Variant report

Variant	nsv981326
Chromosome Location	chr6:44201100-44205684
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

No data

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:44123357..44125146-chr6:44203946..44206894,2	K562	blood:
2	chr6:44120961..44123352-chr6:44203847..44206405,2	MCF-7	breast:
3	chr3:139276752..139277509-chr6:44205350..44205852,2	MCF-7	breast:
4	chr6:44079762..44081284-chr6:44204790..44206941,2	K562	blood:
5	chr6:44067509..44068101-chr6:44205599..44206209,2	MCF-7	breast:
6	chr6:44117895..44119429-chr6:44199152..44201920,2	K562	blood:
7	chr6:44064502..44065068-chr6:44205526..44206089,2	MCF-7	breast:
8	chr6:44139023..44142178-chr6:44202710..44207835,5	K562	blood:
9	chr6:44140149..44141154-chr6:44205370..44206308,6	MCF-7	breast:
10	chr6:44051124..44053637-chr6:44204273..44206013,2	MCF-7	breast:
11	chr6:44052482..44055153-chr6:44202831..44205817,2	K562	blood:
12	chr6:44140545..44141089-chr6:44205316..44206164,2	MCF-7	breast:
13	chr6:44096398..44099100-chr6:44201010..44203822,2	K562	blood:
14	chr6:44093264..44095446-chr6:44204345..44207044,2	K562	blood:
15	chr6:44119282..44120002-chr6:44201581..44202498,4	MCF-7	breast:
16	chr6:44140078..44141155-chr6:44205142..44206527,19	K562	blood:
17	chr6:44201525..44202167-chr6:44213593..44214155,2	K562	blood:
18	chr6:44137717..44140173-chr6:44201270..44205583,3	MCF-7	breast:
19	chr6:44077806..44078726-chr6:44204971..44206412,4	MCF-7	breast:
20	chr6:44140559..44141134-chr6:44201407..44202489,4	MCF-7	breast:
21	chr6:44188965..44189915-chr6:44201606..44202486,3	MCF-7	breast:
22	chr6:44184911..44192138-chr6:44201380..44207306,8	MCF-7	breast:
23	chr6:44194591..44197466-chr6:44204314..44205838,2	MCF-7	breast:
24	chr6:43772379..43773030-chr6:44205542..44206258,2	MCF-7	breast:
25	chr6:44094095..44096990-chr6:44204419..44207697,4	MCF-7	breast:
26	chr6:44064173..44065096-chr6:44201605..44202510,3	K562	blood:
27	chr6:44199025..44201599-chr6:44203689..44206993,5	MCF-7	breast:
28	chr6:44064308..44065554-chr6:44205339..44206301,3	MCF-7	breast:
29	chr6:44196319..44199893-chr6:44200846..44202701,4	MCF-7	breast:
30	chr6:44140799..44143611-chr6:44200264..44202558,3	MCF-7	breast:
31	chr6:44118511..44121325-chr6:44203702..44206845,3	K562	blood:
32	chr6:44118934..44120172-chr6:44201616..44202538,11	MCF-7	breast:
33	chr6:44191141..44192105-chr6:44205563..44206387,6	MCF-7	breast:
34	chr6:44193349..44195595-chr6:44198490..44203873,4	MCF-7	breast:
35	chr6:44139881..44141095-chr6:44201450..44203123,17	MCF-7	breast:
36	chr6:43737632..43739680-chr6:44205540..44207219,3	MCF-7	breast:
37	chr6:44188998..44189909-chr6:44204941..44206651,4	K562	blood:
38	chr6:44202199..44204856-chr6:44206389..44207933,2	MCF-7	breast:
39	chr6:44199025..44201599-chr6:44203689..44206993,5	MCF-7	breast:
40	chr6:44064123..44065127-chr6:44205409..44206132,3	K562	blood:
41	chr6:44077806..44078726-chr6:44204971..44206412,5	MCF-7	breast:
42	chr6:44066164..44066852-chr6:44201933..44202598,2	MCF-7	breast:
43	chr6:44205429..44206336-chr6:44213621..44215036,3	K562	blood:
44	chr6:44064262..44065098-chr6:44201682..44202313,3	MCF-7	breast:
45	chr6:44141577..44142131-chr6:44201600..44202532,2	K562	blood:
46	chr6:44140158..44141271-chr6:44201179..44202684,11	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC29A1-2	chr6:44204713-44208319	NONHSAT112955

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	SLC29A1	hsa-miR-124-3p	chr6:44201820-44201839
2	SLC29A1	hsa-miR-124-3p	chr6:44201785-44201804
3	SLC29A1	hsa-miR-124-3p	chr6:44201832-44201838

Variant related genes	Relation type
ENSG00000272114	chromatin interactions
ENSG00000137216	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000180992	chromatin interactions
ENSG00000112715	chromatin interactions
ENSG00000112759	chromatin interactions

Extended variants
information (count: 175 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:175 , 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	rs324152	chr6:44201112-44201113	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200215385	chr6:44201141-44201142	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs199774402	chr6:44201147-44201148	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs544881367	chr6:44201164-44201165	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376950556	chr6:44201181-44201182	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs74750454	chr6:44201182-44201183	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs371621321	chr6:44201201-44201202	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140338369	chr6:44201230-44201231	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs375753872	chr6:44201238-44201239	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370351994	chr6:44201252-44201253	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs8187637	chr6:44201311-44201312	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201301264	chr6:44201312-44201313	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369843834	chr6:44201316-44201317	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs528317649	chr6:44201351-44201352	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs546769025	chr6:44201386-44201387	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571306317	chr6:44201402-44201403	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532283884	chr6:44201436-44201437	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550425829	chr6:44201493-44201494	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568929212	chr6:44201535-44201536	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543538594	chr6:44201581-44201582	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557132527	chr6:44201588-44201589	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528640310	chr6:44201594-44201595	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs536221050	chr6:44201610-44201611	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs554798146	chr6:44201651-44201652	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145776583	chr6:44201702-44201703	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78098903	chr6:44201706-44201707	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs14623	chr6:44201707-44201708	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs576891489	chr6:44201710-44201711	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs112703920	chr6:44201712-44201713	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs3734703	chr6:44201734-44201735	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs1046309	chr6:44201761-44201762	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544943554	chr6:44201793-44201794	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
33	rs72548775	chr6:44201807-44201808	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs559105847	chr6:44201883-44201884	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs9394993	chr6:44201920-44201921	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs3734704	chr6:44201947-44201948	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs376790806	chr6:44201954-44201955	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs73733879	chr6:44201965-44201966	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542166009	chr6:44201976-44201977	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560864527	chr6:44201977-44201978	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528191906	chr6:44201986-44201987	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs79459183	chr6:44201996-44201997	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs111409313	chr6:44202006-44202007	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183806793	chr6:44202050-44202051	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371370326	chr6:44202082-44202083	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs531055026	chr6:44202306-44202307	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568792776	chr6:44202321-44202322	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530074935	chr6:44202322-44202323	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs548567818	chr6:44202332-44202333	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs6458375	chr6:44202352-44202353	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:99)

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
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
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
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	21569311	CNVD
Cancer	20164920	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:638 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44191600-44205000	Weak transcription	Small Intestine	intestine
2	chr6:44192200-44204800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr6:44192400-44201200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr6:44192400-44201400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:44192400-44205000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr6:44193200-44204800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr6:44194400-44202000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr6:44194600-44202000	Weak transcription	Primary B cells from cord blood	blood
9	chr6:44194800-44201600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:44194800-44202400	Weak transcription	Fetal Kidney	kidney
11	chr6:44195000-44202200	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr6:44195000-44202800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr6:44195200-44201400	Transcr. at gene 5' and 3'	Stomach Smooth Muscle	stomach
14	chr6:44195200-44201800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:44195200-44202200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
16	chr6:44195200-44202600	Strong transcription	Dnd41	blood
17	chr6:44195400-44201400	Weak transcription	Stomach Mucosa	stomach
18	chr6:44195400-44201600	Weak transcription	Fetal Lung	lung
19	chr6:44195400-44202200	Weak transcription	Brain Germinal Matrix	brain
20	chr6:44195600-44201600	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr6:44195600-44201800	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr6:44195600-44201800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:44195600-44202000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:44195600-44202000	Genic enhancers	Adipose Nuclei	Adipose
25	chr6:44195600-44202200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr6:44195600-44202600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:44195600-44203000	Strong transcription	H9 Cell Line	embryonic stem cell
28	chr6:44195800-44201200	Strong transcription	Fetal Intestine Small	intestine
29	chr6:44195800-44201400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:44195800-44201600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:44196000-44201400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr6:44196000-44201400	Strong transcription	K562	blood
33	chr6:44196200-44201400	Strong transcription	Gastric	stomach
34	chr6:44196200-44201600	Genic enhancers	Placenta	Placenta
35	chr6:44196200-44201600	Genic enhancers	Right Ventricle	heart
36	chr6:44196400-44201400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:44196400-44201600	Strong transcription	Lung	lung
38	chr6:44196800-44201200	Strong transcription	Aorta	Aorta
39	chr6:44196800-44201600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr6:44197000-44201400	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr6:44197200-44201200	Genic enhancers	Colon Smooth Muscle	Colon
42	chr6:44197200-44201400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr6:44197200-44201400	Weak transcription	NHDF-Ad	bronchial
44	chr6:44197400-44201400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
45	chr6:44197400-44201400	Strong transcription	HepG2	liver
46	chr6:44197600-44201200	Strong transcription	Esophagus	oesophagus
47	chr6:44197600-44201200	Genic enhancers	Rectal Smooth Muscle	rectum
48	chr6:44197600-44201400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:44198200-44201200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:44198200-44201400	Weak transcription	NHLF	lung

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