Variant report

Variant	esv1808861
Chromosome Location	chr6:35752498-35767027
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:96)
CpG islands
(count:855)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:96 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr6:35760699-35760763	K562	blood:	n/a	n/a
2	BHLHE40	chr6:35765017-35765289	K562	blood:	n/a	n/a
3	BHLHE40	chr6:35758607-35758807	HepG2	liver:	n/a	n/a
4	CEBPB	chr6:35758405-35758921	A549	lung:	n/a	n/a
5	CEBPB	chr6:35758561-35758682	HepG2	liver:	n/a	n/a
6	CEBPB	chr6:35758455-35758789	K562	blood:	n/a	n/a
7	CEBPB	chr6:35758454-35758819	A549	lung:	n/a	n/a
8	CEBPB	chr6:35756271-35756457	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:35758461-35758817	K562	blood:	n/a	n/a
10	CEBPB	chr6:35758462-35758824	IMR90	lung:	n/a	n/a
11	CEBPB	chr6:35758444-35758768	MCF-7	breast:	n/a	n/a
12	CEBPB	chr6:35758463-35758813	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:35758467-35758814	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:35762562-35762885	K562	blood:	n/a	n/a
15	CEBPB	chr6:35758448-35758812	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr6:35756680-35756830	GM12873	blood:	n/a	chr6:35756799-35756809
17	CTCF	chr6:35756160-35756310	GM12865	blood:	n/a	n/a
18	CTCF	chr6:35755520-35755670	GM12875	blood:	n/a	n/a
19	CTCF	chr6:35765740-35765890	GM12864	blood:	n/a	n/a
20	CTCF	chr6:35754820-35754970	GM12867	blood:	n/a	n/a
21	CTCF	chr6:35766010-35766063	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr6:35754720-35754870	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr6:35754680-35754830	HMEC	breast:	n/a	n/a
24	CTCF	chr6:35754640-35754790	GM12865	blood:	n/a	n/a
25	CTCF	chr6:35754620-35754770	SAEC	small airway:	n/a	n/a
26	CTCF	chr6:35760300-35760450	AG04449	skin:	n/a	n/a
27	CTCF	chr6:35760640-35760790	GM12868	blood:	n/a	n/a
28	E2F4	chr6:35759420-35759424	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F6	chr6:35766372-35766946	H1-hESC	embryonic stem cell:	n/a	n/a
30	E2F6	chr6:35766297-35766870	H1-hESC	embryonic stem cell:	n/a	n/a
31	E2F6	chr6:35761091-35761480	H1-hESC	embryonic stem cell:	n/a	chr6:35761248-35761260
32	E2F6	chr6:35761154-35761630	H1-hESC	embryonic stem cell:	n/a	chr6:35761248-35761260
33	E2F6	chr6:35761233-35761368	K562	blood:	n/a	chr6:35761248-35761260
34	EGR1	chr6:35765030-35765252	K562	blood:	n/a	n/a
35	EGR1	chr6:35763349-35763621	K562	blood:	n/a	chr6:35763477-35763491 chr6:35763478-35763491 chr6:35763479-35763490 chr6:35763479-35763490 chr6:35763479-35763488
36	ELF1	chr6:35764865-35765253	GM12878	blood:	n/a	n/a
37	FOXA1	chr6:35764086-35764407	T-47D	breast:	n/a	n/a
38	FOXA1	chr6:35764145-35764400	T-47D	breast:	n/a	n/a
39	GTF2F1	chr6:35766681-35766722	H1-hESC	embryonic stem cell:	n/a	n/a
40	GTF2F1	chr6:35765022-35765053	H1-hESC	embryonic stem cell:	n/a	n/a
41	GTF2F1	chr6:35763645-35763723	K562	blood:	n/a	n/a
42	HMGN3	chr6:35754741-35754755	K562	blood:	n/a	n/a
43	HNF4A	chr6:35755377-35755745	HepG2	liver:	n/a	chr6:35755619-35755634 chr6:35755620-35755632 chr6:35755620-35755633 chr6:35755620-35755632 chr6:35755619-35755634 chr6:35755620-35755632 chr6:35755619-35755634 chr6:35755618-35755633 chr6:35755619-35755634
44	HNF4A	chr6:35755424-35755827	HepG2	liver:	n/a	chr6:35755619-35755634 chr6:35755620-35755632 chr6:35755620-35755633 chr6:35755620-35755632 chr6:35755619-35755634 chr6:35755620-35755632 chr6:35755619-35755634 chr6:35755618-35755633 chr6:35755619-35755634
45	JUN	chr6:35765331-35765335	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAFF	chr6:35756435-35756454	HepG2	liver:	n/a	n/a
47	MAFF	chr6:35758034-35758157	K562	blood:	n/a	n/a
48	MAFF	chr6:35762574-35762875	K562	blood:	n/a	chr6:35762725-35762739 chr6:35762719-35762737
49	MAFF	chr6:35762658-35762770	HepG2	liver:	n/a	chr6:35762725-35762739 chr6:35762719-35762737
50	MAFK	chr6:35758054-35758231	HepG2	liver:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35756942-35756992	HRCEpiC	kidney:	n/a
2	chr6:35756942-35756992	HRCEpiC	kidney:	n/a
3	chr6:35765215-35765265	H1-hESC	embryonic stem cell:	embryo
4	chr6:35755609-35755659	Caco-2	colon:	n/a
5	chr6:35765215-35765265	PANC-1	pancreas:	n/a
6	chr6:35756942-35756992	GM12891	blood:	n/a
7	chr6:35765093-35765143	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:35756942-35756992	HNPCEpiC	eye:	n/a
9	chr6:35764958-35765008	PFSK-1	brain:	n/a
10	chr6:35765176-35765226	HUVEC	blood vessel:	n/a
11	chr6:35765589-35765639	K562	blood:	n/a
12	chr6:35764958-35765008	AG04449	skin:	fetal
13	chr6:35764958-35765008	AoSMC	blood vessel:	n/a
14	chr6:35764958-35765008	HRE	kidney:	n/a
15	chr6:35754796-35754846	HRCEpiC	kidney:	n/a
16	chr6:35766051-35766101	PANC-1	pancreas:	n/a
17	chr6:35755609-35755659	MCF10A-Er-Src	breast:	n/a
18	chr6:35755609-35755659	SAEC	small airway:	n/a
19	chr6:35765093-35765143	LNCaP	prostate:	n/a
20	chr6:35765093-35765143	HepG2	liver:	n/a
21	chr6:35766021-35766071	HRE	kidney:	n/a
22	chr6:35765589-35765639	NH-A	brain:	n/a
23	chr6:35765176-35765226	NH-A	brain:	n/a
24	chr6:35754796-35754846	T-47D	breast:	n/a
25	chr6:35766021-35766071	SKMC	muscle:	n/a
26	chr6:35765176-35765226	NHDF-neo	bronchial:	n/a
27	chr6:35756942-35756992	K562	blood:	n/a
28	chr6:35765589-35765639	ProgFib	skin:	n/a
29	chr6:35765093-35765143	HRCEpiC	kidney:	n/a
30	chr6:35765215-35765265	NH-A	brain:	n/a
31	chr6:35766021-35766071	NH-A	brain:	n/a
32	chr6:35764958-35765008	ovcar-3	ovarian:	n/a
33	chr6:35754906-35754956	PANC-1	pancreas:	n/a
34	chr6:35756942-35756992	GM19239	blood:	n/a
35	chr6:35755609-35755659	HRPEpiC	eye:	n/a
36	chr6:35765093-35765143	AG04450	lung:	fetal
37	chr6:35765176-35765226	HCPEpiC	choroid plexus:	n/a
38	chr6:35762844-35762894	Caco-2	colon:	n/a
39	chr6:35765589-35765639	NHDF-neo	bronchial:	n/a
40	chr6:35765215-35765265	HCPEpiC	choroid plexus:	n/a
41	chr6:35764958-35765008	ProgFib	skin:	n/a
42	chr6:35754906-35754956	SK-N-MC	brain:	n/a
43	chr6:35765215-35765265	GM12891	blood:	n/a
44	chr6:35762844-35762894	NB4	blood:	n/a
45	chr6:35762844-35762894	IMR90	lung:	fetal
46	chr6:35754796-35754846	Hela-S3	cervix:	n/a
47	chr6:35765589-35765639	IMR90	lung:	fetal
48	chr6:35764958-35765008	HIPEpiC	eye:	n/a
49	chr6:35765589-35765639	T-47D	breast:	n/a
50	chr6:35764958-35765008	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr6:35435012..35436668-chr6:35752247..35755003,2	MCF-7	breast:
2	chr6:35753638..35758618-chr6:35762629..35767095,7	K562	blood:
3	chr6:35742984..35745597-chr6:35763979..35765844,2	MCF-7	breast:
4	chr6:35753638..35758618-chr6:35762629..35767095,7	K562	blood:
5	chr6:35762283..35764266-chr6:35764644..35767426,2	MCF-7	breast:
6	chr6:35760846..35763760-chr6:36163836..36166432,2	K562	blood:
7	chr6:35744273..35746880-chr6:35754146..35757378,3	K562	blood:
8	chr6:35762307..35765078-chr6:35772426..35774241,2	MCF-7	breast:
9	chr6:35753847..35759789-chr6:35762486..35768711,9	K562	blood:
10	chr6:35762091..35764853-chr6:35765476..35768100,2	MCF-7	breast:
11	chr6:35753847..35759789-chr6:35762486..35768711,9	K562	blood:
12	chr6:35747942..35750162-chr6:35760132..35762411,2	MCF-7	breast:
13	chr6:35762091..35764853-chr6:35765476..35768100,2	MCF-7	breast:
14	chr6:35760015..35761880-chr6:35763280..35765561,2	K562	blood:

No data

Variant related genes	Relation type
CLPS	TF binding region
CLPSL1	TF binding region
CLPS	CpG island
CLPSL1	CpG island
ENSG00000246982	chromatin interactions
ENSG00000137392	chromatin interactions
ENSG00000196748	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000096070	chromatin interactions
ENSG00000197753	chromatin interactions
ENSG00000204140	chromatin interactions

Extended variants
information (count: 790 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:790 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12110921	chr6:35752551-35752552	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs113433762	chr6:35752556-35752557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143870674	chr6:35752615-35752616	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs2766586	chr6:35752634-35752635	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs61041019	chr6:35752640-35752641	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs551876426	chr6:35752678-35752679	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556796262	chr6:35752709-35752710	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2817067	chr6:35752761-35752762	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2766587	chr6:35752767-35752768	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs565178700	chr6:35752791-35752792	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs9470094	chr6:35752792-35752793	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs111263535	chr6:35752862-35752863	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs541351219	chr6:35752888-35752889	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34500810	chr6:35752951-35752952	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs70975107	chr6:35752972-35752973	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559979673	chr6:35752986-35752987	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs13217100	chr6:35753012-35753013	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530053794	chr6:35753015-35753016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548537027	chr6:35753018-35753019	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2817068	chr6:35753080-35753081	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs536532199	chr6:35753104-35753105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552697171	chr6:35753163-35753164	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs570706354	chr6:35753176-35753177	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192699561	chr6:35753197-35753198	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2817069	chr6:35753205-35753206	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs568311325	chr6:35753206-35753207	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs535107324	chr6:35753214-35753215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs183213791	chr6:35753219-35753220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2766588	chr6:35753227-35753228	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs545539645	chr6:35753233-35753234	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs145194082	chr6:35753234-35753235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577054391	chr6:35753285-35753286	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147695118	chr6:35753302-35753303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs186783528	chr6:35753365-35753366	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs530374042	chr6:35753376-35753377	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540465190	chr6:35753447-35753448	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192236831	chr6:35753459-35753460	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142432819	chr6:35753484-35753485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs150204199	chr6:35753491-35753492	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564556050	chr6:35753493-35753494	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528311345	chr6:35753506-35753507	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs560077344	chr6:35753528-35753529	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs9470095	chr6:35753559-35753560	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535781500	chr6:35753586-35753587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370575168	chr6:35753640-35753641	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs374293265	chr6:35753656-35753657	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs550596545	chr6:35753690-35753691	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs568538882	chr6:35753692-35753693	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs376327782	chr6:35753720-35753721	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs74857524	chr6:35753723-35753724	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35746400-35755400	Weak transcription	Pancreas	Pancrea
2	chr6:35750400-35754200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:35750600-35754600	Weak transcription	HMEC	breast
4	chr6:35752800-35753000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:35753000-35754800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:35754000-35754400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
7	chr6:35754200-35754400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
8	chr6:35754200-35754600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
9	chr6:35754200-35755400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:35754400-35754600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
11	chr6:35754400-35754600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:35754400-35754600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr6:35754400-35754600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:35754400-35754600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
15	chr6:35754400-35754800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
16	chr6:35754400-35755000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
17	chr6:35754400-35755000	Bivalent Enhancer	Right Ventricle	heart
18	chr6:35754400-35755000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
19	chr6:35754400-35755200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr6:35754400-35756000	Bivalent Enhancer	Placenta	Placenta
21	chr6:35754600-35754800	Bivalent Enhancer	Primary B cells from cord blood	blood
22	chr6:35754600-35754800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:35754600-35754800	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
24	chr6:35754600-35754800	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr6:35754600-35754800	Bivalent Enhancer	Fetal Intestine Large	intestine
26	chr6:35754600-35754800	Flanking Bivalent TSS/Enh	Lung	lung
27	chr6:35754600-35754800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
28	chr6:35754600-35754800	Flanking Active TSS	HMEC	breast
29	chr6:35754600-35755000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
30	chr6:35754600-35755000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr6:35754600-35755000	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:35754600-35755000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:35754600-35755000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr6:35754600-35755000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr6:35754600-35755000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:35754600-35755000	Bivalent/Poised TSS	Colonic Mucosa	Colon
37	chr6:35754600-35755000	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
38	chr6:35754600-35755000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr6:35754600-35755000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr6:35754600-35755000	Bivalent Enhancer	Left Ventricle	heart
41	chr6:35754600-35755000	Bivalent Enhancer	Ovary	ovary
42	chr6:35754600-35755200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr6:35754600-35755200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:35754600-35755200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr6:35754600-35755200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:35754600-35755400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
47	chr6:35754600-35755600	Bivalent Enhancer	Liver	Liver
48	chr6:35754800-35755000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
49	chr6:35754800-35755000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr6:35754800-35755000	Bivalent Enhancer	Esophagus	oesophagus

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