Variant report

Variant	nsv825996
Chromosome Location	chr11:75195626-75203332
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	ATF2	chr11:75201668-75202090	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr11:75203327-75203568	K562	blood:	n/a	n/a
3	BHLHE40	chr11:75203307-75203502	GM12878	blood:	n/a	n/a
4	BRCA1	chr11:75203178-75203352	GM12878	blood:	n/a	n/a
5	CEBPB	chr11:75201707-75201880	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr11:75201774-75202011	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr11:75201760-75201910	GM12867	blood:	n/a	n/a
8	E2F4	chr11:75195924-75196027	MCF10A-Er-Src	breast:	n/a	n/a
9	EGR1	chr11:75203223-75203446	K562	blood:	n/a	n/a
10	ELF1	chr11:75203055-75203647	GM12878	blood:	n/a	chr11:75203195-75203207 chr11:75203450-75203461 chr11:75203448-75203461
11	ELF1	chr11:75203255-75203651	GM12878	blood:	n/a	chr11:75203450-75203461 chr11:75203448-75203461
12	ELF1	chr11:75203298-75203626	A549	lung:	n/a	chr11:75203450-75203461 chr11:75203448-75203461
13	ELF1	chr11:75203171-75203705	MCF-7	breast:	n/a	chr11:75203195-75203207 chr11:75203450-75203461 chr11:75203448-75203461
14	ELF1	chr11:75203267-75203626	K562	blood:	n/a	chr11:75203450-75203461 chr11:75203448-75203461
15	ELF1	chr11:75203257-75203605	K562	blood:	n/a	chr11:75203450-75203461 chr11:75203448-75203461
16	FOS	chr11:75202539-75202621	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr11:75201721-75202000	MCF10A-Er-Src	breast:	n/a	chr11:75201859-75201867 chr11:75201857-75201868 chr11:75201857-75201869
18	FOS	chr11:75201695-75202043	MCF10A-Er-Src	breast:	n/a	chr11:75201859-75201867 chr11:75201857-75201868 chr11:75201857-75201869
19	FOS	chr11:75203330-75203508	MCF10A-Er-Src	breast:	n/a	chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203416-75203427 chr11:75203420-75203429 chr11:75203406-75203415
20	FOS	chr11:75203300-75203609	MCF10A-Er-Src	breast:	n/a	chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203416-75203427 chr11:75203420-75203429 chr11:75203406-75203415
21	FOS	chr11:75201731-75202000	MCF10A-Er-Src	breast:	n/a	chr11:75201859-75201867 chr11:75201857-75201868 chr11:75201857-75201869
22	FOS	chr11:75201804-75202002	MCF10A-Er-Src	breast:	n/a	chr11:75201859-75201867 chr11:75201857-75201868 chr11:75201857-75201869
23	FOS	chr11:75201707-75202068	HUVEC	blood vessel:	n/a	chr11:75201859-75201867 chr11:75201857-75201868 chr11:75201857-75201869
24	FOS	chr11:75203318-75203553	MCF10A-Er-Src	breast:	n/a	chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203416-75203427 chr11:75203420-75203429 chr11:75203406-75203415
25	FOSL1	chr11:75201781-75201987	K562	blood:	n/a	chr11:75201857-75201868 chr11:75201859-75201867 chr11:75201857-75201869
26	FOSL2	chr11:75201710-75202096	A549	lung:	n/a	chr11:75201859-75201867 chr11:75201857-75201869
27	FOSL2	chr11:75201598-75202117	SK-N-SH	brain:	n/a	chr11:75201859-75201867 chr11:75201857-75201869
28	GABPA	chr11:75203269-75203581	GM12878	blood:	n/a	n/a
29	GABPA	chr11:75203119-75203642	K562	blood:	n/a	n/a
30	GABPA	chr11:75203219-75203681	A549	lung:	n/a	n/a
31	GABPA	chr11:75203229-75203669	Hela-S3	cervix:	n/a	n/a
32	GABPA	chr11:75203290-75203633	A549	lung:	n/a	n/a
33	GABPA	chr11:75203184-75203698	MCF-7	breast:	n/a	n/a
34	GABPA	chr11:75203166-75203746	HL-60	blood:	n/a	n/a
35	GABPA	chr11:75203241-75203602	K562	blood:	n/a	n/a
36	GABPA	chr11:75203312-75203538	Hela-S3	cervix:	n/a	n/a
37	GABPA	chr11:75203193-75203777	HL-60	blood:	n/a	n/a
38	JUN	chr11:75201710-75202069	H1-hESC	embryonic stem cell:	n/a	chr11:75201859-75201867 chr11:75201857-75201869
39	JUND	chr11:75201634-75202022	H1-hESC	embryonic stem cell:	n/a	chr11:75201859-75201867 chr11:75201857-75201869
40	JUND	chr11:75203275-75203546	K562	blood:	n/a	chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203419-75203429 chr11:75203416-75203427 chr11:75203420-75203429 chr11:75203406-75203415
41	JUND	chr11:75201667-75202101	H1-hESC	embryonic stem cell:	n/a	chr11:75201859-75201867 chr11:75201857-75201869
42	JUND	chr11:75201476-75202202	SK-N-SH	brain:	n/a	chr11:75201859-75201867 chr11:75201857-75201869
43	JUND	chr11:75201679-75202056	A549	lung:	n/a	chr11:75201859-75201867 chr11:75201857-75201869
44	JUND	chr11:75201680-75202003	H1-hESC	embryonic stem cell:	n/a	chr11:75201859-75201867 chr11:75201857-75201869
45	MAX	chr11:75203244-75203668	NB4	blood:	n/a	n/a
46	MAX	chr11:75203290-75203592	K562	blood:	n/a	n/a
47	MYC	chr11:75201846-75201926	HUVEC	blood vessel:	n/a	n/a
48	MYC	chr11:75203305-75203647	NB4	blood:	n/a	n/a
49	MYC	chr11:75203327-75203333	MCF-7	breast:	n/a	n/a
50	MYC	chr11:75203265-75203291	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75201685-75201735	BJ	skin:	n/a
2	chr11:75201685-75201735	NHDF-neo	bronchial:	n/a
3	chr11:75201685-75201735	ECC-1	luminal epithelium:	n/a
4	chr11:75201685-75201735	SK-N-MC	brain:	n/a
5	chr11:75201685-75201735	HRE	kidney:	n/a
6	chr11:75201685-75201735	NH-A	brain:	n/a
7	chr11:75201685-75201735	HRPEpiC	eye:	n/a
8	chr11:75201685-75201735	HCF	heart:	n/a
9	chr11:75201685-75201735	SKMC	muscle:	n/a
10	chr11:75201685-75201735	HNPCEpiC	eye:	n/a
11	chr11:75201685-75201735	GM12892	blood:	n/a
12	chr11:75201685-75201735	Caco-2	colon:	n/a
13	chr11:75201685-75201735	GM12878	blood:	n/a
14	chr11:75201685-75201735	BE2_C	brain:	n/a
15	chr11:75201685-75201735	ProgFib	skin:	n/a
16	chr11:75201685-75201735	HMEC	breast:	n/a
17	chr11:75201685-75201735	AG04449	skin:	fetal
18	chr11:75201685-75201735	AoSMC	blood vessel:	n/a
19	chr11:75201685-75201735	PrEC	prostate:	n/a
20	chr11:75201685-75201735	T-47D	breast:	n/a
21	chr11:75201685-75201735	NB4	blood:	n/a
22	chr11:75201685-75201735	RPTEC	kidney:	n/a
23	chr11:75201685-75201735	AG09309	skin:	n/a
24	chr11:75201685-75201735	SAEC	small airway:	n/a
25	chr11:75201685-75201735	IMR90	lung:	fetal
26	chr11:75201685-75201735	PANC-1	pancreas:	n/a
27	chr11:75201685-75201735	K562	blood:	n/a
28	chr11:75201685-75201735	SK-N-SH_RA	brain:	n/a
29	chr11:75201685-75201735	GM06990	blood:	n/a
30	chr11:75201685-75201735	HCM	heart:	n/a
31	chr11:75201685-75201735	HRCEpiC	kidney:	n/a
32	chr11:75201685-75201735	H1-hESC	embryonic stem cell:	embryo
33	chr11:75201685-75201735	HEK293	kidney:	embryo
34	chr11:75201685-75201735	AG10803	skin:	n/a
35	chr11:75201685-75201735	HL-60	blood:	n/a
36	chr11:75201685-75201735	AG09319	gingival:	n/a
37	chr11:75201685-75201735	Hela-S3	cervix:	n/a
38	chr11:75201685-75201735	NHBE	bronchial:	n/a
39	chr11:75201685-75201735	HEEpiC	esophagus:	n/a
40	chr11:75201685-75201735	ovcar-3	ovarian:	n/a
41	chr11:75201685-75201735	Hepatocyte	liver:	n/a
42	chr11:75201685-75201735	HAEpiC	amniotic membrane:	n/a
43	chr11:75201685-75201735	HCPEpiC	choroid plexus:	n/a
44	chr11:75201685-75201735	HCT-116	colon:	n/a
45	chr11:75201685-75201735	HUVEC	blood vessel:	n/a
46	chr11:75201685-75201735	MCF-7	breast:	n/a
47	chr11:75201685-75201735	GM19239	blood:	n/a
48	chr11:75201685-75201735	GM12891	blood:	n/a
49	chr11:75201685-75201735	HepG2	liver:	n/a
50	chr11:75201685-75201735	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:75196048..75198096-chr11:75221124..75222678,2	MCF-7	breast:
2	chr11:75186423..75188493-chr11:75202325..75205145,2	K562	blood:
3	chr11:75196940..75199795-chr11:75215143..75217908,2	K562	blood:
4	chr11:75139447..75142443-chr11:75197047..75198712,2	MCF-7	breast:
5	chr11:75185809..75187737-chr11:75194465..75195996,2	K562	blood:
6	chr11:75203200..75205117-chr11:75206279..75208422,2	MCF-7	breast:
7	chr11:75202940..75204464-chr11:75209500..75211854,2	MCF-7	breast:
8	chr11:75189305..75191743-chr11:75201483..75203420,3	K562	blood:
9	chr11:75191759..75194523-chr11:75195624..75199123,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL35-4	chr11:75201282-75201365	NONHSAT023105
2	lnc-KLHL35-4	chr11:75196350-75196786	NONHSAT023105

Variant related genes	Relation type
GDPD5	TF binding region
GDPD5	CpG island
ENSG00000158555	chromatin interactions
ENSG00000149243	chromatin interactions

Extended variants
information (count: 262 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189407382	chr11:75195643-75195644	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532294177	chr11:75195644-75195645	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77447468	chr11:75195696-75195697	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563081298	chr11:75195782-75195783	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531907020	chr11:75195816-75195817	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371770131	chr11:75195817-75195818	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548885314	chr11:75195840-75195841	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181418393	chr11:75195862-75195863	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534487299	chr11:75195869-75195870	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535349436	chr11:75195921-75195922	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547513433	chr11:75195934-75195935	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527892109	chr11:75195950-75195951	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375053733	chr11:75195966-75195967	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570507059	chr11:75196072-75196073	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539557636	chr11:75196109-75196110	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549557893	chr11:75196148-75196149	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556207707	chr11:75196170-75196171	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140437876	chr11:75196171-75196172	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369096700	chr11:75196194-75196195	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369705562	chr11:75196217-75196218	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75061966	chr11:75196239-75196240	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548515416	chr11:75196327-75196328	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537673207	chr11:75196352-75196353	Weak transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs185183885	chr11:75196355-75196356	Weak transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs150406698	chr11:75196433-75196434	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs561607769	chr11:75196493-75196494	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs560192786	chr11:75196509-75196510	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs370739770	chr11:75196555-75196556	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs148453115	chr11:75196556-75196557	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs3138546	chr11:75196557-75196558	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs59171796	chr11:75196594-75196595	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs576866627	chr11:75196597-75196598	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs532039902	chr11:75196607-75196608	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs549934315	chr11:75196608-75196609	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs368416247	chr11:75196661-75196662	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs546943186	chr11:75196729-75196730	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs189833791	chr11:75196735-75196736	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs138195130	chr11:75196740-75196741	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs562540887	chr11:75196794-75196795	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531411372	chr11:75196828-75196829	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568467722	chr11:75196843-75196844	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181436680	chr11:75196867-75196868	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114885703	chr11:75196869-75196870	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528019499	chr11:75196882-75196883	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547647177	chr11:75196887-75196888	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570529009	chr11:75196932-75196933	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571892672	chr11:75197018-75197019	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186027199	chr11:75197026-75197027	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs60616589	chr11:75197070-75197071	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535935629	chr11:75197224-75197225	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Usher syndrome	18421352	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75187000-75201400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:75187200-75201200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr11:75187200-75203000	Weak transcription	Primary T cells from cord blood	blood
4	chr11:75187400-75198200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:75187400-75202800	Weak transcription	Primary B cells from peripheral blood	blood
6	chr11:75187400-75202800	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr11:75187400-75202800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr11:75187400-75203000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr11:75187600-75201000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:75187600-75202000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr11:75187800-75201000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:75188000-75201600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr11:75188200-75200400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr11:75188400-75201200	Weak transcription	HSMM	muscle
15	chr11:75188400-75201400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr11:75188400-75201400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr11:75188400-75201600	Weak transcription	HSMMtube	muscle
18	chr11:75188600-75201600	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr11:75190400-75199000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr11:75190400-75199200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:75190400-75207400	Weak transcription	Fetal Stomach	stomach
22	chr11:75190800-75201600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr11:75191000-75196800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:75192200-75202800	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr11:75192400-75198200	Weak transcription	Fetal Intestine Large	intestine
26	chr11:75193000-75203200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr11:75193800-75196200	Enhancers	Liver	Liver
28	chr11:75193800-75203200	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr11:75194000-75196800	Enhancers	HepG2	liver
30	chr11:75194000-75203000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr11:75194200-75197200	Weak transcription	Psoas Muscle	Psoas
32	chr11:75194400-75197800	Weak transcription	Brain Germinal Matrix	brain
33	chr11:75194600-75196600	Weak transcription	Fetal Muscle Trunk	muscle
34	chr11:75194600-75197600	Weak transcription	Placenta	Placenta
35	chr11:75194600-75198200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr11:75194600-75203000	Weak transcription	Lung	lung
37	chr11:75194800-75198600	Weak transcription	Adipose Nuclei	Adipose
38	chr11:75195000-75201200	Weak transcription	Spleen	Spleen
39	chr11:75195200-75195800	Strong transcription	Fetal Intestine Small	intestine
40	chr11:75195800-75196400	Genic enhancers	Fetal Intestine Small	intestine
41	chr11:75196400-75202200	Strong transcription	Fetal Intestine Small	intestine
42	chr11:75196600-75197000	Enhancers	Fetal Muscle Trunk	muscle
43	chr11:75196800-75197400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr11:75196800-75199000	Weak transcription	HepG2	liver
45	chr11:75197600-75197800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr11:75197600-75198200	Strong transcription	Placenta	Placenta
47	chr11:75197800-75201400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr11:75197800-75201600	Enhancers	Brain Germinal Matrix	brain
49	chr11:75198000-75198200	Enhancers	Right Ventricle	heart
50	chr11:75198000-75201000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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