Variant report

Variant	esv3327563
Chromosome Location	chr6:34037574-34042372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:146)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:146 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:34040726-34040770	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr6:34038484-34039145	GM12878	blood:	n/a	chr6:34038681-34038689 chr6:34038672-34038681
3	BCL3	chr6:34038584-34039181	GM12878	blood:	n/a	chr6:34038681-34038689 chr6:34038672-34038681
4	BHLHE40	chr6:34039681-34039895	K562	blood:	n/a	n/a
5	CBX3	chr6:34038893-34041263	K562	blood:	n/a	n/a
6	CBX3	chr6:34039045-34041038	K562	blood:	n/a	n/a
7	CEBPB	chr6:34039938-34040191	HepG2	liver:	n/a	n/a
8	CTCF	chr6:34039620-34039770	GM12872	blood:	n/a	n/a
9	CTCF	chr6:34042120-34042270	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr6:34042071-34042573	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr6:34042196-34042292	HepG2	liver:	n/a	n/a
12	CTCF	chr6:34042240-34042390	GM12878	blood:	n/a	n/a
13	CTCF	chr6:34039590-34040336	GM19239	blood:	n/a	n/a
14	CTCF	chr6:34042160-34042310	Caco-2	colon:	n/a	n/a
15	CTCF	chr6:34039740-34039890	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr6:34042160-34042310	A549	lung:	n/a	n/a
17	CTCF	chr6:34042160-34042310	HCT-116	colon:	n/a	n/a
18	CTCF	chr6:34041992-34042613	K562	blood:	n/a	n/a
19	CTCF	chr6:34042200-34042364	GM12892	blood:	n/a	n/a
20	CTCF	chr6:34039720-34039870	HepG2	liver:	n/a	n/a
21	CTCF	chr6:34042197-34042387	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:34042040-34042190	GM06990	blood:	n/a	n/a
23	CTCF	chr6:34039840-34039990	GM12866	blood:	n/a	n/a
24	CTCF	chr6:34042200-34042350	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr6:34042160-34042310	HepG2	liver:	n/a	n/a
26	CTCF	chr6:34040760-34040910	GM12872	blood:	n/a	n/a
27	CTCF	chr6:34040757-34040813	Lung_OC	lung:	n/a	n/a
28	CTCF	chr6:34042140-34042290	HMF	breast:	n/a	n/a
29	CTCF	chr6:34040342-34041005	GM19239	blood:	n/a	n/a
30	CTCF	chr6:34038260-34038410	WERI-Rb-1	eye:	n/a	chr6:34038319-34038332 chr6:34038317-34038335
31	CTCF	chr6:34041025-34041142	GM19239	blood:	n/a	n/a
32	CTCF	chr6:34042200-34042350	GM12874	blood:	n/a	n/a
33	CTCF	chr6:34042120-34042270	NHEK	skin:	n/a	n/a
34	CTCF	chr6:34038285-34038365	GM12892	blood:	n/a	chr6:34038319-34038332 chr6:34038317-34038335
35	CTCF	chr6:34042231-34042347	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:34042126-34042331	HepG2	liver:	n/a	n/a
37	CTCF	chr6:34039640-34039790	NB4	blood:	n/a	n/a
38	CTCF	chr6:34042216-34042347	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:34042180-34042330	AG04449	skin:	n/a	n/a
40	CTCF	chr6:34042216-34042308	GM19240	blood:	n/a	n/a
41	CTCF	chr6:34042140-34042290	AG04449	skin:	n/a	n/a
42	CTCF	chr6:34038160-34038310	GM06990	blood:	n/a	n/a
43	CTCF	chr6:34042140-34042290	GM12872	blood:	n/a	n/a
44	CTCF	chr6:34042045-34042446	K562	blood:	n/a	n/a
45	CTCF	chr6:34042160-34042310	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr6:34042149-34042324	T-47D	breast:	n/a	n/a
47	CTCF	chr6:34042255-34042320	Fibrobl	skin:	n/a	n/a
48	CTCF	chr6:34042054-34042421	K562	blood:	n/a	n/a
49	CTCF	chr6:34042180-34042330	HCT-116	colon:	n/a	n/a
50	CTCF	chr6:34042180-34042330	SK-N-SH_RA	brain:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33674390..33676592-chr6:34040123..34042729,2	MCF-7	breast:
2	chr6:33679075..33679957-chr6:34037863..34038862,2	MCF-7	breast:
3	chr6:34040958..34043775-chr6:34088032..34089661,2	MCF-7	breast:
4	chr6:34023974..34026204-chr6:34036920..34039187,2	MCF-7	breast:
5	chr6:34040358..34042713-chr6:34043195..34044850,2	K562	blood:
6	chr6:34032376..34034708-chr6:34039734..34041335,2	K562	blood:
7	chr6:34042273..34043918-chr6:34048694..34051267,2	K562	blood:
8	chr6:34024875..34026613-chr6:34038654..34040465,2	K562	blood:
9	chr6:34041534..34045824-chr6:34046497..34049415,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000221779	TF binding region
ENSG00000137288	chromatin interactions
ENSG00000124493	chromatin interactions

Extended variants
information (count: 318 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73410900	chr6:34037583-34037584	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12525132	chr6:34037640-34037641	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530805392	chr6:34037735-34037736	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552300415	chr6:34037750-34037751	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs79697957	chr6:34037751-34037752	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112945445	chr6:34037752-34037753	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs547135962	chr6:34037754-34037755	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377142133	chr6:34037767-34037768	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568680544	chr6:34037791-34037792	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140155737	chr6:34037792-34037793	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs78860211	chr6:34037819-34037820	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs10947477	chr6:34037855-34037856	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539434969	chr6:34037861-34037862	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs114481205	chr6:34037898-34037899	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs572943726	chr6:34037915-34037916	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs533771245	chr6:34037916-34037917	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs143920983	chr6:34037958-34037959	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs573864075	chr6:34037963-34037964	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs146836095	chr6:34037968-34037969	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs79481322	chr6:34037993-34037994	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs575263902	chr6:34038016-34038017	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs375715455	chr6:34038026-34038027	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs191664821	chr6:34038028-34038029	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs80236590	chr6:34038029-34038030	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs528536427	chr6:34038039-34038040	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs75926210	chr6:34038049-34038050	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs562266917	chr6:34038065-34038066	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs183105816	chr6:34038160-34038161	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs140568695	chr6:34038187-34038188	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs2499686	chr6:34038212-34038213	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs539458834	chr6:34038227-34038228	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs370237087	chr6:34038241-34038242	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs150108208	chr6:34038274-34038275	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs566576862	chr6:34038305-34038306	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs533845445	chr6:34038322-34038323	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs145537807	chr6:34038346-34038347	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs372835468	chr6:34038362-34038363	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs116097854	chr6:34038376-34038377	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs148821266	chr6:34038399-34038400	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs111269156	chr6:34038409-34038410	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs552668990	chr6:34038428-34038429	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs116317769	chr6:34038442-34038443	Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs186400621	chr6:34038540-34038541	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs546677457	chr6:34038555-34038556	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs545813446	chr6:34038556-34038557	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs34256571	chr6:34038570-34038571	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs397887958	chr6:34038571-34038572	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs56367515	chr6:34038595-34038596	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs55890362	chr6:34038596-34038597	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs568421342	chr6:34038597-34038598	Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Urothelial carcinoma	21177765	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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34025000-34101800	Weak transcription	Right Atrium	heart
2	chr6:34025200-34039600	Weak transcription	Gastric	stomach
3	chr6:34027400-34066400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:34033800-34041400	Weak transcription	Fetal Brain Female	brain
5	chr6:34035800-34037800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:34036000-34039200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:34036400-34038000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:34036600-34044800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:34036800-34038000	Enhancers	Fetal Brain Male	brain
10	chr6:34037000-34037800	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr6:34037200-34038000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr6:34037600-34038000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:34037600-34038000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:34038000-34038800	Active TSS	Spleen	Spleen
15	chr6:34038000-34039000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:34038000-34039800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:34038000-34042400	Weak transcription	Fetal Heart	heart
18	chr6:34038200-34038800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:34038200-34039000	Weak transcription	Esophagus	oesophagus
20	chr6:34038400-34039200	Weak transcription	Pancreas	Pancrea
21	chr6:34038800-34039400	Weak transcription	Spleen	Spleen
22	chr6:34039000-34039800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:34039000-34040200	ZNF genes & repeats	Esophagus	oesophagus
24	chr6:34039000-34041000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:34039200-34039600	Active TSS	Fetal Lung	lung
26	chr6:34039200-34040400	Genic enhancers	Pancreas	Pancrea
27	chr6:34039200-34041000	ZNF genes & repeats	Fetal Kidney	kidney
28	chr6:34039200-34041200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:34039400-34039600	Genic enhancers	Spleen	Spleen
30	chr6:34039400-34041000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
31	chr6:34039600-34039800	Transcr. at gene 5' and 3'	Spleen	Spleen
32	chr6:34039600-34040400	ZNF genes & repeats	Fetal Lung	lung
33	chr6:34039600-34040800	ZNF genes & repeats	Gastric	stomach
34	chr6:34039800-34040000	Active TSS	Spleen	Spleen
35	chr6:34039800-34040800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr6:34040000-34040200	Genic enhancers	Spleen	Spleen
37	chr6:34040200-34041000	Enhancers	Spleen	Spleen
38	chr6:34040400-34040800	Active TSS	Fetal Lung	lung
39	chr6:34040400-34040800	Transcr. at gene 5' and 3'	Pancreas	Pancrea
40	chr6:34040600-34041000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:34040800-34041000	ZNF genes & repeats	Pancreas	Pancrea
42	chr6:34040800-34041400	Active TSS	Gastric	stomach
43	chr6:34041000-34041400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr6:34041000-34041600	Weak transcription	Spleen	Spleen
45	chr6:34041000-34041800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:34041000-34044800	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr6:34041200-34041400	Enhancers	Fetal Brain Male	brain
48	chr6:34041200-34042200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:34041400-34041600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:34041400-34041800	Enhancers	Fetal Brain Female	brain

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