Variant report

Variant	nsv884473
Chromosome Location	chr6:31815779-31827045
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:34)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31758879..31760783-chr6:31824444..31826875,2	K562	blood:
2	chr6:31632018..31634069-chr6:31823995..31825857,2	K562	blood:
3	chr6:31803990..31806815-chr6:31815888..31817775,2	MCF-7	breast:
4	chr6:31800580..31812447-chr6:31823435..31837480,47	K562	blood:
5	chr6:31795632..31798160-chr6:31824691..31826752,2	K562	blood:
6	chr6:31815422..31817421-chr6:31818452..31821417,3	K562	blood:
7	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
8	chr6:31812462..31817546-chr6:31826667..31830345,6	K562	blood:
9	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
10	chr6:31824043..31826980-chr6:31834536..31836163,2	MCF-7	breast:
11	chr6:31815431..31818520-chr6:31828570..31831003,3	K562	blood:
12	chr6:31820892..31822757-chr6:31826752..31828343,2	K562	blood:
13	chr6:31808421..31810311-chr6:31817022..31818530,2	MCF-7	breast:
14	chr6:31812462..31817546-chr6:31826667..31830345,6	K562	blood:
15	chr6:31818673..31820811-chr6:31829187..31833018,3	K562	blood:
16	chr6:31694918..31699964-chr6:31826467..31832957,9	K562	blood:
17	chr6:31813210..31815471-chr6:31820927..31823318,2	MCF-7	breast:
18	chr6:31819196..31821598-chr6:31823233..31824787,2	K562	blood:
19	chr6:31704564..31706667-chr6:31825357..31827075,2	K562	blood:
20	chr6:31815422..31817421-chr6:31818452..31821417,3	K562	blood:
21	chr6:31817673..31819263-chr6:31821738..31824406,2	MCF-7	breast:
22	chr6:31631387..31634828-chr6:31824744..31828511,4	K562	blood:
23	chr6:31801090..31813654-chr6:31824519..31834411,41	MCF-7	breast:
24	chr6:31812540..31817762-chr6:31828557..31832875,6	MCF-7	breast:
25	chr6:31512787..31515537-chr6:31826894..31829379,2	MCF-7	breast:
26	chr6:31819388..31820980-chr6:31829059..31830636,2	MCF-7	breast:
27	chr6:31820892..31822757-chr6:31826752..31828343,2	K562	blood:
28	chr6:31821795..31823838-chr6:31828365..31830760,3	MCF-7	breast:
29	chr6:31617566..31622844-chr6:31826455..31835211,65	K562	blood:
30	chr6:31811833..31815343-chr6:31817409..31821248,7	K562	blood:
31	chr6:31810854..31812545-chr6:31814196..31816031,2	MCF-7	breast:
32	chr6:31788461..31791125-chr6:31825621..31827331,2	K562	blood:
33	chr6:31817673..31819263-chr6:31821738..31824406,2	MCF-7	breast:
34	chr6:31819196..31821598-chr6:31823233..31824787,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf48-1	chr6:31825327-31825541	expReg_chr6_3066_+

No data

Variant related genes	Relation type
ENSG00000254870	chromatin interactions
ENSG00000227198	chromatin interactions
ENSG00000213760	chromatin interactions
ENSG00000201823	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000204435	chromatin interactions
ENSG00000204394	chromatin interactions
ENSG00000263020	chromatin interactions
ENSG00000201754	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000213719	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000204387	chromatin interactions
ENSG00000204439	chromatin interactions
ENSG00000204385	chromatin interactions
ENSG00000204498	chromatin interactions
ENSG00000204438	chromatin interactions
ENSG00000204463	chromatin interactions

Extended variants
information (count: 379 )
Associated
traits (count: 133 )

Variant overlapped rSNPs/rCNVs (count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55705749	chr6:31815779-31815780	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs5875334	chr6:31815785-31815786	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs544041345	chr6:31815805-31815806	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567214091	chr6:31815808-31815809	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs550032934	chr6:31815873-31815874	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs184217676	chr6:31815904-31815905	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs116510468	chr6:31815905-31815906	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs376406073	chr6:31816049-31816050	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs530829862	chr6:31816050-31816051	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs28732162	chr6:31816059-31816060	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs565892869	chr6:31816068-31816069	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs536689207	chr6:31816078-31816079	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs554963799	chr6:31816136-31816137	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs576359840	chr6:31816180-31816181	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs537234805	chr6:31816343-31816344	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs558695140	chr6:31816413-31816414	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs577046052	chr6:31816416-31816417	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs371458786	chr6:31816443-31816444	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs577342421	chr6:31816461-31816462	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs188966214	chr6:31816466-31816467	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs571938252	chr6:31816489-31816490	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs561150317	chr6:31816645-31816646	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs531601558	chr6:31816663-31816664	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs181722851	chr6:31816711-31816712	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs550120226	chr6:31816712-31816713	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs565022972	chr6:31816790-31816791	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs532341950	chr6:31816792-31816793	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs184689919	chr6:31816812-31816813	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs190789983	chr6:31816814-31816815	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs145156836	chr6:31816840-31816841	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs536773453	chr6:31816889-31816890	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs58338320	chr6:31816901-31816902	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs370221610	chr6:31816909-31816910	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs540818637	chr6:31816920-31816921	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs137907851	chr6:31816935-31816936	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs562406433	chr6:31816967-31816968	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs552243035	chr6:31817049-31817050	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs544642824	chr6:31817078-31817079	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs28895017	chr6:31817114-31817115	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs547853569	chr6:31817129-31817130	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs537321477	chr6:31817175-31817176	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs558828790	chr6:31817217-31817218	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs576984513	chr6:31817219-31817220	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs180793140	chr6:31817227-31817228	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs74756639	chr6:31817233-31817234	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs186180760	chr6:31817241-31817242	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs148223575	chr6:31817252-31817253	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs560838523	chr6:31817260-31817261	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs368724664	chr6:31817271-31817272	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs543697738	chr6:31817295-31817296	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:133)

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
Lung cancer	18438408	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
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
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
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
Renal cell carcinoma	18765545	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
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	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
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31803000-31817200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:31807000-31829200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr6:31807400-31824800	Weak transcription	Brain Angular Gyrus	brain
4	chr6:31807400-31829400	Weak transcription	Fetal Brain Male	brain
5	chr6:31807400-31829600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr6:31807800-31825000	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:31807800-31826600	Weak transcription	Right Ventricle	heart
8	chr6:31807800-31827800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr6:31808000-31826600	Weak transcription	Fetal Kidney	kidney
10	chr6:31808000-31827000	Weak transcription	Small Intestine	intestine
11	chr6:31808000-31829400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr6:31808000-31829400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr6:31808000-31829800	Weak transcription	Psoas Muscle	Psoas
14	chr6:31808200-31826800	Weak transcription	NHDF-Ad	bronchial
15	chr6:31808600-31819000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr6:31808600-31823000	Weak transcription	Brain Cingulate Gyrus	brain
17	chr6:31808600-31825000	Weak transcription	Brain Anterior Caudate	brain
18	chr6:31808600-31825000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr6:31808600-31825200	Weak transcription	Aorta	Aorta
20	chr6:31808600-31826600	Weak transcription	Dnd41	blood
21	chr6:31808600-31827000	Weak transcription	NHEK	skin
22	chr6:31808600-31827600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:31808800-31816600	Weak transcription	GM12878-XiMat	blood
24	chr6:31808800-31819200	Weak transcription	A549	lung
25	chr6:31808800-31819200	Weak transcription	NH-A	brain
26	chr6:31808800-31819600	Weak transcription	Gastric	stomach
27	chr6:31808800-31820600	Weak transcription	Colon Smooth Muscle	Colon
28	chr6:31808800-31823200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:31808800-31824800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr6:31808800-31824800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr6:31808800-31824800	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr6:31808800-31825000	Weak transcription	Brain Substantia Nigra	brain
33	chr6:31808800-31825000	Weak transcription	HSMMtube	muscle
34	chr6:31808800-31825200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:31808800-31825200	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr6:31808800-31825400	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr6:31808800-31826600	Weak transcription	Primary B cells from cord blood	blood
38	chr6:31808800-31826600	Weak transcription	Rectal Smooth Muscle	rectum
39	chr6:31808800-31827200	Weak transcription	HMEC	breast
40	chr6:31808800-31827200	Weak transcription	HSMM	muscle
41	chr6:31808800-31829600	Weak transcription	HUVEC	blood vessel
42	chr6:31809000-31819000	Weak transcription	Liver	Liver
43	chr6:31809000-31819200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr6:31809000-31823000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr6:31809000-31824600	Weak transcription	Placenta	Placenta
46	chr6:31809000-31824600	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr6:31809000-31824800	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr6:31809000-31824800	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr6:31809000-31825000	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr6:31809000-31825000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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