Variant report

Variant	nsv601487
Chromosome Location	chr6:30972589-30991559
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	chr6:30979120-30979201	HepG2	liver:	n/a	n/a
2	ATF2	chr6:30973365-30973754	GM12878	blood:	n/a	n/a
3	BATF	chr6:30973281-30973770	GM12878	blood:	n/a	n/a
4	BCL3	chr6:30973432-30973825	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:30979042-30979231	HepG2	liver:	n/a	n/a
6	BHLHE40	chr6:30973591-30973592	GM12878	blood:	n/a	n/a
7	CEBPB	chr6:30976622-30976873	HepG2	liver:	n/a	chr6:30976725-30976736
8	CEBPB	chr6:30976628-30976872	IMR90	lung:	n/a	chr6:30976725-30976736
9	CEBPB	chr6:30982027-30982185	IMR90	lung:	n/a	n/a
10	CEBPB	chr6:30976650-30976850	A549	lung:	n/a	chr6:30976725-30976736
11	CHD1	chr6:30978038-30978834	IMR90	lung:	n/a	n/a
12	CREB1	chr6:30973235-30973814	GM12878	blood:	n/a	n/a
13	CREB1	chr6:30972028-30972614	GM12878	blood:	n/a	n/a
14	CTCF	chr6:30976080-30976230	WERI-Rb-1	eye:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
15	CTCF	chr6:30976040-30976190	HAc	cerebellar:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
16	CTCF	chr6:30976141-30976177	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr6:30990801-30990847	LNCaP	prostate:	n/a	n/a
18	CTCF	chr6:30976080-30976230	HRE	kidney:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
19	CTCF	chr6:30976089-30976239	Gliobla	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
20	CTCF	chr6:30976080-30976230	SK-N-SH_RA	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
21	CTCF	chr6:30976118-30976228	SK-N-SH_RA	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
22	CTCF	chr6:30976010-30976305	H1-hESC	embryonic stem cell:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
23	CTCF	chr6:30976040-30976190	HCPEpiC	choroid plexus:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
24	CTCF	chr6:30976135-30976226	HepG2	liver:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
25	CTCF	chr6:30976017-30976266	SK-N-SH_RA	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
26	CTCF	chr6:30988289-30988331	Fibrobl	skin:	n/a	n/a
27	CTCF	chr6:30985540-30985690	GM12868	blood:	n/a	n/a
28	CTCF	chr6:30976140-30976290	SK-N-SH_RA	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
29	CTCF	chr6:30976111-30976176	A549	lung:	n/a	n/a
30	CTCF	chr6:30976140-30976290	K562	blood:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
31	CTCF	chr6:30976100-30976250	HPF	lung:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
32	CTCF	chr6:30976140-30976290	BE2_C	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
33	CTCF	chr6:30976100-30976250	HEK293	kidney:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
34	CTCF	chr6:30976120-30976270	BJ	skin:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
35	CTCF	chr6:30976085-30976234	K562	blood:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
36	CTCF	chr6:30976120-30976270	HepG2	liver:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
37	CTCF	chr6:30976120-30976270	BE2_C	brain:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
38	CTCF	chr6:30976100-30976250	AG09309	skin:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
39	CTCF	chr6:30976040-30976190	HRPEpiC	eye:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
40	CTCF	chr6:30976048-30976242	HepG2	liver:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
41	CTCF	chr6:30976040-30976190	HRE	kidney:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
42	CTCF	chr6:30976040-30976190	HVMF	connective:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
43	CTCF	chr6:30976120-30976270	HCPEpiC	choroid plexus:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
44	CTCF	chr6:30976096-30976237	H1-hESC	embryonic stem cell:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
45	CTCF	chr6:30976021-30976314	H1-hESC	embryonic stem cell:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
46	CTCF	chr6:30976140-30976290	A549	lung:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
47	CTCF	chr6:30975998-30976298	HepG2	liver:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
48	CTCF	chr6:30976133-30976140	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr6:30976060-30976210	HEEpiC	esophagus:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190
50	CTCF	chr6:30976060-30976210	AG10803	skin:	n/a	chr6:30976167-30976185 chr6:30976168-30976184 chr6:30976169-30976190

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30984791-30984841	AoSMC	blood vessel:	n/a
2	chr6:30988582-30988632	GM06990	blood:	n/a
3	chr6:30984791-30984841	AoSMC	blood vessel:	n/a
4	chr6:30988582-30988632	GM06990	blood:	n/a
5	chr6:30984791-30984841	HepG2	liver:	n/a
6	chr6:30988817-30988867	AG04450	lung:	fetal
7	chr6:30988817-30988867	Jurkat	blood:	n/a
8	chr6:30988694-30988744	NH-A	brain:	n/a
9	chr6:30988694-30988744	HMEC	breast:	n/a
10	chr6:30984668-30984718	MCF-7	breast:	n/a
11	chr6:30988694-30988744	MCF10A-Er-Src	breast:	n/a
12	chr6:30988582-30988632	NH-A	brain:	n/a
13	chr6:30984791-30984841	GM12878	blood:	n/a
14	chr6:30988817-30988867	HCT-116	colon:	n/a
15	chr6:30984668-30984718	SK-N-SH_RA	brain:	n/a
16	chr6:30981960-30982010	NH-A	brain:	n/a
17	chr6:30984668-30984718	HL-60	blood:	n/a
18	chr6:30980847-30980897	HUVEC	blood vessel:	n/a
19	chr6:30984791-30984841	SKMC	muscle:	n/a
20	chr6:30980847-30980897	ProgFib	skin:	n/a
21	chr6:30984791-30984841	H1-hESC	embryonic stem cell:	embryo
22	chr6:30984668-30984718	AoSMC	blood vessel:	n/a
23	chr6:30988694-30988744	MCF-7	breast:	n/a
24	chr6:30988582-30988632	T-47D	breast:	n/a
25	chr6:30988582-30988632	SKMC	muscle:	n/a
26	chr6:30988694-30988744	HRPEpiC	eye:	n/a
27	chr6:30980847-30980897	GM12892	blood:	n/a
28	chr6:30988694-30988744	GM12891	blood:	n/a
29	chr6:30984668-30984718	U87	brain:	n/a
30	chr6:30981960-30982010	SAEC	small airway:	n/a
31	chr6:30981960-30982010	HL-60	blood:	n/a
32	chr6:30984668-30984718	SK-N-MC	brain:	n/a
33	chr6:30980847-30980897	U87	brain:	n/a
34	chr6:30984791-30984841	SK-N-SH_RA	brain:	n/a
35	chr6:30988582-30988632	AG10803	skin:	n/a
36	chr6:30988582-30988632	AG04450	lung:	fetal
37	chr6:30984668-30984718	AG10803	skin:	n/a
38	chr6:30988817-30988867	Hela-S3	cervix:	n/a
39	chr6:30988694-30988744	HepG2	liver:	n/a
40	chr6:30980847-30980897	CMK	blood:	n/a
41	chr6:30984668-30984718	K562	blood:	n/a
42	chr6:30988817-30988867	SKMC	muscle:	n/a
43	chr6:30988582-30988632	MCF10A-Er-Src	breast:	n/a
44	chr6:30988582-30988632	GM12878	blood:	n/a
45	chr6:30988694-30988744	Jurkat	blood:	n/a
46	chr6:30984791-30984841	ECC-1	luminal epithelium:	n/a
47	chr6:30988582-30988632	HRE	kidney:	n/a
48	chr6:30988694-30988744	SK-N-SH_RA	brain:	n/a
49	chr6:30988817-30988867	LNCaP	prostate:	n/a
50	chr6:30988694-30988744	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:26026654..26028309-chr6:30981430..30984025,2	K562	blood:
2	chr6:30967966..30971967-chr6:30974378..30977539,3	K562	blood:
3	chr6:26157901..26159583-chr6:30975186..30977903,2	K562	blood:
4	chr6:30989389..30991180-chr6:30994181..30996114,2	K562	blood:
5	chr6:30966029..30968135-chr6:30974071..30975905,2	MCF-7	breast:
6	chr6:30975520..30978451-chr6:30989094..30991003,2	K562	blood:
7	chr6:30990191..30992901-chr6:31003159..31005249,2	K562	blood:
8	chr6:30954105..30955673-chr6:30975592..30977694,2	K562	blood:
9	chr6:30781714..30783791-chr6:30982862..30984438,2	K562	blood:
10	chr6:30971805..30974320-chr6:30984460..30987060,2	K562	blood:
11	chr6:30971805..30974320-chr6:30984460..30987060,2	K562	blood:
12	chr6:30976019..30976653-chr6:31010220..31010809,2	MCF-7	breast:

Variant related genes	Relation type
MUC22	TF binding region
MUC22	CpG island
ENSG00000261272	chromatin interactions
ENSG00000124529	chromatin interactions
ENSG00000158373	chromatin interactions

Extended variants
information (count: 1018 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:1018 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1634717	chr6:30972589-30972590	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144651996	chr6:30972599-30972600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182467678	chr6:30972743-30972744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371522511	chr6:30972823-30972824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139987643	chr6:30972837-30972838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1634718	chr6:30972865-30972866	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs574185092	chr6:30972895-30972896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143934997	chr6:30972941-30972942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199952175	chr6:30972953-30972954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374433970	chr6:30972959-30972960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs202210333	chr6:30972961-30972962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557094800	chr6:30973015-30973016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs59316452	chr6:30973017-30973018	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs9394024	chr6:30973088-30973089	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs189070174	chr6:30973108-30973109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200575727	chr6:30973133-30973134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs9368651	chr6:30973146-30973147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573236719	chr6:30973151-30973152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1634719	chr6:30973165-30973166	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs555748182	chr6:30973194-30973195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114914856	chr6:30973243-30973244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550830613	chr6:30973269-30973270	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs563064271	chr6:30973331-30973332	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs2523915	chr6:30973358-30973359	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs551611245	chr6:30973376-30973377	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs566833621	chr6:30973446-30973447	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2523916	chr6:30973519-30973520	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs1624944	chr6:30973535-30973536	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs140948123	chr6:30973624-30973625	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs535515711	chr6:30973633-30973634	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs373858	chr6:30973636-30973637	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs575352549	chr6:30973648-30973649	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs56111713	chr6:30973650-30973651	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs60192216	chr6:30973665-30973666	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs139386391	chr6:30973696-30973697	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs12110532	chr6:30973783-30973784	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12193866	chr6:30973843-30973844	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs140234453	chr6:30973863-30973864	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs544666425	chr6:30973879-30973880	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs560853084	chr6:30973922-30973923	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs145378967	chr6:30973929-30973930	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs551956680	chr6:30974041-30974042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551549676	chr6:30974049-30974050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560359681	chr6:30974050-30974051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527954544	chr6:30974078-30974079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111628690	chr6:30974104-30974105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146449813	chr6:30974206-30974207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568011676	chr6:30974232-30974233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs193022639	chr6:30974241-30974242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550613005	chr6:30974246-30974247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	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
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	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
Breast cancer	21785460	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30965200-30975800	Weak transcription	Gastric	stomach
2	chr6:30970600-30978000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:30971200-30974800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:30971600-30972800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr6:30972200-30972600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:30972200-30972600	Enhancers	Left Ventricle	heart
7	chr6:30972200-30972600	Enhancers	Lung	lung
8	chr6:30972200-30972600	Enhancers	Right Atrium	heart
9	chr6:30972200-30972600	Enhancers	Right Ventricle	heart
10	chr6:30972200-30972600	Enhancers	NHEK	skin
11	chr6:30972200-30973000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:30972200-30973200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:30972200-30973200	Enhancers	Small Intestine	intestine
14	chr6:30972200-30973400	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr6:30972200-30974000	Enhancers	GM12878-XiMat	blood
16	chr6:30972400-30972600	Enhancers	Psoas Muscle	Psoas
17	chr6:30972400-30972600	Enhancers	K562	blood
18	chr6:30972400-30973400	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr6:30972400-30973400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:30972400-30973400	Enhancers	Adipose Nuclei	Adipose
21	chr6:30972400-30973400	Enhancers	HMEC	breast
22	chr6:30972400-30973600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:30972400-30973800	Enhancers	Fetal Heart	heart
24	chr6:30972400-30974400	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr6:30972600-30972800	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr6:30972600-30972800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:30972600-30975000	Weak transcription	Left Ventricle	heart
28	chr6:30972600-30975200	Weak transcription	NHEK	skin
29	chr6:30972600-30975400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:30972600-30997600	Weak transcription	Right Atrium	heart
31	chr6:30973200-30973400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:30973200-30975000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:30973400-30975000	Weak transcription	HMEC	breast
34	chr6:30973400-30976000	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr6:30973600-30975600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:30974000-30976200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:30974400-30975200	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr6:30975000-30975200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:30975000-30975200	Enhancers	Left Ventricle	heart
40	chr6:30975000-30976000	Enhancers	NHLF	lung
41	chr6:30975000-30976200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr6:30975000-30976200	Enhancers	HSMMtube	muscle
43	chr6:30975000-30976200	Enhancers	NH-A	brain
44	chr6:30975000-30976400	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr6:30975000-30976400	Enhancers	Placenta Amnion	Placenta Amnion
46	chr6:30975000-30976400	Enhancers	HMEC	breast
47	chr6:30975000-30976400	Enhancers	HSMM	muscle
48	chr6:30975000-30976400	Enhancers	NHDF-Ad	bronchial
49	chr6:30975000-30979400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:30975200-30975400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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