Variant report

Variant	esv1807818
Chromosome Location	chr6:44266574-44275011
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	BACH1	chr6:44272504-44272906	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:44272679-44272803	K562	blood:	n/a	n/a
3	BHLHE40	chr6:44272574-44272859	K562	blood:	n/a	n/a
4	BHLHE40	chr6:44272596-44272717	GM12878	blood:	n/a	n/a
5	CBX3	chr6:44272496-44272994	K562	blood:	n/a	n/a
6	CCNT2	chr6:44272600-44272981	K562	blood:	n/a	n/a
7	CEBPB	chr6:44272543-44272839	K562	blood:	n/a	n/a
8	CHD2	chr6:44272557-44272794	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr6:44272666-44272847	K562	blood:	n/a	n/a
10	CTCF	chr6:44272620-44272770	HPAF	blood vessel:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
11	CTCF	chr6:44272288-44272912	MCF-7	breast:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
12	CTCF	chr6:44272400-44272423	NHEK	skin:	n/a	n/a
13	CTCF	chr6:44272620-44272770	GM12872	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
14	CTCF	chr6:44272620-44272770	HRE	kidney:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
15	CTCF	chr6:44272401-44272434	GM12892	blood:	n/a	n/a
16	CTCF	chr6:44272400-44272550	NHEK	skin:	n/a	n/a
17	CTCF	chr6:44272640-44272790	AG04450	lung:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
18	CTCF	chr6:44272620-44272770	HCM	heart:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
19	CTCF	chr6:44272600-44272750	HRPEpiC	eye:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
20	CTCF	chr6:44272484-44272900	MCF-7	breast:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
21	CTCF	chr6:44272600-44272750	HUVEC	blood vessel:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
22	CTCF	chr6:44273300-44273450	GM06990	blood:	n/a	n/a
23	CTCF	chr6:44272574-44272805	MCF-7	breast:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
24	CTCF	chr6:44273040-44273190	WERI-Rb-1	eye:	n/a	chr6:44273153-44273162
25	CTCF	chr6:44272640-44272790	A549	lung:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
26	CTCF	chr6:44272300-44273002	SK-N-SH	brain:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
27	CTCF	chr6:44272558-44272859	GM12878	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
28	CTCF	chr6:44272580-44272730	GM12870	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
29	CTCF	chr6:44272910-44272916	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr6:44272620-44272770	GM12864	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
31	CTCF	chr6:44272640-44272790	RPTEC	kidney:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
32	CTCF	chr6:44271876-44271912	GM13977	blood:	n/a	n/a
33	CTCF	chr6:44272640-44272790	BJ	skin:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
34	CTCF	chr6:44272620-44272770	HEEpiC	esophagus:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
35	CTCF	chr6:44272508-44272875	GM12892	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
36	CTCF	chr6:44272620-44272770	GM12875	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
37	CTCF	chr6:44272538-44272840	GM19240	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
38	CTCF	chr6:44272389-44272444	GM19239	blood:	n/a	n/a
39	CTCF	chr6:44272620-44272770	SAEC	small airway:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
40	CTCF	chr6:44272487-44272869	SK-N-SH_RA	brain:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
41	CTCF	chr6:44272532-44272836	ProgFib	skin:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
42	CTCF	chr6:44272620-44272770	GM12868	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
43	CTCF	chr6:44272600-44272750	HAc	cerebellar:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
44	CTCF	chr6:44272640-44272790	GM12871	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
45	CTCF	chr6:44272549-44272825	MCF-7	breast:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
46	CTCF	chr6:44272355-44272933	K562	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
47	CTCF	chr6:44272923-44272984	Lung_OC	lung:	n/a	n/a
48	CTCF	chr6:44272600-44272750	AG04449	skin:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
49	CTCF	chr6:44272640-44272790	GM12864	blood:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690
50	CTCF	chr6:44272640-44272790	HCT-116	colon:	n/a	chr6:44272667-44272688 chr6:44272678-44272687 chr6:44272640-44272653 chr6:44272672-44272690

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:44268274-44268324	NT2-D1	testis:	n/a
2	chr6:44268274-44268324	AG09319	gingival:	n/a
3	chr6:44268274-44268324	HepG2	liver:	n/a
4	chr6:44268274-44268324	Hepatocyte	liver:	n/a
5	chr6:44268274-44268324	GM12891	blood:	n/a
6	chr6:44268274-44268324	Jurkat	blood:	n/a
7	chr6:44268274-44268324	HL-60	blood:	n/a
8	chr6:44268274-44268324	GM12878	blood:	n/a
9	chr6:44268274-44268324	HAEpiC	amniotic membrane:	n/a
10	chr6:44268274-44268324	NHDF-neo	bronchial:	n/a
11	chr6:44268274-44268324	AG09309	skin:	n/a
12	chr6:44268274-44268324	HIPEpiC	eye:	n/a
13	chr6:44268274-44268324	LNCaP	prostate:	n/a
14	chr6:44268274-44268324	SK-N-MC	brain:	n/a
15	chr6:44268274-44268324	SKMC	muscle:	n/a
16	chr6:44268274-44268324	HEEpiC	esophagus:	n/a
17	chr6:44268274-44268324	HRCEpiC	kidney:	n/a
18	chr6:44268274-44268324	CMK	blood:	n/a
19	chr6:44268274-44268324	HCPEpiC	choroid plexus:	n/a
20	chr6:44268274-44268324	Hela-S3	cervix:	n/a
21	chr6:44268274-44268324	ovcar-3	ovarian:	n/a
22	chr6:44268274-44268324	MCF10A-Er-Src	breast:	n/a
23	chr6:44268274-44268324	MCF-7	breast:	n/a
24	chr6:44268274-44268324	SK-N-SH_RA	brain:	n/a
25	chr6:44268274-44268324	IMR90	lung:	fetal
26	chr6:44268274-44268324	AoSMC	blood vessel:	n/a
27	chr6:44268274-44268324	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:44268274-44268324	BE2_C	brain:	n/a
29	chr6:44268274-44268324	HNPCEpiC	eye:	n/a
30	chr6:44268274-44268324	T-47D	breast:	n/a
31	chr6:44268274-44268324	HCT-116	colon:	n/a
32	chr6:44268274-44268324	HMEC	breast:	n/a
33	chr6:44268274-44268324	AG04450	lung:	fetal
34	chr6:44268274-44268324	U87	brain:	n/a
35	chr6:44268274-44268324	HCM	heart:	n/a
36	chr6:44268274-44268324	HCF	heart:	n/a
37	chr6:44268274-44268324	A549	lung:	n/a
38	chr6:44268274-44268324	HEK293	kidney:	embryo
39	chr6:44268274-44268324	RPTEC	kidney:	n/a
40	chr6:44268274-44268324	H1-hESC	embryonic stem cell:	embryo
41	chr6:44268274-44268324	NB4	blood:	n/a
42	chr6:44268274-44268324	PFSK-1	brain:	n/a
43	chr6:44268274-44268324	GM19239	blood:	n/a
44	chr6:44268274-44268324	HRPEpiC	eye:	n/a
45	chr6:44268274-44268324	ECC-1	luminal epithelium:	n/a
46	chr6:44268274-44268324	SK-N-SH	brain:	n/a
47	chr6:44268274-44268324	PANC-1	pancreas:	n/a
48	chr6:44268274-44268324	NHBE	bronchial:	n/a
49	chr6:44268274-44268324	AG10803	skin:	n/a
50	chr6:44268274-44268324	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:44063516..44066397-chr6:44271609..44273554,2	K562	blood:
2	chr6:44232053..44233854-chr6:44274858..44277076,2	MCF-7	breast:
3	chr11:62606512..62609356-chr6:44264959..44266812,2	MCF-7	breast:
4	chr6:44252510..44254427-chr6:44270655..44272831,2	MCF-7	breast:
5	chr6:44221494..44225979-chr6:44269650..44274771,6	K562	blood:
6	chr6:44235757..44236368-chr6:44272215..44272871,2	K562	blood:
7	chr6:44214688..44216634-chr6:44271584..44273822,2	K562	blood:
8	chr6:44235432..44236394-chr6:44272155..44273117,4	MCF-7	breast:
9	chr6:44235750..44236849-chr6:44272248..44273140,3	MCF-7	breast:
10	chr6:44272619..44273140-chr6:44281766..44282700,2	K562	blood:
11	chr6:44213299..44216188-chr6:44269950..44273084,4	K562	blood:
12	chr6:44237771..44241790-chr6:44264717..44266725,3	MCF-7	breast:
13	chr6:44216083..44217678-chr6:44271012..44273836,2	MCF-7	breast:
14	chr6:44250404..44254517-chr6:44264090..44267267,4	MCF-7	breast:
15	chr6:44231713..44233466-chr6:44264708..44267385,2	MCF-7	breast:
16	chr6:44223584..44225235-chr6:44274881..44277464,2	MCF-7	breast:
17	chr6:44223567..44227779-chr6:44264321..44266816,4	MCF-7	breast:
18	chr6:44261562..44267016-chr6:44278207..44281216,9	MCF-7	breast:
19	chr6:44094457..44097245-chr6:44270465..44272999,2	K562	blood:
20	chr6:44273300..44278087-chr6:44284295..44289273,5	MCF-7	breast:
21	chr6:44140189..44140717-chr6:44272658..44273173,2	K562	blood:
22	chr6:44215194..44217832-chr6:44265456..44268236,2	K562	blood:
23	chr6:44272651..44274712-chr6:44338316..44340561,2	K562	blood:
24	chr6:44244057..44246531-chr6:44270330..44272647,2	MCF-7	breast:
25	chr6:44257360..44259617-chr6:44265641..44268497,2	MCF-7	breast:

Variant related genes	Relation type
AARS2	TF binding region
TCTE1	TF binding region
AARS2	CpG island
TCTE1	CpG island
ENSG00000178233	chromatin interactions
ENSG00000137216	chromatin interactions
ENSG00000146232	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000124608	chromatin interactions
ENSG00000157593	chromatin interactions
ENSG00000265700	chromatin interactions
ENSG00000146221	chromatin interactions
ENSG00000272442	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000180992	chromatin interactions

Extended variants
information (count: 481 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:481 , 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	rs1056093	chr6:44266574-44266575	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560147400	chr6:44266600-44266601	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs200024856	chr6:44266644-44266645	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs77661824	chr6:44266648-44266649	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs5875874	chr6:44266649-44266650	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs112912251	chr6:44266652-44266653	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs191775695	chr6:44266667-44266668	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs1056092	chr6:44266708-44266709	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs548185310	chr6:44266748-44266749	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs149714606	chr6:44266773-44266774	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs116579451	chr6:44266811-44266812	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs527555633	chr6:44266812-44266813	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs147288256	chr6:44266827-44266828	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs552452554	chr6:44266866-44266867	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs570508703	chr6:44266902-44266903	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs538044094	chr6:44266923-44266924	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs534416	chr6:44266925-44266926	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs370057942	chr6:44266958-44266959	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs535583490	chr6:44266964-44266965	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs553722790	chr6:44266974-44266975	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs1123523	chr6:44266984-44266985	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs201274623	chr6:44266997-44266998	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs35562884	chr6:44267000-44267001	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs76864619	chr6:44267007-44267008	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs370809816	chr6:44267009-44267010	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs184321024	chr6:44267044-44267045	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs558424002	chr6:44267056-44267057	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs576704345	chr6:44267063-44267064	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs544014735	chr6:44267155-44267156	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs112521684	chr6:44267171-44267172	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs74438062	chr6:44267183-44267184	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs562294322	chr6:44267191-44267192	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs189010551	chr6:44267195-44267196	Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs541960326	chr6:44267209-44267210	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs114920585	chr6:44267211-44267212	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs527281365	chr6:44267239-44267240	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs538721769	chr6:44267277-44267278	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs146753959	chr6:44267287-44267288	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs192274662	chr6:44267302-44267303	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs549544750	chr6:44267343-44267344	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs76458008	chr6:44267358-44267359	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs115747904	chr6:44267379-44267380	Weak transcription Strong transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs185382031	chr6:44267561-44267562	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547495063	chr6:44267564-44267565	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs140359685	chr6:44267566-44267567	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs370436608	chr6:44267600-44267601	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs139671693	chr6:44267640-44267641	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs202135465	chr6:44267649-44267650	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs200470637	chr6:44267650-44267651	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs72214655	chr6:44267651-44267652	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
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
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
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
Cancer	20164920	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44265000-44268000	Weak transcription	Dnd41	blood
2	chr6:44265000-44269800	Weak transcription	Hela-S3	cervix
3	chr6:44265400-44268000	Weak transcription	Aorta	Aorta
4	chr6:44265600-44268000	Weak transcription	HepG2	liver
5	chr6:44265600-44268200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr6:44265600-44279600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr6:44265800-44266600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:44265800-44268000	Weak transcription	HSMM	muscle
9	chr6:44265800-44269400	Weak transcription	K562	blood
10	chr6:44265800-44270000	Weak transcription	HMEC	breast
11	chr6:44266000-44266800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:44266000-44266800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr6:44266000-44267800	Weak transcription	Brain Substantia Nigra	brain
14	chr6:44266000-44268000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:44266000-44268000	Weak transcription	Primary T cells from cord blood	blood
16	chr6:44266000-44268000	Weak transcription	Brain Angular Gyrus	brain
17	chr6:44266000-44268000	Weak transcription	Brain Anterior Caudate	brain
18	chr6:44266000-44268000	Weak transcription	Left Ventricle	heart
19	chr6:44266000-44268000	Weak transcription	Ovary	ovary
20	chr6:44266000-44268000	Weak transcription	Right Ventricle	heart
21	chr6:44266000-44268000	Weak transcription	Spleen	Spleen
22	chr6:44266000-44268000	Weak transcription	A549	lung
23	chr6:44266000-44268200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr6:44266000-44268200	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr6:44266000-44268200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr6:44266000-44268200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr6:44266000-44269800	Weak transcription	GM12878-XiMat	blood
28	chr6:44266000-44271600	Weak transcription	NHDF-Ad	bronchial
29	chr6:44266000-44272400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr6:44266000-44276600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr6:44266000-44277000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr6:44266000-44280000	Weak transcription	Small Intestine	intestine
33	chr6:44266200-44266600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr6:44266200-44266800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:44266200-44267400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr6:44266200-44267400	Weak transcription	Liver	Liver
37	chr6:44266200-44267400	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr6:44266200-44267800	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr6:44266200-44268000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:44266200-44268000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr6:44266200-44268000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr6:44266200-44268000	Weak transcription	Primary B cells from peripheral blood	blood
43	chr6:44266200-44268000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr6:44266200-44268000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr6:44266200-44268000	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr6:44266200-44268000	Weak transcription	Adipose Nuclei	Adipose
47	chr6:44266200-44268000	Weak transcription	Brain Hippocampus Middle	brain
48	chr6:44266200-44268000	Weak transcription	Pancreas	Pancrea
49	chr6:44266200-44268000	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr6:44266200-44268400	Weak transcription	Rectal Smooth Muscle	rectum

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