancers	A549	lung
28	chr11:67763600-67766200	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr11:67763600-67769800	Genic enhancers	Primary monocytes fromperipheralblood	blood
30	chr11:67763800-67764400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:67763800-67766200	Genic enhancers	Primary B cells from cord blood	blood
32	chr11:67763800-67770400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr11:67764000-67764400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
34	chr11:67764000-67764400	Enhancers	Placenta	Placenta
35	chr11:67764000-67764400	Enhancers	Small Intestine	intestine
36	chr11:67764000-67764600	Enhancers	Brain Substantia Nigra	brain
37	chr11:67764000-67764800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
38	chr11:67764000-67764800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:67764000-67764800	Active TSS	H9 Cell Line	embryonic stem cell
40	chr11:67764000-67764800	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr11:67764000-67764800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:67764000-67764800	Flanking Active TSS	K562	blood
43	chr11:67764000-67765000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:67764000-67765000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr11:67764000-67765000	Enhancers	Stomach Mucosa	stomach
46	chr11:67764000-67765400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr11:67764000-67765600	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr11:67764000-67767400	Enhancers	Primary T cells fromperipheralblood	blood
49	chr11:67764000-67768400	Genic enhancers	GM12878-XiMat	blood
50	chr11:67764200-67764400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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