Variant report

Variant	esv2322180
Chromosome Location	chr6:28764675-28780578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:635)
CpG islands
(count:672)
Chromatin interactive
region (count:32)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:635 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:28779758-28780087	K562	blood:	n/a	n/a
2	ARID3A	chr6:28777726-28777887	K562	blood:	n/a	n/a
3	ARID3A	chr6:28770404-28770887	K562	blood:	n/a	n/a
4	ARID3A	chr6:28775492-28775915	K562	blood:	n/a	n/a
5	ARID3A	chr6:28770461-28770741	HepG2	liver:	n/a	n/a
6	ATF1	chr6:28777822-28778148	K562	blood:	n/a	n/a
7	ATF1	chr6:28778534-28778777	K562	blood:	n/a	n/a
8	ATF1	chr6:28775513-28775854	K562	blood:	n/a	n/a
9	ATF1	chr6:28770452-28770723	K562	blood:	n/a	n/a
10	ATF1	chr6:28771747-28771919	K562	blood:	n/a	n/a
11	ATF2	chr6:28775485-28775878	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr6:28775382-28775972	HCT-116	colon:	n/a	n/a
13	ATF3	chr6:28779571-28780204	A549	lung:	n/a	n/a
14	ATF3	chr6:28770191-28770826	K562	blood:	n/a	n/a
15	ATF3	chr6:28775486-28775995	HCT-116	colon:	n/a	n/a
16	ATF3	chr6:28770153-28770948	A549	lung:	n/a	n/a
17	ATF3	chr6:28770324-28770803	HCT-116	colon:	n/a	n/a
18	ATF3	chr6:28779489-28780170	A549	lung:	n/a	n/a
19	ATF3	chr6:28770240-28770785	HCT-116	colon:	n/a	n/a
20	ATF3	chr6:28770218-28770915	A549	lung:	n/a	n/a
21	ATF3	chr6:28775351-28776014	K562	blood:	n/a	n/a
22	ATF3	chr6:28779602-28780245	HCT-116	colon:	n/a	n/a
23	ATF3	chr6:28775354-28776109	A549	lung:	n/a	n/a
24	ATF3	chr6:28779511-28780188	K562	blood:	n/a	n/a
25	ATF3	chr6:28775377-28775970	A549	lung:	n/a	n/a
26	ATF3	chr6:28779590-28780184	HCT-116	colon:	n/a	n/a
27	BACH1	chr6:28779802-28780088	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr6:28775490-28775810	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:28770522-28770819	GM12878	blood:	n/a	chr6:28770688-28770697
30	BDP1	chr6:28770461-28770892	K562	blood:	n/a	n/a
31	BDP1	chr6:28779761-28780193	K562	blood:	n/a	n/a
32	BDP1	chr6:28775505-28775933	Hela-S3	cervix:	n/a	n/a
33	BDP1	chr6:28770463-28770856	Hela-S3	cervix:	n/a	n/a
34	BDP1	chr6:28775501-28775941	K562	blood:	n/a	n/a
35	BDP1	chr6:28779740-28780143	Hela-S3	cervix:	n/a	n/a
36	BHLHE40	chr6:28777770-28778045	K562	blood:	n/a	n/a
37	BHLHE40	chr6:28779772-28780047	K562	blood:	n/a	n/a
38	BHLHE40	chr6:28770487-28770671	HepG2	liver:	n/a	n/a
39	BRCA1	chr6:28779794-28780006	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr6:28775529-28775782	H1-hESC	embryonic stem cell:	n/a	chr6:28775765-28775772
41	BRCA1	chr6:28779716-28779981	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr6:28775528-28775859	Hela-S3	cervix:	n/a	chr6:28775765-28775772
43	BRCA1	chr6:28770480-28770733	Hela-S3	cervix:	n/a	n/a
44	BRF1	chr6:28775531-28775882	Hela-S3	cervix:	n/a	n/a
45	BRF1	chr6:28775524-28775880	K562	blood:	n/a	n/a
46	CBX3	chr6:28770177-28770805	K562	blood:	n/a	n/a
47	CBX3	chr6:28777052-28777582	K562	blood:	n/a	n/a
48	CBX3	chr6:28779571-28780163	K562	blood:	n/a	n/a
49	CBX3	chr6:28770168-28770951	K562	blood:	n/a	n/a
50	CBX3	chr6:28775385-28775942	HCT-116	colon:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:28778226-28778276	Hela-S3	cervix:	n/a
2	chr6:28778226-28778276	Hela-S3	cervix:	n/a
3	chr6:28778121-28778171	GM06990	blood:	n/a
4	chr6:28778382-28778432	HNPCEpiC	eye:	n/a
5	chr6:28778091-28778141	HL-60	blood:	n/a
6	chr6:28778091-28778141	LNCaP	prostate:	n/a
7	chr6:28778195-28778245	NH-A	brain:	n/a
8	chr6:28778582-28778632	GM06990	blood:	n/a
9	chr6:28778121-28778171	NHDF-neo	bronchial:	n/a
10	chr6:28778382-28778432	Caco-2	colon:	n/a
11	chr6:28778676-28778726	HRPEpiC	eye:	n/a
12	chr6:28770593-28770643	U87	brain:	n/a
13	chr6:28778091-28778141	GM12878	blood:	n/a
14	chr6:28778382-28778432	NHDF-neo	bronchial:	n/a
15	chr6:28778121-28778171	IMR90	lung:	fetal
16	chr6:28778195-28778245	SK-N-SH_RA	brain:	n/a
17	chr6:28778676-28778726	AG09309	skin:	n/a
18	chr6:28778226-28778276	LNCaP	prostate:	n/a
19	chr6:28778676-28778726	GM12891	blood:	n/a
20	chr6:28778091-28778141	SK-N-SH	brain:	n/a
21	chr6:28778676-28778726	HEK293	kidney:	embryo
22	chr6:28770593-28770643	CMK	blood:	n/a
23	chr6:28778124-28778174	HepG2	liver:	n/a
24	chr6:28778124-28778174	SK-N-SH_RA	brain:	n/a
25	chr6:28770593-28770643	NB4	blood:	n/a
26	chr6:28770593-28770643	HCF	heart:	n/a
27	chr6:28778226-28778276	GM12891	blood:	n/a
28	chr6:28778582-28778632	BJ	skin:	n/a
29	chr6:28778226-28778276	Hepatocyte	liver:	n/a
30	chr6:28778121-28778171	Jurkat	blood:	n/a
31	chr6:28778091-28778141	HIPEpiC	eye:	n/a
32	chr6:28778676-28778726	HepG2	liver:	n/a
33	chr6:28770593-28770643	Hepatocyte	liver:	n/a
34	chr6:28778124-28778174	H1-hESC	embryonic stem cell:	embryo
35	chr6:28778582-28778632	NHDF-neo	bronchial:	n/a
36	chr6:28778382-28778432	Hepatocyte	liver:	n/a
37	chr6:28778382-28778432	K562	blood:	n/a
38	chr6:28778121-28778171	K562	blood:	n/a
39	chr6:28778676-28778726	AG04450	lung:	fetal
40	chr6:28778091-28778141	BJ	skin:	n/a
41	chr6:28770593-28770643	HMEC	breast:	n/a
42	chr6:28778124-28778174	HCM	heart:	n/a
43	chr6:28778195-28778245	T-47D	breast:	n/a
44	chr6:28770593-28770643	SK-N-MC	brain:	n/a
45	chr6:28778676-28778726	SKMC	muscle:	n/a
46	chr6:28778226-28778276	AG04450	lung:	fetal
47	chr6:28770593-28770643	MCF10A-Er-Src	breast:	n/a
48	chr6:28778226-28778276	HIPEpiC	eye:	n/a
49	chr6:28778392-28778442	HCT-116	colon:	n/a
50	chr6:28778382-28778432	AG09309	skin:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:28723125..28726078-chr6:28775767..28777359,2	K562	blood:
2	chr6:28746343..28748629-chr6:28776362..28778668,2	K562	blood:
3	chr6:28739213..28740105-chr6:28777494..28778016,2	K562	blood:
4	chr6:28760359..28764219-chr6:28771578..28776179,5	K562	blood:
5	chr6:28756573..28759569-chr6:28769791..28772080,4	K562	blood:
6	chr6:28771451..28773263-chr6:28777101..28779175,2	K562	blood:
7	chr6:28767356..28769263-chr6:28782865..28784537,2	K562	blood:
8	chr6:28770558..28773254-chr6:28806737..28808772,2	K562	blood:
9	chr6:28687938..28689790-chr6:28777726..28779382,2	K562	blood:
10	chr6:28761012..28764011-chr6:28768099..28770643,2	K562	blood:
11	chr6:28771451..28773263-chr6:28777101..28779175,2	K562	blood:
12	chr6:28777118..28779341-chr6:28889220..28890745,2	MCF-7	breast:
13	chr6:28761080..28764011-chr6:28767880..28769599,2	K562	blood:
14	chr6:28774860..28778003-chr6:28805367..28807894,3	K562	blood:
15	chr6:28774872..28779186-chr6:28780865..28786550,9	K562	blood:
16	chr6:28775179..28778043-chr6:28889400..28891921,3	MCF-7	breast:
17	chr6:28772556..28774593-chr6:28785044..28786627,2	K562	blood:
18	chr6:28762168..28764957-chr6:28971752..28974125,2	K562	blood:
19	chr6:28692413..28694711-chr6:28778373..28780345,2	K562	blood:
20	chr6:28769403..28772112-chr6:28910261..28912768,2	K562	blood:
21	chr6:28771461..28773672-chr6:28829844..28832711,2	K562	blood:
22	chr6:28757752..28760408-chr6:28765977..28767794,2	K562	blood:
23	chr6:28779162..28781130-chr6:28862892..28865549,2	K562	blood:
24	chr6:28769803..28772263-chr6:28862688..28865946,3	MCF-7	breast:
25	chr6:28760359..28762539-chr6:28774291..28776179,2	K562	blood:
26	chr6:28737526..28738316-chr6:28777463..28778342,2	K562	blood:
27	chr6:28768996..28771268-chr6:28774440..28778213,3	K562	blood:
28	chr6:28778307..28780155-chr6:28804697..28807128,2	K562	blood:
29	chr6:28723977..28727923-chr6:28779903..28783132,3	K562	blood:
30	chr6:28653637..28654159-chr6:28777644..28778612,2	MCF-7	breast:
31	chr6:28770520..28773672-chr6:28829844..28832870,3	K562	blood:
32	chr6:28768996..28771268-chr6:28774440..28778213,3	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM27-19	chr6:28770349-28770592	NONHSAT108485
2	lnc-TRIM27-18	chr6:28773744-28776603	NONHSAT108486

No data

Variant related genes	Relation type
ENSG00000265764	TF binding region
ENSG00000265764	CpG island
ENSG00000197935	chromatin interactions
ENSG00000265764	chromatin interactions
ENSG00000225173	chromatin interactions
ENSG00000225595	chromatin interactions
ENSG00000224157	chromatin interactions
ENSG00000204713	chromatin interactions
ENSG00000204709	chromatin interactions

Extended variants
information (count: 628 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567808593	chr6:28764684-28764685	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs530108525	chr6:28764793-28764794	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs28381660	chr6:28764817-28764818	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs532211579	chr6:28764821-28764822	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs57517815	chr6:28764904-28764905	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs57103404	chr6:28764907-28764908	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536429485	chr6:28764915-28764916	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs554608492	chr6:28764930-28764931	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs9257190	chr6:28764974-28764975	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs9468422	chr6:28764986-28764987	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs369588935	chr6:28764990-28764991	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs188493831	chr6:28765027-28765028	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs114847130	chr6:28765033-28765034	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs553702769	chr6:28765099-28765100	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs141539442	chr6:28765154-28765155	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs192883556	chr6:28765165-28765166	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs532923213	chr6:28765241-28765242	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs368746918	chr6:28765265-28765266	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs9257192	chr6:28765346-28765347	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs576301407	chr6:28765380-28765381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138361975	chr6:28765386-28765387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561344374	chr6:28765398-28765399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530189323	chr6:28765399-28765400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546793962	chr6:28765455-28765456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183177983	chr6:28765476-28765477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187853703	chr6:28765505-28765506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552829009	chr6:28765506-28765507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569247971	chr6:28765565-28765566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538031441	chr6:28765577-28765578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72850376	chr6:28765627-28765628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568340596	chr6:28765643-28765644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531909398	chr6:28765647-28765648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191262845	chr6:28765658-28765659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113742415	chr6:28765685-28765686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576725859	chr6:28765696-28765697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539108753	chr6:28765725-28765726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556489603	chr6:28765776-28765777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543205413	chr6:28765777-28765778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551556267	chr6:28765780-28765781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576440684	chr6:28765877-28765878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542165071	chr6:28765906-28765907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189351408	chr6:28765948-28765949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572278586	chr6:28765953-28765954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192601571	chr6:28765983-28765984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184466110	chr6:28765988-28765989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369528060	chr6:28766013-28766014	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs532525997	chr6:28766031-28766032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527370889	chr6:28766104-28766105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562818942	chr6:28766107-28766108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7454923	chr6:28766108-28766109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28763400-28764800	Active TSS	A549	lung
2	chr6:28763400-28770600	Weak transcription	HMEC	breast
3	chr6:28763600-28765000	Active TSS	K562	blood
4	chr6:28764200-28765400	Enhancers	HepG2	liver
5	chr6:28764600-28764800	Enhancers	Hela-S3	cervix
6	chr6:28764600-28770400	Weak transcription	GM12878-XiMat	blood
7	chr6:28765000-28769600	Weak transcription	K562	blood
8	chr6:28765400-28768400	Weak transcription	HepG2	liver
9	chr6:28768600-28768800	Enhancers	HepG2	liver
10	chr6:28768800-28769000	Enhancers	Placenta	Placenta
11	chr6:28769600-28770200	Enhancers	K562	blood
12	chr6:28770200-28770400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:28770200-28770400	Flanking Active TSS	K562	blood
14	chr6:28770200-28771600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
15	chr6:28770200-28771800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
16	chr6:28770200-28771800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
17	chr6:28770400-28770600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
18	chr6:28770400-28770600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr6:28770400-28770600	Flanking Bivalent TSS/Enh	HepG2	liver
20	chr6:28770400-28770800	Active TSS	Hela-S3	cervix
21	chr6:28770400-28771200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:28770400-28771400	Enhancers	GM12878-XiMat	blood
23	chr6:28770400-28771600	Active TSS	H9 Cell Line	embryonic stem cell
24	chr6:28770400-28771600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:28770400-28771600	Active TSS	K562	blood
26	chr6:28770400-28771800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
27	chr6:28770400-28771800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
28	chr6:28770400-28771800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
29	chr6:28770400-28771800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
30	chr6:28770400-28771800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
31	chr6:28770400-28771800	Active TSS	A549	lung
32	chr6:28770600-28770800	Bivalent/Poised TSS	HepG2	liver
33	chr6:28770600-28770800	Enhancers	HMEC	breast
34	chr6:28770600-28771000	Active TSS	NHEK	skin
35	chr6:28770600-28771200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr6:28770600-28771800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr6:28770800-28771000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr6:28770800-28771200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:28770800-28771200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:28770800-28771200	Active TSS	NHLF	lung
41	chr6:28770800-28771400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr6:28770800-28771400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
43	chr6:28770800-28771400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:28770800-28771400	Flanking Active TSS	HMEC	breast
45	chr6:28770800-28771600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
46	chr6:28770800-28771600	Flanking Bivalent TSS/Enh	HepG2	liver
47	chr6:28770800-28771800	Flanking Active TSS	Hela-S3	cervix
48	chr6:28771000-28771200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:28771000-28771200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr6:28771000-28771200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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