Variant report

Variant	nsv878479
Chromosome Location	chr4:3461900-3498896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1263)
CpG islands
(count:3358)
Chromatin interactive
region (count:73)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1263 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:3482298-3482759	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:3482260-3482611	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:3482512-3482601	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:3496152-3496215	K562	blood:	n/a	n/a
5	BACH1	chr4:3482323-3482523	K562	blood:	n/a	n/a
6	BATF	chr4:3491237-3491472	GM12878	blood:	n/a	n/a
7	BCL3	chr4:3469104-3469626	GM12878	blood:	n/a	n/a
8	BCL3	chr4:3475204-3475428	GM12878	blood:	n/a	n/a
9	BCL3	chr4:3469218-3469567	GM12878	blood:	n/a	n/a
10	BCL3	chr4:3475144-3475461	GM12878	blood:	n/a	n/a
11	BCL3	chr4:3469865-3471115	GM12878	blood:	n/a	n/a
12	BCL3	chr4:3469863-3470991	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:3486390-3486566	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:3491263-3491395	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:3496279-3496546	HepG2	liver:	n/a	chr4:3496388-3496404
16	BHLHE40	chr4:3472328-3472516	K562	blood:	n/a	n/a
17	BHLHE40	chr4:3479250-3479561	HepG2	liver:	n/a	chr4:3479409-3479418 chr4:3479409-3479418 chr4:3479408-3479417 chr4:3479403-3479424
18	BHLHE40	chr4:3472381-3472564	HepG2	liver:	n/a	n/a
19	BHLHE40	chr4:3482294-3482545	K562	blood:	n/a	n/a
20	BHLHE40	chr4:3478312-3478492	HepG2	liver:	n/a	n/a
21	BHLHE40	chr4:3479316-3479464	K562	blood:	n/a	chr4:3479409-3479418 chr4:3479409-3479418 chr4:3479408-3479417 chr4:3479403-3479424
22	BHLHE40	chr4:3486975-3487201	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:3482383-3482568	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:3480551-3480684	K562	blood:	n/a	n/a
25	BHLHE40	chr4:3469254-3469426	K562	blood:	n/a	n/a
26	BHLHE40	chr4:3471344-3471419	HepG2	liver:	n/a	n/a
27	BHLHE40	chr4:3482321-3482582	HepG2	liver:	n/a	n/a
28	BRCA1	chr4:3482384-3482586	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr4:3482275-3482539	H1-hESC	embryonic stem cell:	n/a	n/a
30	CBX3	chr4:3482279-3482637	K562	blood:	n/a	n/a
31	CCNT2	chr4:3480418-3480529	K562	blood:	n/a	n/a
32	CCNT2	chr4:3482381-3482557	K562	blood:	n/a	n/a
33	CCNT2	chr4:3465851-3465998	K562	blood:	n/a	n/a
34	CEBPB	chr4:3482226-3482506	MCF-7	breast:	n/a	n/a
35	CEBPB	chr4:3482295-3482572	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:3482236-3482560	K562	blood:	n/a	n/a
37	CEBPB	chr4:3482224-3482577	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:3482205-3482557	K562	blood:	n/a	n/a
39	CEBPB	chr4:3493665-3493953	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:3482254-3482576	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:3482210-3482696	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr4:3482279-3482561	A549	lung:	n/a	n/a
43	CEBPB	chr4:3482293-3482579	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:3485772-3486821	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPD	chr4:3498169-3498383	HepG2	liver:	n/a	n/a
46	CHD1	chr4:3482157-3482731	IMR90	lung:	n/a	n/a
47	CHD2	chr4:3496377-3496397	K562	blood:	n/a	n/a
48	CHD2	chr4:3486927-3487016	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr4:3482312-3482602	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr4:3486913-3487328	GM12878	blood:	n/a	n/a

(count:3358 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3475262-3475312	HUVEC	blood vessel:	n/a
2	chr4:3475262-3475312	Caco-2	colon:	n/a
3	chr4:3462498-3462548	SK-N-SH	brain:	n/a
4	chr4:3475262-3475312	HUVEC	blood vessel:	n/a
5	chr4:3475262-3475312	Caco-2	colon:	n/a
6	chr4:3462498-3462548	SK-N-SH	brain:	n/a
7	chr4:3465367-3465417	GM12892	blood:	n/a
8	chr4:3480318-3480368	HRPEpiC	eye:	n/a
9	chr4:3465367-3465417	HEK293	kidney:	embryo
10	chr4:3471901-3471951	GM12892	blood:	n/a
11	chr4:3485393-3485443	NHDF-neo	bronchial:	n/a
12	chr4:3469040-3469090	BJ	skin:	n/a
13	chr4:3464754-3464804	NH-A	brain:	n/a
14	chr4:3482507-3482557	SK-N-SH	brain:	n/a
15	chr4:3475372-3475422	SKMC	muscle:	n/a
16	chr4:3486380-3486430	U87	brain:	n/a
17	chr4:3475328-3475378	SK-N-SH_RA	brain:	n/a
18	chr4:3486116-3486166	NT2-D1	testis:	n/a
19	chr4:3475328-3475378	AoSMC	blood vessel:	n/a
20	chr4:3480656-3480706	CMK	blood:	n/a
21	chr4:3489931-3489981	ECC-1	luminal epithelium:	n/a
22	chr4:3495341-3495391	IMR90	lung:	fetal
23	chr4:3494883-3494933	HUVEC	blood vessel:	n/a
24	chr4:3468188-3468238	Jurkat	blood:	n/a
25	chr4:3478209-3478259	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:3473232-3473282	A549	lung:	n/a
27	chr4:3465064-3465114	HCPEpiC	choroid plexus:	n/a
28	chr4:3471397-3471447	HIPEpiC	eye:	n/a
29	chr4:3480318-3480368	AG09309	skin:	n/a
30	chr4:3489931-3489981	AG09309	skin:	n/a
31	chr4:3475262-3475312	HCPEpiC	choroid plexus:	n/a
32	chr4:3471901-3471951	AG04450	lung:	fetal
33	chr4:3480318-3480368	MCF-7	breast:	n/a
34	chr4:3489931-3489981	HNPCEpiC	eye:	n/a
35	chr4:3464702-3464752	Jurkat	blood:	n/a
36	chr4:3494582-3494632	U87	brain:	n/a
37	chr4:3473450-3473500	Jurkat	blood:	n/a
38	chr4:3473737-3473787	HAEpiC	amniotic membrane:	n/a
39	chr4:3489931-3489981	NHBE	bronchial:	n/a
40	chr4:3495242-3495292	PFSK-1	brain:	n/a
41	chr4:3464996-3465046	SAEC	small airway:	n/a
42	chr4:3486204-3486254	PrEC	prostate:	n/a
43	chr4:3478064-3478114	HIPEpiC	eye:	n/a
44	chr4:3487334-3487384	H1-hESC	embryonic stem cell:	embryo
45	chr4:3464998-3465048	HCT-116	colon:	n/a
46	chr4:3473595-3473645	Hepatocyte	liver:	n/a
47	chr4:3478064-3478114	AG09309	skin:	n/a
48	chr4:3478348-3478398	T-47D	breast:	n/a
49	chr4:3473450-3473500	HRPEpiC	eye:	n/a
50	chr4:3475233-3475283	U87	brain:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3462844..3463532-chr4:3486166..3487066,3	MCF-7	breast:
2	chr4:3418569..3420412-chr4:3484561..3487471,2	MCF-7	breast:
3	chr4:3075047..3077442-chr4:3472520..3475162,3	K562	blood:
4	chr11:61737950..61740369-chr4:3461504..3464468,2	MCF-7	breast:
5	chr4:3464614..3465179-chr4:3486100..3486697,2	MCF-7	breast:
6	chr4:3110927..3117533-chr4:3461507..3465762,15	MCF-7	breast:
7	chr4:3293993..3296488-chr4:3491954..3495229,3	MCF-7	breast:
8	chr4:3491033..3494897-chr4:3496204..3500010,5	K562	blood:
9	chr4:3498309..3502581-chr4:3507036..3510283,5	MCF-7	breast:
10	chr4:3294365..3296058-chr4:3468605..3470363,2	MCF-7	breast:
11	chr4:3489490..3491516-chr4:3532625..3534130,2	K562	blood:
12	chr4:3488541..3491242-chr4:3495615..3498535,2	K562	blood:
13	chr4:3490007..3491895-chr4:3517979..3519812,2	K562	blood:
14	chr4:3386285..3389665-chr4:3485168..3487566,3	MCF-7	breast:
15	chr4:3497012..3499150-chr4:3532552..3535474,2	K562	blood:
16	chr4:3483725..3485778-chr4:3827881..3829780,2	MCF-7	breast:
17	chr4:3354072..3356995-chr4:3479067..3480969,2	MCF-7	breast:
18	chr4:3484197..3487656-chr4:3491883..3496058,4	K562	blood:
19	chr4:3481101..3483332-chr4:3533329..3535150,2	MCF-7	breast:
20	chr4:3113077..3115750-chr4:3467353..3469747,2	MCF-7	breast:
21	chr4:3346041..3348825-chr4:3461682..3464499,2	MCF-7	breast:
22	chr4:3464667..3465179-chr4:3486678..3487324,2	MCF-7	breast:
23	chr4:3372799..3374407-chr4:3477096..3479436,2	MCF-7	breast:
24	chr4:3464939..3465859-chr4:3486070..3487026,3	MCF-7	breast:
25	chr4:3365688..3366496-chr4:3463170..3464043,2	MCF-7	breast:
26	chr4:3439130..3442230-chr4:3483136..3486025,3	MCF-7	breast:
27	chr4:3231157..3234122-chr4:3467560..3470032,2	MCF-7	breast:
28	chr4:3346980..3350932-chr4:3475951..3478417,3	MCF-7	breast:
29	chr4:3464629..3465770-chr4:3486550..3487347,4	MCF-7	breast:
30	chr4:3496237..3498612-chr4:3527624..3529896,2	K562	blood:
31	chr4:3487684..3490277-chr4:3491908..3495748,6	K562	blood:
32	chr4:3481541..3484039-chr4:3515010..3518175,3	MCF-7	breast:
33	chr4:3495267..3497538-chr4:3499931..3501588,2	K562	blood:
34	chr4:3108064..3109057-chr4:3481789..3482473,3	K562	blood:
35	chr4:3485927..3488368-chr4:3533732..3536345,3	MCF-7	breast:
36	chr4:3464667..3465179-chr4:3486678..3487324,2	MCF-7	breast:
37	chr4:3215167..3215891-chr4:3479590..3480357,2	K562	blood:
38	chr4:3497012..3500128-chr4:3532348..3534141,3	K562	blood:
39	chr4:3464614..3465179-chr4:3486100..3486697,2	MCF-7	breast:
40	chr4:3445342..3446316-chr4:3482040..3482882,2	K562	blood:
41	chr4:3082342..3084920-chr4:3490322..3492500,2	K562	blood:
42	chr4:3471602..3475518-chr4:3476351..3479966,4	K562	blood:
43	chr4:3478548..3481215-chr4:3487290..3489311,2	K562	blood:
44	chr4:3428894..3431544-chr4:3462169..3465013,2	MCF-7	breast:
45	chr4:3471602..3475518-chr4:3476351..3479966,4	K562	blood:
46	chr4:3481020..3484183-chr4:3488790..3491004,5	K562	blood:
47	chr4:3343221..3349626-chr4:3462156..3471133,16	MCF-7	breast:
48	chr4:3292471..3295854-chr4:3462941..3467927,8	MCF-7	breast:
49	chr4:3488541..3491242-chr4:3495615..3498535,2	K562	blood:
50	chr4:3462755..3463727-chr4:3486334..3487219,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRPAP1-4	chr4:3480710-3483420	ucscGeneNc_uc003ghh_2

No data

Variant related genes	Relation type
DOK7	TF binding region
DOK7	CpG island
ENSG00000109758	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000110619	chromatin interactions
ENSG00000197386	chromatin interactions
ENSG00000159788	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000251075	chromatin interactions

Extended variants
information (count: 2585 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2585 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2091626	chr4:3461900-3461901	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575838477	chr4:3461942-3461943	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546522498	chr4:3461943-3461944	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs542580025	chr4:3461957-3461958	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs528574768	chr4:3461962-3461963	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs113596337	chr4:3462063-3462064	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs572531747	chr4:3462074-3462075	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544700493	chr4:3462076-3462077	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs547324374	chr4:3462082-3462083	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs370200351	chr4:3462126-3462127	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs116836670	chr4:3462150-3462151	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs544350547	chr4:3462154-3462155	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs150975826	chr4:3462185-3462186	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs1076903	chr4:3462194-3462195	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs547014613	chr4:3462196-3462197	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs140836554	chr4:3462233-3462234	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs145416785	chr4:3462262-3462263	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs368893829	chr4:3462360-3462361	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs532600710	chr4:3462369-3462370	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs528715859	chr4:3462414-3462415	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs116881258	chr4:3462447-3462448	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs149183522	chr4:3462453-3462454	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569333494	chr4:3462464-3462465	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs189524195	chr4:3462469-3462470	Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs146018601	chr4:3462498-3462499	Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs116609676	chr4:3462499-3462500	Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs376027675	chr4:3462501-3462502	Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs73079073	chr4:3462525-3462526	Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs193224376	chr4:3462531-3462532	Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs138904541	chr4:3462540-3462541	Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs369094256	chr4:3462591-3462592	Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs572494846	chr4:3462609-3462610	ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs538204063	chr4:3462637-3462638	ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs558130089	chr4:3462664-3462665	ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs562838581	chr4:3462674-3462675	ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs529260361	chr4:3462789-3462790	ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs551006960	chr4:3462842-3462843	Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs373162187	chr4:3462916-3462917	Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs574963821	chr4:3462923-3462924	Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs185182042	chr4:3462940-3462941	Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs190077876	chr4:3462954-3462955	Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs530041167	chr4:3462974-3462975	Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs181426108	chr4:3463032-3463033	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs552558907	chr4:3463086-3463087	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs562893891	chr4:3463142-3463143	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs531806476	chr4:3463168-3463169	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs548420962	chr4:3463182-3463183	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs567450584	chr4:3463215-3463216	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs141491753	chr4:3463221-3463222	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs546783080	chr4:3463225-3463226	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3454400-3462400	Weak transcription	HSMM	muscle
2	chr4:3454600-3462400	Weak transcription	Pancreas	Pancrea
3	chr4:3461000-3463000	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr4:3462000-3462400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:3462000-3462800	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr4:3462000-3463800	Enhancers	HSMMtube	muscle
7	chr4:3462000-3464000	Enhancers	Fetal Muscle Leg	muscle
8	chr4:3462400-3463600	Enhancers	HSMM	muscle
9	chr4:3462400-3463800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr4:3462400-3464800	Enhancers	Pancreas	Pancrea
11	chr4:3462600-3463200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:3462600-3464000	Enhancers	Stomach Mucosa	stomach
13	chr4:3462600-3464200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:3462600-3464200	Enhancers	Stomach Smooth Muscle	stomach
15	chr4:3462600-3464600	Enhancers	Gastric	stomach
16	chr4:3462600-3464600	Enhancers	Right Ventricle	heart
17	chr4:3462600-3464800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:3462600-3464800	Enhancers	Fetal Heart	heart
19	chr4:3462600-3464800	Enhancers	Left Ventricle	heart
20	chr4:3462600-3465000	Enhancers	HMEC	breast
21	chr4:3462600-3465800	Enhancers	Liver	Liver
22	chr4:3462800-3463000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:3462800-3463000	Enhancers	Hela-S3	cervix
24	chr4:3462800-3463200	Bivalent Enhancer	NHEK	skin
25	chr4:3462800-3463400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:3462800-3463800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr4:3462800-3463800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
28	chr4:3462800-3463800	Enhancers	Aorta	Aorta
29	chr4:3462800-3463800	Enhancers	Esophagus	oesophagus
30	chr4:3462800-3464400	Enhancers	Lung	lung
31	chr4:3462800-3464800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr4:3463000-3463200	Bivalent/Poised TSS	HepG2	liver
33	chr4:3463000-3463400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr4:3463000-3463400	Flanking Active TSS	Hela-S3	cervix
35	chr4:3463000-3464000	Enhancers	Duodenum Mucosa	Duodenum
36	chr4:3463000-3464000	Enhancers	Psoas Muscle	Psoas
37	chr4:3463000-3464800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:3463000-3464800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr4:3463200-3463400	Flanking Bivalent TSS/Enh	HepG2	liver
40	chr4:3463200-3463400	Flanking Bivalent TSS/Enh	NHEK	skin
41	chr4:3463200-3463600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:3463200-3464200	Bivalent Enhancer	Colonic Mucosa	Colon
43	chr4:3463200-3464200	Enhancers	GM12878-XiMat	blood
44	chr4:3463200-3465600	Bivalent Enhancer	Placenta	Placenta
45	chr4:3463400-3463600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr4:3463400-3463600	Bivalent Enhancer	Fetal Stomach	stomach
47	chr4:3463400-3463800	Enhancers	Fetal Brain Male	brain
48	chr4:3463400-3463800	Bivalent Enhancer	HepG2	liver
49	chr4:3463400-3464200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr4:3463400-3464800	Bivalent Enhancer	Primary B cells from peripheral blood	blood

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