Variant report

Variant	nsv528715
Chromosome Location	chr7:3451251-3598581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:927)
CpG islands
(count:489)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:927 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:3563621-3563954	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:3515387-3515402	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:3519977-3520319	K562	blood:	n/a	n/a
4	BRCA1	chr7:3522141-3522202	GM12878	blood:	n/a	n/a
5	CEBPB	chr7:3526587-3526825	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:3479036-3479317	K562	blood:	n/a	chr7:3479156-3479167
7	CEBPB	chr7:3522089-3522651	Hela-S3	cervix:	n/a	chr7:3522481-3522492
8	CEBPB	chr7:3522246-3522685	A549	lung:	n/a	chr7:3522481-3522492
9	CEBPB	chr7:3591680-3591787	K562	blood:	n/a	n/a
10	CEBPB	chr7:3475761-3476128	IMR90	lung:	n/a	chr7:3475940-3475949 chr7:3475939-3475950 chr7:3475940-3475949
11	CEBPB	chr7:3478893-3479425	A549	lung:	n/a	chr7:3479156-3479167
12	CEBPB	chr7:3478910-3479342	MCF-7	breast:	n/a	chr7:3479156-3479167
13	CEBPB	chr7:3533115-3533486	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:3515364-3515642	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:3540105-3540112	K562	blood:	n/a	n/a
16	CEBPB	chr7:3522361-3522623	K562	blood:	n/a	chr7:3522481-3522492
17	CEBPB	chr7:3533031-3533530	A549	lung:	n/a	n/a
18	CEBPB	chr7:3478988-3479368	ECC-1	luminal epithelium:	n/a	chr7:3479156-3479167
19	CEBPB	chr7:3533116-3533450	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:3478938-3479358	Hela-S3	cervix:	n/a	chr7:3479156-3479167
21	CEBPB	chr7:3521976-3522775	MCF-7	breast:	n/a	chr7:3522481-3522492
22	CEBPB	chr7:3481954-3482057	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:3534870-3535070	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:3478986-3479323	HepG2	liver:	n/a	chr7:3479156-3479167
25	CEBPB	chr7:3515429-3515566	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:3457543-3457997	H1-hESC	embryonic stem cell:	n/a	chr7:3457585-3457598 chr7:3457585-3457598
27	CEBPB	chr7:3478943-3479301	ECC-1	luminal epithelium:	n/a	chr7:3479156-3479167
28	CEBPB	chr7:3515347-3515593	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:3551480-3551693	K562	blood:	n/a	chr7:3551564-3551575
30	CEBPB	chr7:3475773-3476125	HepG2	liver:	n/a	chr7:3475940-3475949 chr7:3475939-3475950 chr7:3475940-3475949
31	CEBPB	chr7:3551459-3551660	H1-hESC	embryonic stem cell:	n/a	chr7:3551564-3551575
32	CEBPB	chr7:3475791-3476051	A549	lung:	n/a	chr7:3475940-3475949 chr7:3475939-3475950 chr7:3475940-3475949
33	CEBPB	chr7:3533215-3533381	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:3522301-3522671	HepG2	liver:	n/a	chr7:3522481-3522492
35	CEBPB	chr7:3551499-3551703	HepG2	liver:	n/a	chr7:3551564-3551575
36	CEBPB	chr7:3491434-3491634	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:3515281-3515612	MCF-7	breast:	n/a	n/a
38	CEBPB	chr7:3479035-3479306	H1-hESC	embryonic stem cell:	n/a	chr7:3479156-3479167
39	CEBPB	chr7:3522143-3522706	MCF-7	breast:	n/a	chr7:3522481-3522492
40	CEBPB	chr7:3486445-3486801	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:3515394-3515623	A549	lung:	n/a	n/a
42	CEBPB	chr7:3522164-3522619	HCT-116	colon:	n/a	chr7:3522481-3522492
43	CEBPB	chr7:3522183-3522654	H1-hESC	embryonic stem cell:	n/a	chr7:3522481-3522492
44	CEBPB	chr7:3579181-3579258	A549	lung:	n/a	n/a
45	CEBPB	chr7:3522175-3522675	A549	lung:	n/a	chr7:3522481-3522492
46	CEBPB	chr7:3471268-3471422	HepG2	liver:	n/a	chr7:3471347-3471358
47	CEBPB	chr7:3478751-3479563	A549	lung:	n/a	chr7:3479156-3479167
48	CEBPB	chr7:3522292-3522669	IMR90	lung:	n/a	chr7:3522481-3522492
49	CEBPB	chr7:3476192-3476839	A549	lung:	n/a	n/a
50	CEBPB	chr7:3471229-3471499	HepG2	liver:	n/a	chr7:3471347-3471358

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3533958-3534008	NHBE	bronchial:	n/a
2	chr7:3533958-3534008	NHBE	bronchial:	n/a
3	chr7:3488816-3488866	HRCEpiC	kidney:	n/a
4	chr7:3533958-3534008	SK-N-SH_RA	brain:	n/a
5	chr7:3478077-3478127	SK-N-SH_RA	brain:	n/a
6	chr7:3588642-3588692	SK-N-SH_RA	brain:	n/a
7	chr7:3488816-3488866	Caco-2	colon:	n/a
8	chr7:3488816-3488866	BJ	skin:	n/a
9	chr7:3488816-3488866	HEK293	kidney:	embryo
10	chr7:3478077-3478127	HL-60	blood:	n/a
11	chr7:3536689-3536739	Jurkat	blood:	n/a
12	chr7:3470434-3470484	NB4	blood:	n/a
13	chr7:3588642-3588692	HUVEC	blood vessel:	n/a
14	chr7:3478077-3478127	GM12891	blood:	n/a
15	chr7:3549961-3550011	SK-N-MC	brain:	n/a
16	chr7:3470434-3470484	Caco-2	colon:	n/a
17	chr7:3533958-3534008	NB4	blood:	n/a
18	chr7:3488816-3488866	HCPEpiC	choroid plexus:	n/a
19	chr7:3488816-3488866	SK-N-SH_RA	brain:	n/a
20	chr7:3536689-3536739	Caco-2	colon:	n/a
21	chr7:3470434-3470484	HCT-116	colon:	n/a
22	chr7:3588642-3588692	HMEC	breast:	n/a
23	chr7:3577053-3577103	HIPEpiC	eye:	n/a
24	chr7:3549961-3550011	T-47D	breast:	n/a
25	chr7:3549961-3550011	AG04449	skin:	fetal
26	chr7:3488816-3488866	ECC-1	luminal epithelium:	n/a
27	chr7:3533958-3534008	U87	brain:	n/a
28	chr7:3470434-3470484	GM19239	blood:	n/a
29	chr7:3488816-3488866	NHDF-neo	bronchial:	n/a
30	chr7:3488816-3488866	SK-N-MC	brain:	n/a
31	chr7:3478077-3478127	Jurkat	blood:	n/a
32	chr7:3533958-3534008	GM12878	blood:	n/a
33	chr7:3470434-3470484	ProgFib	skin:	n/a
34	chr7:3536689-3536739	ProgFib	skin:	n/a
35	chr7:3533958-3534008	HAEpiC	amniotic membrane:	n/a
36	chr7:3588642-3588692	H1-hESC	embryonic stem cell:	embryo
37	chr7:3536689-3536739	AG09309	skin:	n/a
38	chr7:3488816-3488866	Hepatocyte	liver:	n/a
39	chr7:3549961-3550011	CMK	blood:	n/a
40	chr7:3577053-3577103	HAEpiC	amniotic membrane:	n/a
41	chr7:3478077-3478127	PANC-1	pancreas:	n/a
42	chr7:3478077-3478127	HNPCEpiC	eye:	n/a
43	chr7:3549961-3550011	HCT-116	colon:	n/a
44	chr7:3536689-3536739	BJ	skin:	n/a
45	chr7:3488816-3488866	AG09309	skin:	n/a
46	chr7:3470434-3470484	NH-A	brain:	n/a
47	chr7:3588642-3588692	HCF	heart:	n/a
48	chr7:3588642-3588692	AoSMC	blood vessel:	n/a
49	chr7:3470434-3470484	SK-N-SH_RA	brain:	n/a
50	chr7:3470434-3470484	PANC-1	pancreas:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3596799..3598779-chr7:3598841..3601044,2	K562	blood:
2	chr7:3452987..3455737-chr7:3457417..3460056,3	MCF-7	breast:
3	chr7:3581196..3583334-chr7:3583848..3586419,2	K562	blood:
4	chr7:3577804..3580555-chr7:3590884..3593146,2	MCF-7	breast:
5	chr7:3522949..3523470-chr7:3687761..3688597,2	MCF-7	breast:
6	chr7:3537080..3539372-chr7:3543955..3546696,2	MCF-7	breast:
7	chr7:3441889..3444490-chr7:3452543..3454242,2	MCF-7	breast:
8	chr7:3555349..3557729-chr7:3560043..3561605,2	K562	blood:
9	chr7:3466489..3468571-chr7:3470496..3474286,3	MCF-7	breast:
10	chr7:3444122..3444632-chr7:3471439..3472016,2	MCF-7	breast:
11	chr7:3521340..3522302-chr7:4671144..4671918,2	MCF-7	breast:
12	chr7:3551543..3553743-chr7:3556409..3559283,2	MCF-7	breast:
13	chr7:3439202..3440208-chr7:3521793..3522518,3	MCF-7	breast:
14	chr7:3537080..3539372-chr7:3543955..3546696,2	MCF-7	breast:
15	chr7:3546340..3548906-chr7:3559233..3561540,2	MCF-7	breast:
16	chr7:3463184..3466150-chr7:3469039..3471328,2	MCF-7	breast:
17	chr7:3551543..3553743-chr7:3556409..3559283,2	MCF-7	breast:
18	chr7:3450055..3452486-chr7:3794915..3797670,2	MCF-7	breast:
19	chr7:3339718..3341766-chr7:3458306..3459954,2	K562	blood:
20	chr7:3598045..3599826-chr7:3607481..3609986,2	K562	blood:
21	chr7:3528452..3531258-chr7:3533365..3536191,2	MCF-7	breast:
22	chr7:3525893..3527972-chr7:3528761..3530519,2	K562	blood:
23	chr7:3581196..3583334-chr7:3583848..3586419,2	K562	blood:
24	chr7:3553060..3555067-chr7:3563741..3566106,2	MCF-7	breast:
25	chr7:3528452..3531258-chr7:3533365..3536191,2	MCF-7	breast:
26	chr7:3521696..3522495-chr7:3631928..3632648,2	MCF-7	breast:
27	chr7:3551947..3554691-chr7:3562735..3565041,2	MCF-7	breast:
28	chr7:3555349..3557729-chr7:3560043..3561605,2	K562	blood:
29	chr7:3467584..3469607-chr7:3473579..3476455,2	MCF-7	breast:
30	chr7:3553060..3555067-chr7:3563741..3566106,2	MCF-7	breast:
31	chr7:3467584..3469607-chr7:3473579..3476455,2	MCF-7	breast:
32	chr7:3521755..3523053-chr7:3688631..3689551,7	MCF-7	breast:
33	chr7:3551947..3554691-chr7:3562735..3565041,2	MCF-7	breast:
34	chr7:3444047..3446365-chr7:3452049..3455174,3	MCF-7	breast:
35	chr7:3466489..3468571-chr7:3470496..3474286,3	MCF-7	breast:
36	chr6:34331825..34332645-chr7:3565574..3566479,2	MCF-7	breast:
37	chr7:3463184..3466150-chr7:3469039..3471328,2	MCF-7	breast:
38	chr7:3546340..3548906-chr7:3559233..3561540,2	MCF-7	breast:
39	chr7:3340840..3343338-chr7:3476351..3477939,2	MCF-7	breast:
40	chr7:3525893..3527972-chr7:3528761..3530519,2	K562	blood:
41	chr7:3577804..3580555-chr7:3590884..3593146,2	MCF-7	breast:
42	chr7:3521823..3522640-chr7:3807742..3808264,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000211544	TF binding region
ENSG00000211544	CpG island
ENSG00000236708	chromatin interactions
ENSG00000211544	chromatin interactions
ENSG00000146555	chromatin interactions

Extended variants
information (count: 8640 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:8640 , 50 per page) page: 1 2 3 4 5 6 7 ... 173

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6959573	chr7:3451251-3451252	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148966137	chr7:3451254-3451255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181573208	chr7:3451266-3451267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186365716	chr7:3451271-3451272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4719923	chr7:3451280-3451281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143688849	chr7:3451286-3451287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574835996	chr7:3451334-3451335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199866841	chr7:3451343-3451344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148087545	chr7:3451368-3451369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191268677	chr7:3451375-3451376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546123263	chr7:3451378-3451379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183370870	chr7:3451403-3451404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185884739	chr7:3451411-3451412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs58692075	chr7:3451428-3451429	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs115407290	chr7:3451455-3451456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190000733	chr7:3451479-3451480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183366802	chr7:3451525-3451526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187914398	chr7:3451542-3451543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34645214	chr7:3451544-3451545	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs532920304	chr7:3451555-3451556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527539653	chr7:3451591-3451592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376743746	chr7:3451600-3451601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566709336	chr7:3451605-3451606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529083909	chr7:3451669-3451670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192005644	chr7:3451705-3451706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568954381	chr7:3451706-3451707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183096340	chr7:3451737-3451738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188154727	chr7:3451762-3451763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531043208	chr7:3451778-3451779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369782215	chr7:3451846-3451847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570528923	chr7:3451866-3451867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539421603	chr7:3451872-3451873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192639817	chr7:3451882-3451883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573442766	chr7:3451897-3451898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542151745	chr7:3451912-3451913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73298394	chr7:3451936-3451937	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs77144821	chr7:3451951-3451952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141824784	chr7:3451981-3451982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117217710	chr7:3452005-3452006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532958158	chr7:3452006-3452007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540192711	chr7:3452021-3452022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369321297	chr7:3452029-3452030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529233152	chr7:3452058-3452059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74633154	chr7:3452120-3452121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185027108	chr7:3452166-3452167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531369539	chr7:3452189-3452190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73298396	chr7:3452257-3452258	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs73298397	chr7:3452301-3452302	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs539456720	chr7:3452335-3452336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34077951	chr7:3452338-3452339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:82)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:826 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3444400-3451800	Weak transcription	Fetal Brain Female	brain
2	chr7:3444800-3454800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr7:3447000-3457000	Weak transcription	Fetal Kidney	kidney
4	chr7:3449400-3456200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:3449400-3456200	Weak transcription	Aorta	Aorta
6	chr7:3450200-3451600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr7:3450400-3451400	Enhancers	Fetal Brain Male	brain
8	chr7:3450600-3452000	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr7:3450600-3452400	Weak transcription	Pancreas	Pancrea
10	chr7:3451400-3456000	Weak transcription	Fetal Brain Male	brain
11	chr7:3451600-3453000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr7:3451800-3452800	Enhancers	Fetal Brain Female	brain
13	chr7:3452000-3453000	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr7:3453000-3454400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr7:3454200-3454600	Weak transcription	NHEK	skin
16	chr7:3454400-3456000	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr7:3454800-3455600	Enhancers	NHEK	skin
18	chr7:3454800-3455800	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr7:3454800-3456800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:3454800-3457600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:3455200-3456400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:3455400-3456000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:3455400-3456400	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr7:3455600-3455800	Flanking Active TSS	NHEK	skin
25	chr7:3455800-3456000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:3455800-3456000	Enhancers	NHEK	skin
27	chr7:3456000-3456200	Enhancers	Fetal Brain Male	brain
28	chr7:3456000-3456200	Flanking Active TSS	NHEK	skin
29	chr7:3456000-3456400	Enhancers	Fetal Intestine Large	intestine
30	chr7:3456000-3457200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:3456000-3460200	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr7:3456200-3456400	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr7:3456200-3456800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:3456200-3457600	Enhancers	NHEK	skin
35	chr7:3456600-3457600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr7:3456800-3465800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:3457000-3457400	Enhancers	Fetal Kidney	kidney
38	chr7:3457000-3457600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:3457000-3457600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr7:3457200-3457600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:3457200-3457600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:3457200-3457800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr7:3458400-3459200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:3458400-3465800	Weak transcription	Pancreas	Pancrea
45	chr7:3460200-3460400	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr7:3465000-3470200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:3465800-3466000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:3465800-3466000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:3465800-3466000	Enhancers	H9 Cell Line	embryonic stem cell
50	chr7:3465800-3466000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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