Variant report

Variant	nsv886100
Chromosome Location	chr6:68033877-68186228
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	ARID3A	chr6:68071467-68071820	K562	blood:	n/a	n/a
2	ATF1	chr6:68072771-68073293	K562	blood:	n/a	n/a
3	ATF1	chr6:68143118-68143403	K562	blood:	n/a	n/a
4	ATF3	chr6:68143086-68143416	K562	blood:	n/a	n/a
5	ATF3	chr6:68062647-68062891	K562	blood:	n/a	n/a
6	BATF	chr6:68159574-68159759	GM12878	blood:	n/a	n/a
7	BATF	chr6:68159560-68159863	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:68109011-68109057	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:68159661-68159872	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:68112393-68112571	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:68055825-68056288	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:68056059-68056095	GM12878	blood:	n/a	n/a
13	BRCA1	chr6:68073065-68073089	HepG2	liver:	n/a	n/a
14	CBX3	chr6:68055787-68056198	K562	blood:	n/a	n/a
15	CBX3	chr6:68168187-68168596	K562	blood:	n/a	n/a
16	CBX3	chr6:68072741-68073220	K562	blood:	n/a	n/a
17	CBX3	chr6:68168194-68168505	K562	blood:	n/a	n/a
18	CBX3	chr6:68104201-68104505	K562	blood:	n/a	n/a
19	CCNT2	chr6:68152042-68152242	K562	blood:	n/a	n/a
20	CCNT2	chr6:68079697-68079914	K562	blood:	n/a	chr6:68079717-68079737
21	CCNT2	chr6:68071129-68071190	K562	blood:	n/a	n/a
22	CCNT2	chr6:68143139-68143339	K562	blood:	n/a	n/a
23	CEBPB	chr6:68140017-68140312	K562	blood:	n/a	chr6:68140145-68140156
24	CEBPB	chr6:68058980-68059116	K562	blood:	n/a	chr6:68059044-68059057
25	CEBPB	chr6:68055874-68056182	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:68096675-68097112	A549	lung:	n/a	chr6:68096763-68096774
27	CEBPB	chr6:68101890-68102226	HepG2	liver:	n/a	chr6:68101934-68101947 chr6:68101934-68101947 chr6:68102053-68102066 chr6:68101936-68101947 chr6:68102053-68102064
28	CEBPB	chr6:68062637-68062967	A549	lung:	n/a	chr6:68062790-68062801
29	CEBPB	chr6:68078269-68078551	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:68143115-68143284	K562	blood:	n/a	chr6:68143228-68143239
31	CEBPB	chr6:68182534-68182752	A549	lung:	n/a	chr6:68182587-68182600 chr6:68182589-68182600 chr6:68182587-68182598 chr6:68182587-68182600
32	CEBPB	chr6:68072988-68073260	K562	blood:	n/a	chr6:68073141-68073154 chr6:68073141-68073152
33	CEBPB	chr6:68062620-68062983	HepG2	liver:	n/a	chr6:68062790-68062801
34	CEBPB	chr6:68149313-68149536	HepG2	liver:	n/a	chr6:68149429-68149440 chr6:68149429-68149442
35	CEBPB	chr6:68092161-68092438	IMR90	lung:	n/a	chr6:68092282-68092293 chr6:68092282-68092295 chr6:68092284-68092295 chr6:68092284-68092293 chr6:68092282-68092295
36	CEBPB	chr6:68072857-68073356	K562	blood:	n/a	chr6:68073141-68073154 chr6:68073141-68073152
37	CEBPB	chr6:68101796-68102249	Hela-S3	cervix:	n/a	chr6:68101934-68101947 chr6:68101934-68101947 chr6:68102053-68102066 chr6:68101936-68101947 chr6:68102053-68102064
38	CEBPB	chr6:68140021-68140300	IMR90	lung:	n/a	chr6:68140145-68140156
39	CEBPB	chr6:68092103-68092439	HepG2	liver:	n/a	chr6:68092282-68092293 chr6:68092282-68092295 chr6:68092284-68092295 chr6:68092284-68092293 chr6:68092282-68092295
40	CEBPB	chr6:68099666-68099744	K562	blood:	n/a	n/a
41	CEBPB	chr6:68092140-68092434	K562	blood:	n/a	chr6:68092282-68092293 chr6:68092282-68092295 chr6:68092284-68092295 chr6:68092284-68092293 chr6:68092282-68092295
42	CEBPB	chr6:68182476-68182771	HepG2	liver:	n/a	chr6:68182587-68182600 chr6:68182589-68182600 chr6:68182587-68182598 chr6:68182587-68182600
43	CEBPB	chr6:68143105-68143354	H1-hESC	embryonic stem cell:	n/a	chr6:68143228-68143239
44	CEBPB	chr6:68101891-68102205	K562	blood:	n/a	chr6:68101934-68101947 chr6:68101934-68101947 chr6:68102053-68102066 chr6:68101936-68101947 chr6:68102053-68102064
45	CEBPB	chr6:68084423-68084603	K562	blood:	n/a	n/a
46	CEBPB	chr6:68103151-68103385	HepG2	liver:	n/a	chr6:68103300-68103311 chr6:68103301-68103312
47	CEBPB	chr6:68182461-68182760	K562	blood:	n/a	chr6:68182587-68182600 chr6:68182589-68182600 chr6:68182587-68182598 chr6:68182587-68182600
48	CEBPB	chr6:68078311-68078543	A549	lung:	n/a	n/a
49	CEBPB	chr6:68043759-68043827	K562	blood:	n/a	chr6:68043780-68043791
50	CEBPB	chr6:68062672-68062951	K562	blood:	n/a	chr6:68062790-68062801

No.	Distal block	Cell Line	Cell type
1	chr6:68150563..68152778-chr6:68155646..68157250,2	K562	blood:
2	chr6:68077520..68081954-chr6:68082718..68085102,4	K562	blood:
3	chr6:68055450..68058632-chr6:68060210..68064044,3	MCF-7	breast:
4	chr6:68155527..68157923-chr6:68158676..68160978,2	K562	blood:
5	chr6:68184037..68187227-chr6:68190203..68192968,3	K562	blood:
6	chr6:68155527..68157923-chr6:68158676..68160978,2	K562	blood:
7	chr6:68047804..68050717-chr6:68052651..68054460,2	K562	blood:
8	chr6:68148937..68151078-chr6:68174672..68177614,2	K562	blood:
9	chr6:68047804..68050717-chr6:68052651..68054460,2	K562	blood:
10	chr6:68036021..68038147-chr6:68069085..68071759,2	K562	blood:
11	chr6:68130955..68133450-chr6:68149900..68151602,2	MCF-7	breast:
12	chr6:68170096..68172631-chr6:68173230..68175635,2	K562	blood:
13	chr6:68028783..68032532-chr6:68036632..68039695,4	K562	blood:
14	chr6:68075451..68077006-chr6:68082097..68085010,2	K562	blood:
15	chr6:68100365..68102401-chr6:68111000..68113004,2	K562	blood:
16	chr6:68117073..68119552-chr6:68122982..68124774,2	MCF-7	breast:
17	chr6:68029025..68030581-chr6:68070322..68071978,2	K562	blood:
18	chr6:68148314..68150953-chr6:68152002..68154440,2	K562	blood:
19	chr6:68105788..68108558-chr6:68122131..68123769,2	K562	blood:
20	chr6:68148314..68150953-chr6:68152002..68154440,2	K562	blood:
21	chr6:68161779..68164395-chr6:68176566..68178656,2	K562	blood:
22	chr6:68116391..68119187-chr6:68123257..68125394,2	K562	blood:
23	chr6:68026494..68028999-chr6:68072957..68074504,2	K562	blood:
24	chr6:68099897..68102194-chr6:68105769..68107802,2	K562	blood:
25	chr6:68149200..68150953-chr6:68151779..68154440,2	K562	blood:
26	chr6:67641579..67644100-chr6:68068975..68070914,2	K562	blood:
27	chr3:40565910..40566852-chr6:68076614..68077483,2	MCF-7	breast:
28	chr6:68055450..68058632-chr6:68060210..68064044,3	MCF-7	breast:
29	chr6:68151435..68153326-chr6:68157000..68158589,2	MCF-7	breast:
30	chr6:68170096..68172631-chr6:68173230..68175635,2	K562	blood:
31	chr6:68166848..68170482-chr6:68173830..68176877,3	K562	blood:
32	chr6:68151435..68153326-chr6:68157000..68158589,2	MCF-7	breast:
33	chr6:68061490..68063825-chr6:68066626..68069282,2	K562	blood:
34	chr6:68062325..68064771-chr6:68066321..68068609,3	K562	blood:
35	chr6:68116391..68119187-chr6:68123257..68125394,2	K562	blood:
36	chr6:68085152..68088022-chr6:68089241..68092194,2	MCF-7	breast:
37	chr6:68117073..68119552-chr6:68122982..68124774,2	MCF-7	breast:
38	chr6:68062325..68064771-chr6:68066321..68068609,3	K562	blood:
39	chr22:36852253..36854026-chr6:68056023..68057523,2	K562	blood:
40	chr6:68142298..68144870-chr6:68147425..68149399,2	K562	blood:
41	chr6:68036021..68038147-chr6:68069085..68071759,2	K562	blood:
42	chr6:68075451..68077006-chr6:68082097..68085010,2	K562	blood:
43	chr6:68061490..68063825-chr6:68066626..68069282,2	K562	blood:
44	chr6:68117687..68119606-chr6:68122416..68125394,2	K562	blood:
45	chr6:68117687..68119606-chr6:68122416..68125394,2	K562	blood:
46	chr6:68099897..68102194-chr6:68105769..68107802,2	K562	blood:
47	chr6:68149200..68150953-chr6:68151779..68154440,2	K562	blood:
48	chr6:68153475..68156180-chr6:68165524..68167480,2	K562	blood:
49	chr14:90865957..90866488-chr6:68144436..68144955,2	MCF-7	breast:
50	chr6:68077520..68081954-chr6:68082718..68085102,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL713998.1-5	chr6:68166239-68167143	NONHSAT113387
2	lnc-BAI3-8	chr6:68172696-68172760	NONHSAT113386
3	lnc-BAI3-4	chr6:68095844-68095887	XLOC_005337
4	lnc-BAI3-8	chr6:68162493-68162620	NONHSAT113386
5	lnc-BAI3-4	chr6:68095954-68096267	XLOC_005337
6	lnc-BAI3-8	chr6:68169681-68171236	NONHSAT113386
7	lnc-BAI3-8	chr6:68172396-68172434	NONHSAT113386

Variant related genes	Relation type
ENSG00000271111	TF binding region
RNA5SP208	TF binding region
ENSG00000271111	chromatin interactions
ENSG00000251965	chromatin interactions
ENSG00000198668	chromatin interactions
ENSG00000172888	chromatin interactions
EIF2A	miRNA target sites
LRRFIP1	miRNA target sites

Extended variants
information (count: 1667 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1667 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13201396	chr6:68033877-68033878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545366263	chr6:68034047-68034048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35606832	chr6:68034067-68034068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs397885738	chr6:68034068-68034069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143651360	chr6:68034097-68034098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34785546	chr6:68034110-68034111	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs78247795	chr6:68034138-68034139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs36032174	chr6:68034172-68034173	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs148076445	chr6:68034195-68034196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114848148	chr6:68034219-68034220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192959964	chr6:68034220-68034221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544160068	chr6:68034239-68034240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563437639	chr6:68034281-68034282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532406444	chr6:68034282-68034283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552099814	chr6:68034301-68034302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559532477	chr6:68034316-68034317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34963995	chr6:68034318-68034319	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs34977905	chr6:68034324-68034325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs182792106	chr6:68034332-68034333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112408668	chr6:68034387-68034388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573136698	chr6:68034435-68034436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576272550	chr6:68034440-68034441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35679777	chr6:68034460-68034461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397886147	chr6:68034462-68034463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200070419	chr6:68034468-68034469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9351657	chr6:68034473-68034474	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs138843820	chr6:68034489-68034490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142796673	chr6:68034498-68034499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540161419	chr6:68034507-68034508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553369439	chr6:68034523-68034524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188701269	chr6:68034529-68034530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192984930	chr6:68034530-68034531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147385874	chr6:68034552-68034553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575287110	chr6:68034573-68034574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544219264	chr6:68034587-68034588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139553115	chr6:68034598-68034599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35323449	chr6:68034618-68034619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149467805	chr6:68034628-68034629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546104008	chr6:68034630-68034631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184324314	chr6:68034638-68034639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189434157	chr6:68034639-68034640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542001460	chr6:68034652-68034653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561790681	chr6:68034728-68034729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192431771	chr6:68034751-68034752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78571181	chr6:68034844-68034845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183666311	chr6:68034846-68034847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs578109214	chr6:68034885-68034886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545564627	chr6:68034980-68034981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34249322	chr6:68034989-68034990	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs112773491	chr6:68035005-68035006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:68030400-68035600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:68037800-68038200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:68040600-68041200	Enhancers	Fetal Brain Male	brain
4	chr6:68041200-68041600	Weak transcription	Fetal Brain Male	brain
5	chr6:68041600-68042000	Enhancers	Fetal Brain Male	brain
6	chr6:68050200-68050600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:68050600-68054000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:68054000-68054400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr6:68055600-68056600	Enhancers	HMEC	breast
10	chr6:68055600-68056600	Enhancers	NHEK	skin
11	chr6:68055800-68056400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:68056000-68056400	Enhancers	HepG2	liver
13	chr6:68056200-68056600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:68062800-68064200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr6:68063000-68064400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:68063600-68064400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:68068200-68068800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr6:68068200-68069400	Enhancers	K562	blood
19	chr6:68068800-68071000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:68069400-68071000	Weak transcription	K562	blood
21	chr6:68070800-68071000	Enhancers	HepG2	liver
22	chr6:68070800-68071400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:68071000-68071200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr6:68071000-68071200	Enhancers	Dnd41	blood
25	chr6:68071000-68071200	Flanking Active TSS	K562	blood
26	chr6:68071000-68071400	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr6:68071000-68071400	Flanking Active TSS	HepG2	liver
28	chr6:68071000-68071600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr6:68071000-68071600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:68071200-68071400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:68071200-68071400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:68071200-68071600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr6:68071200-68071600	Flanking Active TSS	Dnd41	blood
34	chr6:68071200-68071800	Active TSS	A549	lung
35	chr6:68071200-68073800	Active TSS	K562	blood
36	chr6:68071400-68071800	Active TSS	HepG2	liver
37	chr6:68071600-68072000	Enhancers	Dnd41	blood
38	chr6:68073800-68074000	Flanking Active TSS	K562	blood
39	chr6:68094200-68095000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:68108400-68109000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr6:68112200-68112600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:68112400-68112600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr6:68120800-68121400	Enhancers	HUVEC	blood vessel
44	chr6:68121000-68121400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:68143200-68143600	Enhancers	K562	blood
46	chr6:68156000-68156600	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr6:68159400-68159800	Enhancers	Fetal Heart	heart
48	chr6:68159800-68163000	Weak transcription	Fetal Heart	heart
49	chr6:68163000-68163400	Enhancers	Fetal Heart	heart
50	chr6:68167600-68168600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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