Variant report

Variant	nsv897030
Chromosome Location	chr11:19049478-19106045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:894)
CpG islands
(count:368)
Chromatin interactive
region (count:36)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:894 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:19093741-19093747	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:19092648-19093101	K562	blood:	n/a	n/a
3	ARID3A	chr11:19092647-19093076	HepG2	liver:	n/a	n/a
4	ATF1	chr11:19092747-19093100	K562	blood:	n/a	n/a
5	ATF2	chr11:19092649-19093135	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:19092639-19093114	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr11:19092631-19093067	GM12878	blood:	n/a	n/a
8	ATF3	chr11:19092741-19093094	K562	blood:	n/a	chr11:19092868-19092879 chr11:19092870-19092878 chr11:19092868-19092879 chr11:19092868-19092881
9	ATF3	chr11:19101093-19101693	HCT-116	colon:	n/a	n/a
10	ATF3	chr11:19092685-19093129	GM12878	blood:	n/a	chr11:19092868-19092879 chr11:19092870-19092878 chr11:19092868-19092879 chr11:19092868-19092881
11	BACH1	chr11:19092773-19093119	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr11:19092683-19093118	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:19092747-19093102	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:19093563-19093861	HepG2	liver:	n/a	n/a
15	BHLHE40	chr11:19093331-19093466	K562	blood:	n/a	n/a
16	BRCA1	chr11:19098596-19098796	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr11:19092708-19093152	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr11:19092764-19092957	HepG2	liver:	n/a	n/a
19	CBX3	chr11:19092724-19093146	K562	blood:	n/a	n/a
20	CBX3	chr11:19100880-19101745	HCT-116	colon:	n/a	n/a
21	CBX3	chr11:19049746-19050118	HCT-116	colon:	n/a	n/a
22	CBX3	chr11:19092718-19092997	K562	blood:	n/a	n/a
23	CBX3	chr11:19092602-19093253	HCT-116	colon:	n/a	n/a
24	CEBPB	chr11:19101233-19101561	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr11:19070915-19071272	IMR90	lung:	n/a	chr11:19071079-19071090
26	CEBPB	chr11:19093404-19093603	K562	blood:	n/a	n/a
27	CEBPB	chr11:19100977-19101709	HCT-116	colon:	n/a	n/a
28	CEBPB	chr11:19070928-19071245	K562	blood:	n/a	chr11:19071079-19071090
29	CEBPB	chr11:19075539-19075817	IMR90	lung:	n/a	chr11:19075655-19075666
30	CEBPB	chr11:19092715-19093066	HepG2	liver:	n/a	n/a
31	CEBPB	chr11:19070928-19071353	HepG2	liver:	n/a	chr11:19071079-19071090
32	CEBPB	chr11:19092733-19093067	K562	blood:	n/a	n/a
33	CEBPB	chr11:19098572-19098738	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr11:19095795-19096042	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr11:19075511-19075778	K562	blood:	n/a	chr11:19075655-19075666
36	CEBPB	chr11:19101189-19101545	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:19092730-19093077	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:19075503-19075812	HepG2	liver:	n/a	chr11:19075655-19075666
39	CEBPB	chr11:19070945-19071259	Hela-S3	cervix:	n/a	chr11:19071079-19071090
40	CEBPB	chr11:19095826-19096026	A549	lung:	n/a	n/a
41	CEBPB	chr11:19101171-19101670	MCF-7	breast:	n/a	n/a
42	CEBPB	chr11:19075550-19075793	A549	lung:	n/a	chr11:19075655-19075666
43	CEBPB	chr11:19092787-19093018	K562	blood:	n/a	n/a
44	CEBPB	chr11:19049458-19049658	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr11:19070911-19071248	H1-hESC	embryonic stem cell:	n/a	chr11:19071079-19071090
46	CEBPB	chr11:19101156-19101610	MCF-7	breast:	n/a	n/a
47	CEBPB	chr11:19101019-19101937	HCT-116	colon:	n/a	n/a
48	CEBPB	chr11:19070943-19071260	A549	lung:	n/a	chr11:19071079-19071090
49	CEBPB	chr11:19092703-19093066	A549	lung:	n/a	n/a
50	CEBPB	chr11:19070121-19070197	H1-hESC	embryonic stem cell:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:19078052-19078102	GM12878	blood:	n/a
2	chr11:19077763-19077813	AG04449	skin:	fetal
3	chr11:19078052-19078102	GM12878	blood:	n/a
4	chr11:19077763-19077813	AG04449	skin:	fetal
5	chr11:19081590-19081640	BE2_C	brain:	n/a
6	chr11:19081590-19081640	HEK293	kidney:	embryo
7	chr11:19077763-19077813	HL-60	blood:	n/a
8	chr11:19083542-19083592	HCM	heart:	n/a
9	chr11:19081590-19081640	HEEpiC	esophagus:	n/a
10	chr11:19081590-19081640	HUVEC	blood vessel:	n/a
11	chr11:19078052-19078102	GM12891	blood:	n/a
12	chr11:19095211-19095261	HIPEpiC	eye:	n/a
13	chr11:19095211-19095261	HL-60	blood:	n/a
14	chr11:19077763-19077813	Caco-2	colon:	n/a
15	chr11:19095211-19095261	NHDF-neo	bronchial:	n/a
16	chr11:19077763-19077813	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:19095211-19095261	HRE	kidney:	n/a
18	chr11:19081590-19081640	SK-N-SH_RA	brain:	n/a
19	chr11:19082514-19082564	T-47D	breast:	n/a
20	chr11:19077763-19077813	Hepatocyte	liver:	n/a
21	chr11:19077763-19077813	GM12892	blood:	n/a
22	chr11:19095211-19095261	K562	blood:	n/a
23	chr11:19078052-19078102	SKMC	muscle:	n/a
24	chr11:19081590-19081640	AG04449	skin:	fetal
25	chr11:19077763-19077813	AG04450	lung:	fetal
26	chr11:19078052-19078102	NH-A	brain:	n/a
27	chr11:19081590-19081640	GM12892	blood:	n/a
28	chr11:19095211-19095261	GM06990	blood:	n/a
29	chr11:19083542-19083592	SK-N-SH	brain:	n/a
30	chr11:19095211-19095261	PANC-1	pancreas:	n/a
31	chr11:19077763-19077813	HNPCEpiC	eye:	n/a
32	chr11:19082514-19082564	NT2-D1	testis:	n/a
33	chr11:19077763-19077813	H1-hESC	embryonic stem cell:	embryo
34	chr11:19081590-19081640	HIPEpiC	eye:	n/a
35	chr11:19077763-19077813	BJ	skin:	n/a
36	chr11:19095211-19095261	U87	brain:	n/a
37	chr11:19077763-19077813	NHDF-neo	bronchial:	n/a
38	chr11:19078052-19078102	U87	brain:	n/a
39	chr11:19095211-19095261	ECC-1	luminal epithelium:	n/a
40	chr11:19077763-19077813	AG10803	skin:	n/a
41	chr11:19082514-19082564	Caco-2	colon:	n/a
42	chr11:19078052-19078102	AG04450	lung:	fetal
43	chr11:19078052-19078102	PrEC	prostate:	n/a
44	chr11:19081590-19081640	AoSMC	blood vessel:	n/a
45	chr11:19081590-19081640	HCM	heart:	n/a
46	chr11:19078052-19078102	IMR90	lung:	fetal
47	chr11:19077763-19077813	T-47D	breast:	n/a
48	chr11:19082514-19082564	MCF-7	breast:	n/a
49	chr11:19083542-19083592	HPAEpiC	pulmonary alveolar:	n/a
50	chr11:19078052-19078102	K562	blood:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:19099395..19100355-chr2:160311941..160312802,2	MCF-7	breast:
2	chr11:19100832..19103167-chr11:19106343..19107943,2	K562	blood:
3	chr11:19096399..19098941-chr11:19128925..19131186,2	MCF-7	breast:
4	chr11:19093222..19095138-chr11:19125990..19128293,2	MCF-7	breast:
5	chr11:19092805..19093359-chr11:19763994..19764827,2	MCF-7	breast:
6	chr11:19092484..19094846-chr11:19096156..19098835,2	MCF-7	breast:
7	chr11:19098962..19100947-chr11:19123727..19125243,2	MCF-7	breast:
8	chr10:35195660..35196160-chr11:19092631..19093233,2	MCF-7	breast:
9	chr11:19092311..19093429-chr11:19574985..19576236,16	MCF-7	breast:
10	chr11:19097989..19099036-chr11:19138658..19139431,4	MCF-7	breast:
11	chr11:19098280..19099189-chr11:19131718..19132697,3	MCF-7	breast:
12	chr11:19092360..19092956-chr11:19138799..19139467,2	MCF-7	breast:
13	chr11:19091906..19093550-chr11:19574860..19576001,19	K562	blood:
14	chr10:35195660..35196180-chr11:19092642..19093348,2	MCF-7	breast:
15	chr11:19098252..19099216-chr11:19574958..19576000,3	K562	blood:
16	chr11:19092526..19093289-chr11:19182527..19183071,2	MCF-7	breast:
17	chr11:19092338..19093322-chr11:19281072..19281919,3	K562	blood:
18	chr11:19081397..19083267-chr11:19138143..19140482,2	MCF-7	breast:
19	chr11:19094423..19096324-chr11:19165752..19167827,2	MCF-7	breast:
20	chr11:19092645..19093311-chr5:141695576..141696096,4	MCF-7	breast:
21	chr11:19101141..19102914-chr11:19106636..19109089,2	MCF-7	breast:
22	chr11:19092482..19093281-chr11:19347628..19348265,2	MCF-7	breast:
23	chr11:19101207..19103376-chr11:19137461..19139475,2	MCF-7	breast:
24	chr11:19092362..19093374-chr11:19131560..19132799,3	MCF-7	breast:
25	chr11:18948757..18949726-chr11:19092570..19093333,3	MCF-7	breast:
26	chr11:19092474..19093535-chr11:19131007..19132483,9	MCF-7	breast:
27	chr11:19092510..19093247-chr11:19579344..19580002,2	MCF-7	breast:
28	chr11:19092441..19093031-chr11:19138770..19139494,2	K562	blood:
29	chr11:19092701..19093408-chr11:19575271..19576064,4	MCF-7	breast:
30	chr11:19098389..19099222-chr11:19131553..19132388,4	MCF-7	breast:
31	chr11:19092484..19094846-chr11:19096156..19098835,2	MCF-7	breast:
32	chr11:19092467..19093363-chr11:19280997..19281539,2	MCF-7	breast:
33	chr11:19098344..19099098-chr11:19575067..19575905,2	MCF-7	breast:
34	chr11:19092409..19092994-chr11:19579154..19579874,2	K562	blood:
35	chr11:19093295..19097207-chr11:19260781..19264758,3	K562	blood:
36	chr11:19092605..19093423-chr11:19578784..19579949,4	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRGPRX2-1	chr11:19051244-19051985	NONHSAT018325

No data

Variant related genes	Relation type
ENSG00000255424	TF binding region
MRGPRX2	TF binding region
ENSG00000255424	CpG island
MRGPRX2	CpG island
ENSG00000177054	chromatin interactions
ENSG00000129173	chromatin interactions

Extended variants
information (count: 907 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:907 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1039516	chr11:19049478-19049479	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117722667	chr11:19049499-19049500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374034823	chr11:19049505-19049506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142702575	chr11:19049574-19049575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575263589	chr11:19049583-19049584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs58289452	chr11:19049610-19049611	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs180992452	chr11:19049637-19049638	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs75633469	chr11:19049678-19049679	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs371996574	chr11:19049730-19049731	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs573307505	chr11:19049748-19049749	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs185282869	chr11:19049765-19049766	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs562481886	chr11:19049776-19049777	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs540422747	chr11:19049778-19049779	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs545306617	chr11:19049807-19049808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555247931	chr11:19049828-19049829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs80315468	chr11:19049835-19049836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531201725	chr11:19049873-19049874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549725767	chr11:19049891-19049892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs151021350	chr11:19049895-19049896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368770181	chr11:19049923-19049924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115396872	chr11:19049940-19049941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188583730	chr11:19049948-19049949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538764109	chr11:19049963-19049964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552903796	chr11:19050015-19050016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181342316	chr11:19050028-19050029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563601716	chr11:19050117-19050118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs61580154	chr11:19050118-19050119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565482085	chr11:19050182-19050183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530694364	chr11:19050194-19050195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375758959	chr11:19050195-19050196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185865744	chr11:19050225-19050226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554486464	chr11:19050259-19050260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577467431	chr11:19050265-19050266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192002826	chr11:19050314-19050315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7942424	chr11:19050331-19050332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576838424	chr11:19050346-19050347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549213317	chr11:19050347-19050348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11825508	chr11:19050354-19050355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563260835	chr11:19050356-19050357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545244320	chr11:19050361-19050362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529749939	chr11:19050393-19050394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs67345452	chr11:19050398-19050399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150149119	chr11:19050399-19050400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575192453	chr11:19050417-19050418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377720977	chr11:19050427-19050428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114911956	chr11:19050465-19050466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571761054	chr11:19050473-19050474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532618691	chr11:19050560-19050561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550698905	chr11:19050572-19050573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147814297	chr11:19050574-19050575	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:19046600-19050600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr11:19047200-19050000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:19048400-19049800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:19048400-19050800	Enhancers	NHEK	skin
5	chr11:19048600-19049600	Weak transcription	Stomach Mucosa	stomach
6	chr11:19048600-19050600	Enhancers	HMEC	breast
7	chr11:19048800-19049600	Weak transcription	NHDF-Ad	bronchial
8	chr11:19048800-19050000	Enhancers	NH-A	brain
9	chr11:19048800-19050600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:19048800-19050600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:19049400-19049800	Enhancers	Hela-S3	cervix
12	chr11:19049600-19049800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:19049600-19049800	Enhancers	HUVEC	blood vessel
14	chr11:19049600-19049800	Enhancers	NHDF-Ad	bronchial
15	chr11:19049600-19049800	Flanking Active TSS	Osteobl	bone
16	chr11:19049600-19050000	Enhancers	Muscle Satellite Cultured Cells	--
17	chr11:19049600-19050000	Enhancers	Esophagus	oesophagus
18	chr11:19049600-19050000	Enhancers	Stomach Mucosa	stomach
19	chr11:19049800-19050400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr11:19050400-19051800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:19051200-19051800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:19076200-19076800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:19076800-19077000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr11:19077000-19077400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:19077400-19077600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:19077400-19077800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr11:19079000-19079400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:19079200-19079800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr11:19081200-19083600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:19081400-19083400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:19081400-19083800	Enhancers	Primary T cells fromperipheralblood	blood
32	chr11:19081400-19083800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr11:19081800-19083600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:19081800-19083800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr11:19082000-19083000	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr11:19082000-19083200	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr11:19082000-19083400	Enhancers	Primary hematopoietic stem cells	blood
38	chr11:19082000-19083400	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr11:19082000-19083600	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr11:19082200-19082400	Bivalent Enhancer	Dnd41	blood
41	chr11:19082200-19082600	Bivalent Enhancer	HUVEC	blood vessel
42	chr11:19082200-19083200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr11:19082200-19083400	Enhancers	Primary T cells from cord blood	blood
44	chr11:19082200-19083400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr11:19091000-19094000	Weak transcription	Pancreas	Pancrea
46	chr11:19091600-19094000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:19092600-19093200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr11:19092800-19093000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:19092800-19093000	Active TSS	Duodenum Mucosa	Duodenum
50	chr11:19092800-19093000	Enhancers	Fetal Muscle Trunk	muscle

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