Variant report

Variant	nsv524941
Chromosome Location	chr6:35734051-35745655
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	ATF3	chr6:35744208-35744420	K562	blood:	n/a	n/a
2	ATF3	chr6:35744121-35744436	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr6:35744219-35744446	HepG2	liver:	n/a	n/a
4	BACH1	chr6:35744245-35744377	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr6:35744225-35744401	K562	blood:	n/a	n/a
6	CCNT2	chr6:35744354-35744493	K562	blood:	n/a	n/a
7	CEBPB	chr6:35736577-35736818	HepG2	liver:	n/a	chr6:35736669-35736680
8	CEBPB	chr6:35745475-35745815	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:35736627-35736820	K562	blood:	n/a	chr6:35736669-35736680
10	CEBPB	chr6:35745492-35745805	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:35736563-35736730	A549	lung:	n/a	chr6:35736669-35736680
12	CEBPB	chr6:35736599-35736738	IMR90	lung:	n/a	chr6:35736669-35736680
13	CEBPB	chr6:35735049-35735267	HepG2	liver:	n/a	chr6:35735162-35735173 chr6:35735160-35735171
14	CEBPB	chr6:35744378-35744394	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:35745487-35745803	K562	blood:	n/a	n/a
16	CTCF	chr6:35744580-35744730	HMEC	breast:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
17	CTCF	chr6:35744440-35744590	GM12871	blood:	n/a	n/a
18	CTCF	chr6:35744460-35744610	GM12867	blood:	n/a	n/a
19	CTCF	chr6:35744580-35744730	HCPEpiC	choroid plexus:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
20	CTCF	chr6:35744640-35744790	GM12871	blood:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
21	CTCF	chr6:35734700-35734850	GM06990	blood:	n/a	chr6:35734819-35734826
22	CTCF	chr6:35744520-35744670	AoAF	blood vessel:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
23	CTCF	chr6:35744580-35744730	HEK293	kidney:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
24	CTCF	chr6:35744600-35744750	SK-N-SH_RA	brain:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
25	CTCF	chr6:35744560-35744710	GM12870	blood:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
26	CTCF	chr6:35744600-35744750	GM12871	blood:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
27	CTCF	chr6:35744689-35744694	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr6:35744620-35744770	HepG2	liver:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
29	CTCF	chr6:35744340-35744490	GM12874	blood:	n/a	n/a
30	CTCF	chr6:35744600-35744750	GM12873	blood:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
31	CTCF	chr6:35744580-35744730	WERI-Rb-1	eye:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
32	CTCF	chr6:35744520-35744670	AG04449	skin:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
33	CTCF	chr6:35744560-35744710	GM12875	blood:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
34	CTCF	chr6:35744160-35744310	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr6:35744620-35744770	GM12866	blood:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
36	CTCF	chr6:35744560-35744710	HCT-116	colon:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
37	CTCF	chr6:35744560-35744710	GM12874	blood:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
38	CTCF	chr6:35744540-35744690	HBMEC	blood vessel:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
39	CTCF	chr6:35736093-35736122	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:35744540-35744690	SK-N-SH_RA	brain:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
41	CTCF	chr6:35744560-35744710	HUVEC	blood vessel:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
42	CTCF	chr6:35744507-35744521	GM13977	blood:	n/a	n/a
43	CTCF	chr6:35744520-35744670	GM12875	blood:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
44	CTCF	chr6:35744633-35744681	H1-hESC	embryonic stem cell:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
45	CTCF	chr6:35744620-35744770	HPAF	blood vessel:	n/a	chr6:35744648-35744666 chr6:35744654-35744663 chr6:35744643-35744664
46	CTCF	chr6:35734640-35734790	HMF	breast:	n/a	n/a
47	CTCF	chr6:35744680-35744830	BE2_C	brain:	n/a	n/a
48	E2F6	chr6:35744162-35744434	K562	blood:	n/a	chr6:35744243-35744250
49	E2F6	chr6:35743944-35745054	H1-hESC	embryonic stem cell:	n/a	chr6:35744243-35744250
50	E2F6	chr6:35744037-35744939	H1-hESC	embryonic stem cell:	n/a	chr6:35744243-35744250

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35744605-35744655	GM06990	blood:	n/a
2	chr6:35744230-35744280	GM12878	blood:	n/a
3	chr6:35744226-35744276	PrEC	prostate:	n/a
4	chr6:35737336-35737386	AG09319	gingival:	n/a
5	chr6:35743705-35743755	SKMC	muscle:	n/a
6	chr6:35744230-35744280	PFSK-1	brain:	n/a
7	chr6:35744230-35744280	HNPCEpiC	eye:	n/a
8	chr6:35743107-35743157	GM12891	blood:	n/a
9	chr6:35737336-35737386	NH-A	brain:	n/a
10	chr6:35744188-35744238	MCF10A-Er-Src	breast:	n/a
11	chr6:35743107-35743157	SAEC	small airway:	n/a
12	chr6:35744355-35744405	HL-60	blood:	n/a
13	chr6:35743705-35743755	HMEC	breast:	n/a
14	chr6:35744226-35744276	SAEC	small airway:	n/a
15	chr6:35744355-35744405	A549	lung:	n/a
16	chr6:35744230-35744280	HRE	kidney:	n/a
17	chr6:35741544-35741594	MCF10A-Er-Src	breast:	n/a
18	chr6:35744355-35744405	H1-hESC	embryonic stem cell:	embryo
19	chr6:35743107-35743157	RPTEC	kidney:	n/a
20	chr6:35743705-35743755	SK-N-SH	brain:	n/a
21	chr6:35744188-35744238	AoSMC	blood vessel:	n/a
22	chr6:35734095-35734145	MCF-7	breast:	n/a
23	chr6:35743705-35743755	MCF-7	breast:	n/a
24	chr6:35743107-35743157	CMK	blood:	n/a
25	chr6:35737336-35737386	Hela-S3	cervix:	n/a
26	chr6:35744605-35744655	AoSMC	blood vessel:	n/a
27	chr6:35744605-35744655	ProgFib	skin:	n/a
28	chr6:35741544-35741594	NB4	blood:	n/a
29	chr6:35741544-35741594	HMEC	breast:	n/a
30	chr6:35743705-35743755	HepG2	liver:	n/a
31	chr6:35744355-35744405	BE2_C	brain:	n/a
32	chr6:35744355-35744405	HCM	heart:	n/a
33	chr6:35737336-35737386	GM12878	blood:	n/a
34	chr6:35744230-35744280	Hela-S3	cervix:	n/a
35	chr6:35744230-35744280	AG09309	skin:	n/a
36	chr6:35743705-35743755	AG09309	skin:	n/a
37	chr6:35743705-35743755	PANC-1	pancreas:	n/a
38	chr6:35734095-35734145	HCT-116	colon:	n/a
39	chr6:35744230-35744280	BJ	skin:	n/a
40	chr6:35741544-35741594	MCF-7	breast:	n/a
41	chr6:35741544-35741594	PFSK-1	brain:	n/a
42	chr6:35744355-35744405	LNCaP	prostate:	n/a
43	chr6:35744226-35744276	CMK	blood:	n/a
44	chr6:35743705-35743755	HPAEpiC	pulmonary alveolar:	n/a
45	chr6:35744226-35744276	MCF-7	breast:	n/a
46	chr6:35734095-35734145	HNPCEpiC	eye:	n/a
47	chr6:35744605-35744655	ovcar-3	ovarian:	n/a
48	chr6:35734095-35734145	HepG2	liver:	n/a
49	chr6:35744605-35744655	Jurkat	blood:	n/a
50	chr6:35743107-35743157	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:35742984..35745597-chr6:35763979..35765844,2	MCF-7	breast:
2	chr6:35732876..35736019-chr6:35742978..35745750,3	MCF-7	breast:
3	chr6:35741595..35743750-chr6:35746332..35747980,2	K562	blood:
4	chr6:35744273..35746880-chr6:35754146..35757378,3	K562	blood:
5	chr6:35732876..35736019-chr6:35742978..35745750,3	MCF-7	breast:
6	chr6:35535585..35537526-chr6:35741367..35743409,2	K562	blood:
7	chr6:35743802..35745883-chr6:35771884..35774045,2	MCF-7	breast:
8	chr6:35745381..35747955-chr6:35762666..35765104,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf126-1	chr6:35744371-35744581	NR_104469
2	lnc-C6orf126-1	chr6:35744371-35744581	NONHSAT112192
3	lnc-C6orf126-1	chr6:35745236-35745358	NONHSAT112192
4	lnc-C6orf126-1	chr6:35744467-35744581	NONHSAT112193

Variant related genes	Relation type
CLPSL1	TF binding region
CLPSL2	TF binding region
CLPSL1	CpG island
CLPSL2	CpG island
ENSG00000137392	chromatin interactions
ENSG00000204140	chromatin interactions
ENSG00000196748	chromatin interactions
ENSG00000220734	chromatin interactions
ENSG00000197753	chromatin interactions

Extended variants
information (count: 458 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2817056	chr6:35734051-35734052	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112768511	chr6:35734060-35734061	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557165362	chr6:35734068-35734069	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375231420	chr6:35734077-35734078	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs2766567	chr6:35734094-35734095	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs546082628	chr6:35734100-35734101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147790311	chr6:35734124-35734125	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528138159	chr6:35734177-35734178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs141141946	chr6:35734196-35734197	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561853805	chr6:35734221-35734222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2766568	chr6:35734238-35734239	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs182371386	chr6:35734240-35734241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569865217	chr6:35734251-35734252	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs531118694	chr6:35734264-35734265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77858131	chr6:35734295-35734296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571053522	chr6:35734354-35734355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs398048441	chr6:35734372-35734373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs77214017	chr6:35734373-35734374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs78131116	chr6:35734375-35734376	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12173543	chr6:35734386-35734387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs71002602	chr6:35734390-35734391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374111226	chr6:35734391-35734392	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs376771332	chr6:35734398-35734399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370964055	chr6:35734403-35734404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs530539310	chr6:35734410-35734411	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376356371	chr6:35734413-35734414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201512558	chr6:35734417-35734418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs375928293	chr6:35734422-35734423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542758536	chr6:35734430-35734431	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs143149882	chr6:35734449-35734450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs562536378	chr6:35734470-35734471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs7745231	chr6:35734481-35734482	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs73729787	chr6:35734524-35734525	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546019865	chr6:35734541-35734542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558063382	chr6:35734582-35734583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573040832	chr6:35734587-35734588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs74827100	chr6:35734606-35734607	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs561495548	chr6:35734637-35734638	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs528956491	chr6:35734656-35734657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568165946	chr6:35734658-35734659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201677423	chr6:35734659-35734660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140814201	chr6:35734660-35734661	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs543860396	chr6:35734696-35734697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565303994	chr6:35734702-35734703	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs35662542	chr6:35734704-35734705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200105380	chr6:35734706-35734707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs561005145	chr6:35734720-35734721	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs531055812	chr6:35734722-35734723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376149594	chr6:35734757-35734758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138651938	chr6:35734775-35734776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
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
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
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
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
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
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35732400-35744200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:35732600-35736800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:35732600-35739000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr6:35733800-35738400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:35736000-35737800	Enhancers	Placenta	Placenta
6	chr6:35736800-35737200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:35737800-35738000	Weak transcription	Placenta	Placenta
8	chr6:35737800-35738000	Flanking Active TSS	K562	blood
9	chr6:35737800-35738400	Enhancers	GM12878-XiMat	blood
10	chr6:35737800-35740000	Enhancers	Primary B cells from peripheral blood	blood
11	chr6:35737800-35740200	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr6:35738000-35738200	Active TSS	K562	blood
13	chr6:35738000-35740000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:35738200-35739800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:35738400-35738600	Flanking Active TSS	GM12878-XiMat	blood
16	chr6:35738400-35739200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:35738400-35739400	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr6:35738400-35739600	Enhancers	Primary hematopoietic stem cells	blood
19	chr6:35738400-35740000	Enhancers	Primary B cells from cord blood	blood
20	chr6:35738600-35738800	Enhancers	GM12878-XiMat	blood
21	chr6:35738600-35739400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:35738800-35739000	Flanking Active TSS	GM12878-XiMat	blood
23	chr6:35739000-35739600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr6:35739000-35739600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr6:35739000-35739600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr6:35739000-35739600	Enhancers	GM12878-XiMat	blood
27	chr6:35739000-35740000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:35739200-35739400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr6:35739200-35739400	Enhancers	Placenta	Placenta
30	chr6:35739200-35739600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:35739400-35739600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr6:35739600-35744000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:35739600-35744200	Weak transcription	Primary hematopoietic stem cells	blood
34	chr6:35740000-35744000	Weak transcription	Primary B cells from peripheral blood	blood
35	chr6:35740000-35744200	Weak transcription	Primary B cells from cord blood	blood
36	chr6:35740200-35743400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr6:35741400-35741600	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:35743000-35744200	Weak transcription	Right Atrium	heart
39	chr6:35743400-35744000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr6:35743800-35744000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:35743800-35744200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:35743800-35744200	Bivalent Enhancer	Placenta	Placenta
43	chr6:35744000-35744200	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr6:35744000-35744200	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:35744000-35744200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
46	chr6:35744000-35744200	Enhancers	Primary B cells from peripheral blood	blood
47	chr6:35744000-35744200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr6:35744000-35744200	Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr6:35744000-35744200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:35744000-35744200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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