Variant report

Variant	nsv601229
Chromosome Location	chr6:29566842-29588146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:429)
CpG islands
(count:5067)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr6:29570349-29570666	GM12878	blood:	n/a	n/a
2	BCL3	chr6:29570384-29570708	GM12878	blood:	n/a	n/a
3	CEBPB	chr6:29570824-29571015	K562	blood:	n/a	n/a
4	CHD2	chr6:29567899-29568097	K562	blood:	n/a	n/a
5	CTCF	chr6:29585975-29586222	K562	blood:	n/a	n/a
6	CTCF	chr6:29585980-29586130	GM12867	blood:	n/a	n/a
7	CTCF	chr6:29586020-29586170	GM12868	blood:	n/a	n/a
8	CTCF	chr6:29586120-29586270	MCF-7	breast:	n/a	n/a
9	CTCF	chr6:29570880-29571030	HFF-Myc	foreskin:	n/a	n/a
10	CTCF	chr6:29570680-29570830	BJ	skin:	n/a	n/a
11	CTCF	chr6:29586041-29586150	GM10248	blood:	n/a	n/a
12	CTCF	chr6:29586084-29586107	Pancreas_OC	pancreas:	n/a	n/a
13	CTCF	chr6:29586000-29586150	GM12867	blood:	n/a	n/a
14	CTCF	chr6:29570800-29570950	GM12867	blood:	n/a	n/a
15	CTCF	chr6:29586101-29586118	GM20000	blood:	n/a	n/a
16	CTCF	chr6:29586060-29586210	HCT-116	colon:	n/a	n/a
17	CTCF	chr6:29585876-29586327	K562	blood:	n/a	n/a
18	CTCF	chr6:29570880-29571030	AG04449	skin:	n/a	n/a
19	CTCF	chr6:29585980-29586130	GM12868	blood:	n/a	n/a
20	CTCF	chr6:29585980-29586130	SAEC	small airway:	n/a	n/a
21	CTCF	chr6:29585856-29586279	K562	blood:	n/a	n/a
22	CTCF	chr6:29584329-29584354	LNCaP	prostate:	n/a	n/a
23	CTCF	chr6:29570920-29571070	GM06990	blood:	n/a	n/a
24	CTCF	chr6:29570851-29571053	GM19238	blood:	n/a	n/a
25	CTCF	chr6:29570830-29571035	HepG2	liver:	n/a	n/a
26	CTCF	chr6:29570821-29571037	HepG2	liver:	n/a	n/a
27	CTCF	chr6:29570860-29571010	NHEK	skin:	n/a	n/a
28	CTCF	chr6:29570840-29570990	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr6:29586020-29586170	BJ	skin:	n/a	n/a
30	CTCF	chr6:29586100-29586250	A549	lung:	n/a	n/a
31	CTCF	chr6:29586000-29586150	GM12878	blood:	n/a	n/a
32	CTCF	chr6:29586060-29586210	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr6:29570840-29570990	GM12870	blood:	n/a	n/a
34	CTCF	chr6:29585898-29586293	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr6:29586040-29586190	GM12878	blood:	n/a	n/a
36	CTCF	chr6:29570840-29570990	GM12865	blood:	n/a	n/a
37	CTCF	chr6:29585980-29586130	RPTEC	kidney:	n/a	n/a
38	CTCF	chr6:29586040-29586190	GM12872	blood:	n/a	n/a
39	CTCF	chr6:29586060-29586210	HRE	kidney:	n/a	n/a
40	CTCF	chr6:29570900-29571050	GM12864	blood:	n/a	n/a
41	CTCF	chr6:29570880-29571030	K562	blood:	n/a	n/a
42	CTCF	chr6:29586000-29586150	AG04449	skin:	n/a	n/a
43	CTCF	chr6:29570900-29571050	A549	lung:	n/a	n/a
44	CTCF	chr6:29570863-29571049	Gliobla	brain:	n/a	n/a
45	CTCF	chr6:29570860-29571010	GM12878	blood:	n/a	n/a
46	CTCF	chr6:29570800-29570950	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr6:29586020-29586170	GM12866	blood:	n/a	n/a
48	CTCF	chr6:29570900-29571050	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr6:29570703-29570752	GM20000	blood:	n/a	n/a
50	CTCF	chr6:29571000-29571150	A549	lung:	n/a	n/a

(count:5067 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29570507-29570557	Caco-2	colon:	n/a
2	chr6:29571429-29571479	A549	lung:	n/a
3	chr6:29580896-29580946	NHBE	bronchial:	n/a
4	chr6:29586923-29586973	GM19239	blood:	n/a
5	chr6:29570507-29570557	Caco-2	colon:	n/a
6	chr6:29571429-29571479	A549	lung:	n/a
7	chr6:29580896-29580946	NHBE	bronchial:	n/a
8	chr6:29586923-29586973	GM19239	blood:	n/a
9	chr6:29572346-29572396	HCM	heart:	n/a
10	chr6:29577348-29577398	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:29578191-29578241	PANC-1	pancreas:	n/a
12	chr6:29581439-29581489	AG04449	skin:	fetal
13	chr6:29571468-29571518	GM06990	blood:	n/a
14	chr6:29573253-29573303	SKMC	muscle:	n/a
15	chr6:29579306-29579356	MCF10A-Er-Src	breast:	n/a
16	chr6:29570008-29570058	HRCEpiC	kidney:	n/a
17	chr6:29577082-29577132	ECC-1	luminal epithelium:	n/a
18	chr6:29574918-29574968	NT2-D1	testis:	n/a
19	chr6:29581182-29581232	HCPEpiC	choroid plexus:	n/a
20	chr6:29578496-29578546	Caco-2	colon:	n/a
21	chr6:29575128-29575178	HUVEC	blood vessel:	n/a
22	chr6:29574810-29574860	ECC-1	luminal epithelium:	n/a
23	chr6:29578191-29578241	HCT-116	colon:	n/a
24	chr6:29587487-29587537	K562	blood:	n/a
25	chr6:29572219-29572269	HRPEpiC	eye:	n/a
26	chr6:29572333-29572383	PFSK-1	brain:	n/a
27	chr6:29570707-29570757	SK-N-SH_RA	brain:	n/a
28	chr6:29580340-29580390	HEK293	kidney:	embryo
29	chr6:29582192-29582242	HCF	heart:	n/a
30	chr6:29586025-29586075	NT2-D1	testis:	n/a
31	chr6:29577006-29577056	MCF10A-Er-Src	breast:	n/a
32	chr6:29571074-29571124	HRPEpiC	eye:	n/a
33	chr6:29572346-29572396	HCT-116	colon:	n/a
34	chr6:29571693-29571743	MCF10A-Er-Src	breast:	n/a
35	chr6:29571468-29571518	Caco-2	colon:	n/a
36	chr6:29581439-29581489	U87	brain:	n/a
37	chr6:29586025-29586075	SKMC	muscle:	n/a
38	chr6:29581439-29581489	NHBE	bronchial:	n/a
39	chr6:29573089-29573139	AG09319	gingival:	n/a
40	chr6:29581105-29581155	ECC-1	luminal epithelium:	n/a
41	chr6:29572373-29572423	HCPEpiC	choroid plexus:	n/a
42	chr6:29580347-29580397	ProgFib	skin:	n/a
43	chr6:29570707-29570757	HCPEpiC	choroid plexus:	n/a
44	chr6:29580360-29580410	CMK	blood:	n/a
45	chr6:29579306-29579356	MCF-7	breast:	n/a
46	chr6:29582672-29582722	HRPEpiC	eye:	n/a
47	chr6:29579306-29579356	SAEC	small airway:	n/a
48	chr6:29571363-29571413	HCM	heart:	n/a
49	chr6:29570507-29570557	HUVEC	blood vessel:	n/a
50	chr6:29585617-29585667	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:29574743..29577585-chr6:29585500..29587353,2	K562	blood:
2	chr6:29565212..29568130-chr6:29573289..29574813,2	K562	blood:
3	chr6:29566782..29572750-chr6:29592808..29598864,8	K562	blood:
4	chr6:29564159..29568485-chr6:29574849..29577852,3	K562	blood:
5	chr6:29562440..29564140-chr6:29565910..29567515,2	K562	blood:
6	chr6:29573160..29575251-chr6:29581192..29583536,2	K562	blood:
7	chr6:29577860..29580564-chr6:29584385..29586719,2	K562	blood:
8	chr6:29564159..29568485-chr6:29574849..29577852,4	K562	blood:
9	chr6:29585702..29586556-chr6:29620907..29621418,2	K562	blood:
10	chr6:29581672..29583351-chr6:29584179..29587675,3	K562	blood:
11	chr6:29564780..29575712-chr6:29592511..29597522,14	K562	blood:
12	chr6:29566358..29568865-chr6:29570413..29572313,3	K562	blood:
13	chr6:29564159..29568485-chr6:29574849..29577852,4	K562	blood:
14	chr6:29560551..29562485-chr6:29568243..29569755,2	K562	blood:
15	chr6:29587184..29588996-chr6:29625794..29627418,2	K562	blood:
16	chr6:29560060..29561694-chr6:29565009..29566876,2	K562	blood:
17	chr6:29571256..29575251-chr6:29575309..29583536,9	K562	blood:
18	chr6:29566358..29568865-chr6:29570413..29572313,3	K562	blood:
19	chr6:29567658..29569553-chr6:29570192..29572225,2	K562	blood:
20	chr6:29587588..29589297-chr6:29589819..29592777,2	MCF-7	breast:
21	chr6:29564159..29568485-chr6:29574849..29577852,3	K562	blood:
22	chr6:29571256..29575251-chr6:29575309..29583536,9	K562	blood:
23	chr6:29584016..29586304-chr6:29588506..29590464,2	MCF-7	breast:
24	chr6:29578000..29583607-chr6:29584816..29592316,14	K562	blood:
25	chr6:29581672..29583351-chr6:29584179..29587675,3	K562	blood:
26	chr6:29581580..29583607-chr6:29588626..29591025,2	K562	blood:
27	chr6:29574743..29577585-chr6:29585500..29587353,2	K562	blood:
28	chr6:29578000..29583607-chr6:29584816..29592316,14	K562	blood:
29	chr6:29584985..29587112-chr6:29604597..29606396,2	K562	blood:
30	chr6:29579403..29583874-chr6:29593619..29596165,4	K562	blood:
31	chr6:29567658..29569553-chr6:29570192..29572225,2	K562	blood:
32	chr6:29572757..29580903-chr6:29593317..29599166,10	K562	blood:
33	chr6:29578909..29580835-chr6:29582417..29583981,2	K562	blood:
34	chr6:29576473..29579282-chr6:29593372..29595835,2	K562	blood:

No data

Variant related genes	Relation type
GABBR1	TF binding region
GABBR1	CpG island
ENSG00000204655	chromatin interactions
ENSG00000204681	chromatin interactions

Extended variants
information (count: 675 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3025646	chr6:29566842-29566843	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576132151	chr6:29566843-29566844	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375744604	chr6:29566854-29566855	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184846301	chr6:29566908-29566909	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs575081123	chr6:29566983-29566984	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189203525	chr6:29567082-29567083	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560805880	chr6:29567140-29567141	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577491074	chr6:29567162-29567163	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557099407	chr6:29567217-29567218	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs116873390	chr6:29567294-29567295	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs180675848	chr6:29567298-29567299	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs28986306	chr6:29567315-29567316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs144625548	chr6:29567316-29567317	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs561851976	chr6:29567353-29567354	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs527445514	chr6:29567369-29567370	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547288463	chr6:29567452-29567453	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186499245	chr6:29567468-29567469	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs539328499	chr6:29567480-29567481	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550080739	chr6:29567499-29567500	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs564205452	chr6:29567502-29567503	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs569658369	chr6:29567538-29567539	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535489285	chr6:29567551-29567552	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189320853	chr6:29567595-29567596	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs376116774	chr6:29567598-29567599	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572179853	chr6:29567603-29567604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs3025645	chr6:29567621-29567622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs554052248	chr6:29567623-29567624	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs362518	chr6:29567638-29567639	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs546171104	chr6:29567651-29567652	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562894398	chr6:29567656-29567657	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575984484	chr6:29567659-29567660	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs114693417	chr6:29567665-29567666	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561815146	chr6:29567766-29567767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs28986307	chr6:29567786-29567787	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547896638	chr6:29567794-29567795	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs370094218	chr6:29567803-29567804	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139482537	chr6:29567847-29567848	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs533193709	chr6:29567861-29567862	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549803417	chr6:29567897-29567898	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569968186	chr6:29567898-29567899	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562630151	chr6:29567942-29567943	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556281172	chr6:29567993-29567994	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181870201	chr6:29568001-29568002	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs55642345	chr6:29568002-29568003	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533151887	chr6:29568061-29568062	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs28986308	chr6:29568068-29568069	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs113423987	chr6:29568072-29568073	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs62406584	chr6:29568082-29568083	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs186981147	chr6:29568162-29568163	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs74345739	chr6:29568192-29568193	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	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
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
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	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
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29546200-29569400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:29559400-29568400	Weak transcription	HMEC	breast
3	chr6:29561200-29567800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:29561400-29567200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:29561400-29567600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:29561600-29567600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:29561600-29567600	Weak transcription	Fetal Stomach	stomach
8	chr6:29561600-29569000	Weak transcription	Spleen	Spleen
9	chr6:29561600-29569400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr6:29561600-29569600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr6:29561600-29569800	Weak transcription	Fetal Muscle Trunk	muscle
12	chr6:29561600-29570000	Weak transcription	Brain Hippocampus Middle	brain
13	chr6:29561600-29570000	Weak transcription	Lung	lung
14	chr6:29561600-29570000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr6:29561600-29570200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:29561600-29570600	Weak transcription	Right Ventricle	heart
17	chr6:29561600-29571600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr6:29561800-29569400	Weak transcription	Fetal Lung	lung
19	chr6:29561800-29570200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:29561800-29571600	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr6:29561800-29573200	Weak transcription	HSMMtube	muscle
22	chr6:29562000-29567800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr6:29562000-29568400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr6:29562000-29569200	Weak transcription	Brain Anterior Caudate	brain
25	chr6:29562000-29569400	Weak transcription	Fetal Muscle Leg	muscle
26	chr6:29562000-29569800	Weak transcription	K562	blood
27	chr6:29562000-29570600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:29562000-29571800	Weak transcription	Left Ventricle	heart
29	chr6:29562000-29572600	Weak transcription	Fetal Heart	heart
30	chr6:29563000-29567400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:29563000-29569000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:29563000-29569400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr6:29563400-29569000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:29564000-29569200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:29564000-29569600	Weak transcription	Fetal Brain Male	brain
36	chr6:29564400-29567600	Weak transcription	NH-A	brain
37	chr6:29564400-29569600	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr6:29564600-29567000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr6:29564600-29567200	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr6:29564600-29567200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr6:29564800-29567400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr6:29564800-29569200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr6:29565000-29567000	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr6:29565200-29568800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr6:29565200-29570200	Weak transcription	Fetal Kidney	kidney
46	chr6:29565400-29569400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:29565600-29570400	Weak transcription	NHDF-Ad	bronchial
48	chr6:29565600-29572200	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr6:29565800-29568400	Weak transcription	NHEK	skin
50	chr6:29565800-29569000	Weak transcription	Osteobl	bone

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