Variant report

Variant	esv1810299
Chromosome Location	chr6:26905022-26967897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1246)
CpG islands
(count:244)
Chromatin interactive
region (count:6)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1246 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26925619-26925955	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:26924747-26924778	HepG2	liver:	n/a	n/a
3	ATF1	chr6:26923925-26924305	K562	blood:	n/a	n/a
4	ATF2	chr6:26923942-26924231	GM12878	blood:	n/a	n/a
5	ATF2	chr6:26923847-26924306	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:26923841-26924229	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:26924664-26924943	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr6:26923787-26924103	GM12878	blood:	n/a	n/a
9	BATF	chr6:26929003-26929176	GM12878	blood:	n/a	chr6:26929117-26929127 chr6:26929116-26929127
10	BATF	chr6:26923753-26924403	GM12878	blood:	n/a	n/a
11	BATF	chr6:26917064-26917394	GM12878	blood:	n/a	n/a
12	BATF	chr6:26918546-26918790	GM12878	blood:	n/a	n/a
13	BATF	chr6:26928990-26929230	GM12878	blood:	n/a	chr6:26929117-26929127 chr6:26929116-26929127
14	BATF	chr6:26925319-26925723	GM12878	blood:	n/a	n/a
15	BATF	chr6:26920524-26920940	GM12878	blood:	n/a	n/a
16	BATF	chr6:26921657-26921936	GM12878	blood:	n/a	n/a
17	BATF	chr6:26911356-26911600	GM12878	blood:	n/a	n/a
18	BATF	chr6:26940264-26940496	GM12878	blood:	n/a	chr6:26940350-26940360
19	BATF	chr6:26919159-26919394	GM12878	blood:	n/a	n/a
20	BATF	chr6:26949170-26949399	GM12878	blood:	n/a	chr6:26949247-26949258
21	BATF	chr6:26922534-26922741	GM12878	blood:	n/a	n/a
22	BATF	chr6:26923172-26923556	GM12878	blood:	n/a	n/a
23	BATF	chr6:26919077-26919488	GM12878	blood:	n/a	n/a
24	BATF	chr6:26925030-26925340	GM12878	blood:	n/a	n/a
25	BATF	chr6:26917548-26917891	GM12878	blood:	n/a	n/a
26	BATF	chr6:26924423-26924966	GM12878	blood:	n/a	n/a
27	BATF	chr6:26923128-26923365	GM12878	blood:	n/a	n/a
28	BATF	chr6:26911148-26911328	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:26926995-26927272	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:26928918-26929198	GM12878	blood:	n/a	chr6:26929119-26929128 chr6:26929120-26929129
31	BCL11A	chr6:26920970-26921280	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:26917588-26917845	GM12878	blood:	n/a	n/a
33	BCL11A	chr6:26917579-26917780	GM12878	blood:	n/a	n/a
34	BCL11A	chr6:26918589-26918831	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:26923669-26925780	GM12878	blood:	n/a	n/a
36	BCL11A	chr6:26923081-26923566	GM12878	blood:	n/a	n/a
37	BCL11A	chr6:26924092-26924992	GM12878	blood:	n/a	n/a
38	BCL11A	chr6:26917021-26917371	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:26917073-26917429	GM12878	blood:	n/a	n/a
40	BCL11A	chr6:26910854-26911026	GM12878	blood:	n/a	n/a
41	BCL11A	chr6:26928959-26929218	GM12878	blood:	n/a	chr6:26929119-26929128 chr6:26929120-26929129
42	BCL11A	chr6:26919192-26919425	GM12878	blood:	n/a	n/a
43	BCL11A	chr6:26925060-26925245	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:26922379-26922777	GM12878	blood:	n/a	n/a
45	BCL11A	chr6:26921673-26921928	GM12878	blood:	n/a	n/a
46	BCL11A	chr6:26923759-26924025	GM12878	blood:	n/a	n/a
47	BCL11A	chr6:26965321-26965485	GM12878	blood:	n/a	n/a
48	BCLAF1	chr6:26924603-26924888	GM12878	blood:	n/a	n/a
49	BCLAF1	chr6:26923808-26924142	K562	blood:	n/a	n/a
50	BCLAF1	chr6:26924598-26924962	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26924550-26924600	HNPCEpiC	eye:	n/a
2	chr6:26924767-26924817	IMR90	lung:	fetal
3	chr6:26924767-26924817	GM12891	blood:	n/a
4	chr6:26914441-26914491	SK-N-SH	brain:	n/a
5	chr6:26924767-26924817	Jurkat	blood:	n/a
6	chr6:26923983-26924033	SKMC	muscle:	n/a
7	chr6:26924767-26924817	GM12878	blood:	n/a
8	chr6:26924767-26924817	Hela-S3	cervix:	n/a
9	chr6:26914441-26914491	AG04450	lung:	fetal
10	chr6:26924767-26924817	GM19239	blood:	n/a
11	chr6:26914441-26914491	HPAEpiC	pulmonary alveolar:	n/a
12	chr6:26914441-26914491	H1-hESC	embryonic stem cell:	embryo
13	chr6:26924767-26924817	AG10803	skin:	n/a
14	chr6:26924550-26924600	NB4	blood:	n/a
15	chr6:26914441-26914491	CMK	blood:	n/a
16	chr6:26924550-26924600	Hela-S3	cervix:	n/a
17	chr6:26914441-26914491	HAEpiC	amniotic membrane:	n/a
18	chr6:26924767-26924817	PFSK-1	brain:	n/a
19	chr6:26923983-26924033	ovcar-3	ovarian:	n/a
20	chr6:26923983-26924033	SK-N-MC	brain:	n/a
21	chr6:26924550-26924600	PFSK-1	brain:	n/a
22	chr6:26914441-26914491	NHBE	bronchial:	n/a
23	chr6:26923983-26924033	Jurkat	blood:	n/a
24	chr6:26923983-26924033	PFSK-1	brain:	n/a
25	chr6:26923983-26924033	GM12892	blood:	n/a
26	chr6:26924767-26924817	HNPCEpiC	eye:	n/a
27	chr6:26924550-26924600	HEK293	kidney:	embryo
28	chr6:26914441-26914491	NB4	blood:	n/a
29	chr6:26924767-26924817	SK-N-SH	brain:	n/a
30	chr6:26923983-26924033	LNCaP	prostate:	n/a
31	chr6:26914441-26914491	GM12878	blood:	n/a
32	chr6:26923983-26924033	NT2-D1	testis:	n/a
33	chr6:26923983-26924033	GM12878	blood:	n/a
34	chr6:26924550-26924600	HRCEpiC	kidney:	n/a
35	chr6:26924550-26924600	ovcar-3	ovarian:	n/a
36	chr6:26914441-26914491	HRCEpiC	kidney:	n/a
37	chr6:26914441-26914491	HUVEC	blood vessel:	n/a
38	chr6:26924767-26924817	PrEC	prostate:	n/a
39	chr6:26923983-26924033	HEEpiC	esophagus:	n/a
40	chr6:26924767-26924817	RPTEC	kidney:	n/a
41	chr6:26924550-26924600	MCF-7	breast:	n/a
42	chr6:26914441-26914491	HCM	heart:	n/a
43	chr6:26924550-26924600	HRE	kidney:	n/a
44	chr6:26924550-26924600	AG09319	gingival:	n/a
45	chr6:26924550-26924600	T-47D	breast:	n/a
46	chr6:26924767-26924817	HepG2	liver:	n/a
47	chr6:26924767-26924817	ProgFib	skin:	n/a
48	chr6:26914441-26914491	AG10803	skin:	n/a
49	chr6:26924767-26924817	NT2-D1	testis:	n/a
50	chr6:26924550-26924600	ProgFib	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26962343..26965289-chr6:26986491..26988275,2	MCF-7	breast:
2	chr6:26922448..26924229-chr6:27062597..27064654,2	K562	blood:
3	chr6:26923847..26925381-chr6:26927830..26930168,2	MCF-7	breast:
4	chr6:26923074..26925467-chr6:26986570..26988926,2	K562	blood:
5	chr6:26156738..26158730-chr6:26923909..26926382,2	K562	blood:
6	chr6:26922078..26923970-chr6:27032946..27034480,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST1H2AG-3	chr6:26936241-26936301	NONHSAT108319
2	lnc-HIST1H2AG-3	chr6:26926892-26926895	NONHSAT108319
3	lnc-HIST1H2AG-3	chr6:26936237-26936301	ENSG00000224843.2
4	lnc-HIST1H2AG-3	chr6:26936797-26942146	ENSG00000224843.2
5	lnc-HIST1H2AG-3	chr6:26936237-26936301	XLOC_005216
6	lnc-HIST1H2AG-3	chr6:26936797-26936850	XLOC_005216
7	lnc-HIST1H2AG-3	chr6:26936237-26936301	NONHSAT108320
8	lnc-HIST1H2AG-3	chr6:26936237-26936301	ENSG00000224843.2
9	lnc-HIST1H2AG-3	chr6:26924772-26924962	ENSG00000224843.2
10	lnc-HIST1H2AG-3	chr6:26924772-26924962	NONHSAT108319
11	lnc-HIST1H2AG-3	chr6:26924771-26924962	ENSG00000224843.2
12	lnc-HIST1H2AG-3	chr6:26924879-26924962	XLOC_005216
13	lnc-HIST1H2AG-3	chr6:26924772-26924962	NONHSAT108320
14	lnc-HIST1H2BJ-10	chr6:26924168-26924285	NONHSAT108318

No data

Variant related genes	Relation type
GUSBP2	TF binding region
LINC00240	TF binding region
GUSBP2	CpG island
LINC00240	CpG island
ENSG00000238621	chromatin interactions
ENSG00000224843	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000241549	chromatin interactions

Extended variants
information (count: 853 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:853 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4634448	chr6:26911653-26911654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144419540	chr6:26911791-26911792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183722185	chr6:26911885-26911886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576125795	chr6:26911886-26911887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189111856	chr6:26912005-26912006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542515832	chr6:26912022-26912023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562247649	chr6:26912028-26912029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527846041	chr6:26912040-26912041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541305288	chr6:26912111-26912112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564603122	chr6:26912120-26912121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4351253	chr6:26912135-26912136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564808484	chr6:26912210-26912211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114321449	chr6:26912231-26912232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569687129	chr6:26912250-26912251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4351255	chr6:26912307-26912308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4278004	chr6:26912325-26912326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529252467	chr6:26912421-26912422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202133022	chr6:26912499-26912500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184189939	chr6:26914219-26914220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188178142	chr6:26914245-26914246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542989761	chr6:26914394-26914395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559456009	chr6:26914415-26914416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs180974875	chr6:26914420-26914421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6917814	chr6:26914425-26914426	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs564384141	chr6:26914554-26914555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565233123	chr6:26914567-26914568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10946881	chr6:26914611-26914612	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs7755054	chr6:26914643-26914644	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs569747893	chr6:26914684-26914685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12182270	chr6:26914697-26914698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372625927	chr6:26918945-26918946	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs560806587	chr6:26918958-26918959	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs532750037	chr6:26919054-26919055	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs7763149	chr6:26919078-26919079	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184024193	chr6:26919082-26919083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs141453011	chr6:26919117-26919118	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs548412926	chr6:26919144-26919145	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs568394013	chr6:26919197-26919198	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200798332	chr6:26919203-26919204	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs188194380	chr6:26919208-26919209	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs192756659	chr6:26919353-26919354	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs552840810	chr6:26919359-26919360	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs572850934	chr6:26919364-26919365	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs12191522	chr6:26919366-26919367	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs184449880	chr6:26919400-26919401	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs575113165	chr6:26919428-26919429	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs544267792	chr6:26919441-26919442	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs6905284	chr6:26919450-26919451	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs563042022	chr6:26919926-26919927	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs371659921	chr6:26919945-26919946	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	21569311	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26911600-26912600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:26914200-26914800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:26922000-26923000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:26922800-26923000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:26922800-26923000	Enhancers	K562	blood
6	chr6:26923000-26923800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:26923000-26924000	Weak transcription	K562	blood
8	chr6:26923400-26925400	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr6:26923800-26924000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr6:26923800-26924400	Active TSS	GM12878-XiMat	blood
11	chr6:26923800-26925000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:26923800-26925000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:26923800-26925000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr6:26923800-26925000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:26923800-26925000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:26923800-26925000	Active TSS	Left Ventricle	heart
17	chr6:26923800-26925000	Active TSS	HUVEC	blood vessel
18	chr6:26923800-26925200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr6:26923800-26925200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:26923800-26925200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:26923800-26925400	Active TSS	H1 Cell Line	embryonic stem cell
22	chr6:26923800-26925400	Active TSS	H9 Cell Line	embryonic stem cell
23	chr6:26923800-26925400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:26923800-26925400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:26923800-26925400	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr6:26923800-26925400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr6:26923800-26925400	Active TSS	Brain Anterior Caudate	brain
28	chr6:26923800-26925400	Active TSS	Brain Cingulate Gyrus	brain
29	chr6:26923800-26925400	Active TSS	Right Ventricle	heart
30	chr6:26923800-26925400	Active TSS	Stomach Smooth Muscle	stomach
31	chr6:26923800-26925400	Active TSS	NHDF-Ad	bronchial
32	chr6:26923800-26925600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:26923800-26925600	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr6:26923800-26925600	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr6:26923800-26925600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:26923800-26925600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr6:26923800-26925600	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr6:26923800-26925600	Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr6:26923800-26925600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:26923800-26925600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr6:26923800-26925600	Active TSS	Brain Angular Gyrus	brain
42	chr6:26923800-26925600	Active TSS	Duodenum Mucosa	Duodenum
43	chr6:26923800-26925600	Active TSS	Fetal Intestine Large	intestine
44	chr6:26923800-26925600	Active TSS	Fetal Intestine Small	intestine
45	chr6:26923800-26925600	Active TSS	Fetal Kidney	kidney
46	chr6:26923800-26925600	Active TSS	Pancreas	Pancrea
47	chr6:26923800-26925600	Active TSS	Rectal Mucosa Donor 29	rectum
48	chr6:26923800-26925600	Active TSS	Rectal Smooth Muscle	rectum
49	chr6:26923800-26925600	Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr6:26923800-26926000	Active TSS	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links