Variant report

Variant	esv3377596
Chromosome Location	chr6:34243274-34247372
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	ARID3A	chr6:34245066-34245563	K562	blood:	n/a	n/a
2	ATF1	chr6:34245133-34245466	K562	blood:	n/a	n/a
3	BHLHE40	chr6:34244803-34245502	K562	blood:	n/a	n/a
4	CCNT2	chr6:34245177-34245593	K562	blood:	n/a	n/a
5	CCNT2	chr6:34244474-34244971	K562	blood:	n/a	n/a
6	CCNT2	chr6:34246152-34246406	K562	blood:	n/a	n/a
7	CTCF	chr6:34245092-34245470	K562	blood:	n/a	n/a
8	CTCF	chr6:34244120-34244270	WERI-Rb-1	eye:	n/a	n/a
9	CUX1	chr6:34244487-34245599	K562	blood:	n/a	n/a
10	E2F4	chr6:34244672-34244733	MCF10A-Er-Src	breast:	n/a	n/a
11	ELF1	chr6:34243189-34243547	K562	blood:	n/a	n/a
12	EP300	chr6:34244979-34245569	K562	blood:	n/a	n/a
13	EP300	chr6:34245295-34245314	K562	blood:	n/a	n/a
14	GATA2	chr6:34244980-34245553	K562	blood:	n/a	chr6:34245329-34245339 chr6:34245328-34245344 chr6:34245332-34245341 chr6:34245332-34245339 chr6:34245325-34245346 chr6:34245332-34245339 chr6:34245331-34245341 chr6:34245332-34245339
15	HCFC1	chr6:34245396-34245596	K562	blood:	n/a	n/a
16	HMGN3	chr6:34245179-34245479	K562	blood:	n/a	n/a
17	HNF4A	chr6:34244533-34244987	HepG2	liver:	n/a	chr6:34244758-34244770 chr6:34244757-34244770 chr6:34244596-34244608 chr6:34244758-34244771 chr6:34244757-34244770 chr6:34244756-34244771
18	HNF4A	chr6:34244640-34244971	HepG2	liver:	n/a	chr6:34244758-34244770 chr6:34244757-34244770 chr6:34244758-34244771 chr6:34244757-34244770 chr6:34244756-34244771
19	IRF1	chr6:34245140-34245451	K562	blood:	n/a	n/a
20	JUND	chr6:34245139-34245539	K562	blood:	n/a	n/a
21	MAFF	chr6:34245243-34245599	K562	blood:	n/a	n/a
22	MAFK	chr6:34243264-34243464	HepG2	liver:	n/a	chr6:34243331-34243346
23	MAFK	chr6:34243248-34243447	HepG2	liver:	n/a	chr6:34243331-34243346
24	MAFK	chr6:34245147-34245447	K562	blood:	n/a	n/a
25	MAX	chr6:34245208-34245585	K562	blood:	n/a	chr6:34245404-34245413 chr6:34245409-34245417 chr6:34245406-34245416 chr6:34245406-34245415 chr6:34245406-34245415 chr6:34245406-34245415
26	MAX	chr6:34244487-34245090	K562	blood:	n/a	n/a
27	MAX	chr6:34245138-34245730	K562	blood:	n/a	chr6:34245404-34245413 chr6:34245409-34245417 chr6:34245406-34245416 chr6:34245406-34245415 chr6:34245406-34245415 chr6:34245406-34245415
28	MAX	chr6:34245241-34245565	K562	blood:	n/a	chr6:34245404-34245413 chr6:34245409-34245417 chr6:34245406-34245416 chr6:34245406-34245415 chr6:34245406-34245415 chr6:34245406-34245415
29	MAX	chr6:34244635-34245058	HepG2	liver:	n/a	n/a
30	MAZ	chr6:34245194-34245514	K562	blood:	n/a	chr6:34245404-34245413 chr6:34245409-34245417 chr6:34245406-34245416 chr6:34245406-34245415 chr6:34245406-34245415 chr6:34245406-34245415
31	MXI1	chr6:34244556-34245023	HepG2	liver:	n/a	chr6:34244787-34244796 chr6:34244646-34244655
32	MXI1	chr6:34245385-34245511	K562	blood:	n/a	chr6:34245405-34245414 chr6:34245407-34245416
33	MYBL2	chr6:34244476-34244968	HepG2	liver:	n/a	n/a
34	MYC	chr6:34245179-34245613	K562	blood:	n/a	chr6:34245404-34245413 chr6:34245409-34245417 chr6:34245406-34245416 chr6:34245406-34245415 chr6:34245406-34245415 chr6:34245406-34245415
35	MYC	chr6:34244733-34244842	HepG2	liver:	n/a	n/a
36	MYC	chr6:34245346-34245443	K562	blood:	n/a	chr6:34245404-34245413 chr6:34245409-34245417 chr6:34245406-34245416 chr6:34245406-34245415 chr6:34245406-34245415 chr6:34245406-34245415
37	MYC	chr6:34245321-34245322	K562	blood:	n/a	n/a
38	MYC	chr6:34244625-34245643	K562	blood:	n/a	chr6:34245404-34245413 chr6:34245409-34245417 chr6:34245406-34245416 chr6:34245406-34245415 chr6:34245406-34245415 chr6:34245406-34245415
39	NR3C1	chr6:34244780-34244952	A549	lung:	n/a	chr6:34244886-34244900 chr6:34244885-34244901 chr6:34244884-34244901
40	POLR2A	chr6:34246483-34246805	K562	blood:	n/a	n/a
41	POLR2A	chr6:34246869-34247563	K562	blood:	n/a	n/a
42	POLR2A	chr6:34245621-34245970	K562	blood:	n/a	n/a
43	POLR2A	chr6:34245077-34245614	K562	blood:	n/a	n/a
44	POLR2A	chr6:34246429-34246755	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr6:34246633-34247140	A549	lung:	n/a	n/a
46	POLR2A	chr6:34244580-34244595	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr6:34245751-34245903	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr6:34244769-34244952	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr6:34246943-34247197	H1-neurons	neurons:	n/a	n/a
50	POLR2A	chr6:34246568-34247365	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:34239719..34243509-chr6:34291067..34294837,5	K562	blood:
2	chr6:34242678..34244532-chr6:34357227..34359923,2	MCF-7	breast:
3	chr6:34241825..34244661-chr6:34360011..34362275,2	K562	blood:
4	chr6:34243359..34245671-chr6:34250933..34253670,2	MCF-7	breast:
5	chr6:34214507..34216888-chr6:34245546..34249056,4	K562	blood:
6	chr6:34232764..34235632-chr6:34243482..34245527,2	MCF-7	breast:
7	chr6:34239800..34242616-chr6:34243635..34245743,3	K562	blood:
8	chr6:34202426..34206348-chr6:34246132..34251181,8	K562	blood:
9	chr6:34243756..34245812-chr6:34390841..34393824,2	K562	blood:
10	chr6:34211942..34216855-chr6:34244859..34247946,7	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGA1-2	chr6:34246917-34254539	NONHSAT112121
2	lnc-HMGA1-2	chr6:34246917-34249243	NONHSAT112120

Variant related genes	Relation type
ENSG00000225339	TF binding region
ENSG00000137309	chromatin interactions
ENSG00000272325	chromatin interactions
ENSG00000186577	chromatin interactions
ENSG00000124614	chromatin interactions

Extended variants
information (count: 174 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:174 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527891543	chr6:34243285-34243286	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs547723097	chr6:34243288-34243289	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs567942147	chr6:34243304-34243305	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs548086252	chr6:34243325-34243326	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189290257	chr6:34243361-34243362	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs73420943	chr6:34243480-34243481	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs6916965	chr6:34243513-34243514	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs375681006	chr6:34243570-34243571	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs545877303	chr6:34243582-34243583	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs564570454	chr6:34243618-34243619	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371870692	chr6:34243620-34243621	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs35694679	chr6:34243641-34243642	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376503680	chr6:34243642-34243643	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs61360305	chr6:34243643-34243644	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs76457768	chr6:34243644-34243645	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374046555	chr6:34243649-34243650	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201850077	chr6:34243650-34243651	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201482952	chr6:34243651-34243652	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs79483637	chr6:34243652-34243653	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs63284760	chr6:34243654-34243655	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs370856522	chr6:34243655-34243656	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs60048079	chr6:34243669-34243670	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs150571363	chr6:34243703-34243704	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192882326	chr6:34243737-34243738	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200231007	chr6:34243753-34243754	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs373650932	chr6:34243772-34243773	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs111235205	chr6:34243783-34243784	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562255782	chr6:34243802-34243803	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs529606119	chr6:34243804-34243805	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201428799	chr6:34243808-34243809	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs386700060	chr6:34243814-34243815	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs201350254	chr6:34243815-34243816	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs199748669	chr6:34243816-34243817	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs200901561	chr6:34243817-34243818	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs550646181	chr6:34243851-34243852	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs10440840	chr6:34243887-34243888	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs539572030	chr6:34243893-34243894	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs140071624	chr6:34243899-34243900	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557835793	chr6:34243901-34243902	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs369574116	chr6:34243934-34243935	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs184320125	chr6:34243935-34243936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs536591885	chr6:34243941-34243942	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533750537	chr6:34243988-34243989	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs112945592	chr6:34243989-34243990	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs146816658	chr6:34243990-34243991	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs188686667	chr6:34243991-34243992	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs556970696	chr6:34244002-34244003	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs575252674	chr6:34244040-34244041	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs115245297	chr6:34244132-34244133	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs181463772	chr6:34244167-34244168	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34218200-34255000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr6:34228600-34247000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:34229000-34246800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:34231200-34246600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:34233000-34251800	Weak transcription	NHDF-Ad	bronchial
6	chr6:34233200-34245400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:34234200-34247600	Weak transcription	Brain Germinal Matrix	brain
8	chr6:34235800-34245600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:34237000-34246600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr6:34238400-34259400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:34239000-34247600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr6:34239200-34246000	Weak transcription	Brain Angular Gyrus	brain
13	chr6:34239600-34247000	Weak transcription	Fetal Brain Female	brain
14	chr6:34239800-34245400	Weak transcription	Fetal Stomach	stomach
15	chr6:34240000-34244800	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr6:34240000-34246200	Enhancers	Left Ventricle	heart
17	chr6:34240200-34245400	Weak transcription	Stomach Smooth Muscle	stomach
18	chr6:34240200-34249000	Weak transcription	NHLF	lung
19	chr6:34240200-34250200	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr6:34240200-34255200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:34240400-34249600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr6:34240400-34251800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:34240400-34255000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr6:34240400-34259800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr6:34240400-34259800	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr6:34240600-34246000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr6:34240600-34247200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr6:34240600-34250400	Weak transcription	Brain Substantia Nigra	brain
29	chr6:34240600-34269200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr6:34240800-34261000	Weak transcription	Fetal Kidney	kidney
31	chr6:34241000-34248600	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr6:34241200-34245600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:34241400-34245800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr6:34241400-34246600	Weak transcription	Fetal Intestine Small	intestine
35	chr6:34241400-34260000	Weak transcription	Esophagus	oesophagus
36	chr6:34241600-34244800	Weak transcription	Fetal Muscle Leg	muscle
37	chr6:34241600-34245400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:34241600-34245400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:34241600-34246600	Weak transcription	Dnd41	blood
40	chr6:34241600-34249600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr6:34241600-34250400	Weak transcription	Fetal Thymus	thymus
42	chr6:34241600-34252800	Weak transcription	Stomach Mucosa	stomach
43	chr6:34241800-34243400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr6:34241800-34244400	Weak transcription	Fetal Heart	heart
45	chr6:34241800-34244600	Weak transcription	Placenta	Placenta
46	chr6:34241800-34244600	Weak transcription	Pancreas	Pancrea
47	chr6:34241800-34244800	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr6:34241800-34245600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:34241800-34245600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr6:34241800-34246200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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