Variant report

Variant	nsv527542
Chromosome Location	chr21:48015869-48027880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:111)
CpG islands
(count:917)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:111 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr21:48017955-48018252	K562	blood:	n/a	chr21:48018068-48018088
2	BCLAF1	chr21:48025984-48026402	GM12878	blood:	n/a	n/a
3	CBX3	chr21:48017809-48018333	K562	blood:	n/a	n/a
4	CBX3	chr21:48017920-48018249	K562	blood:	n/a	n/a
5	CEBPB	chr21:48020264-48020558	K562	blood:	n/a	n/a
6	CTCF	chr21:48018165-48018252	K562	blood:	n/a	chr21:48018186-48018199
7	CTCF	chr21:48018100-48018250	GM12867	blood:	n/a	chr21:48018186-48018199
8	CTCF	chr21:48018020-48018170	K562	blood:	n/a	n/a
9	CTCF	chr21:48018049-48018377	K562	blood:	n/a	chr21:48018186-48018199
10	CTCF	chr21:48018060-48018210	Hela-S3	cervix:	n/a	chr21:48018186-48018199
11	CTCF	chr21:48018080-48018230	K562	blood:	n/a	chr21:48018186-48018199
12	CTCF	chr21:48018048-48018372	K562	blood:	n/a	chr21:48018186-48018199
13	CTCF	chr21:48018005-48018273	K562	blood:	n/a	chr21:48018186-48018199
14	EBF1	chr21:48025973-48026546	GM12878	blood:	n/a	n/a
15	EBF1	chr21:48026020-48026423	GM12878	blood:	n/a	n/a
16	EGR1	chr21:48018008-48018258	K562	blood:	n/a	chr21:48018193-48018206
17	EGR1	chr21:48024963-48025225	K562	blood:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
18	EGR1	chr21:48024900-48025237	H1-hESC	embryonic stem cell:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
19	EGR1	chr21:48018016-48018248	K562	blood:	n/a	chr21:48018193-48018206
20	EGR1	chr21:48024866-48025287	ECC-1	luminal epithelium:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
21	EGR1	chr21:48024950-48025231	K562	blood:	n/a	chr21:48025215-48025224 chr21:48025099-48025108 chr21:48025096-48025109
22	ELF1	chr21:48017731-48018266	K562	blood:	n/a	chr21:48017927-48017938
23	ELF1	chr21:48017729-48017997	K562	blood:	n/a	chr21:48017927-48017938
24	ELF1	chr21:48026001-48026710	GM12878	blood:	n/a	chr21:48026169-48026182
25	ELF1	chr21:48025991-48026352	K562	blood:	n/a	chr21:48026169-48026182
26	ELF1	chr21:48024860-48025163	GM12878	blood:	n/a	n/a
27	ELF1	chr21:48018047-48018261	K562	blood:	n/a	n/a
28	ELF1	chr21:48017829-48018255	GM12878	blood:	n/a	chr21:48017927-48017938
29	FOXA1	chr21:48019127-48019628	HepG2	liver:	n/a	n/a
30	FOXA1	chr21:48019136-48019530	HepG2	liver:	n/a	n/a
31	FOXA2	chr21:48019170-48019497	HepG2	liver:	n/a	n/a
32	FOXA2	chr21:48021843-48022079	HepG2	liver:	n/a	n/a
33	FOXP2	chr21:48025023-48025439	SK-N-MC	brain:	n/a	n/a
34	GABPA	chr21:48017964-48018293	K562	blood:	n/a	n/a
35	MAX	chr21:48019057-48019520	HepG2	liver:	n/a	n/a
36	MAX	chr21:48017880-48018264	K562	blood:	n/a	chr21:48018067-48018078 chr21:48018068-48018077
37	MAX	chr21:48018973-48019538	SK-N-SH	brain:	n/a	n/a
38	MTA3	chr21:48025902-48026524	GM12878	blood:	n/a	n/a
39	MXI1	chr21:48018937-48019784	SK-N-SH	brain:	n/a	n/a
40	MXI1	chr21:48018875-48019723	IMR90	lung:	n/a	n/a
41	MYC	chr21:48019097-48019546	HUVEC	blood vessel:	n/a	n/a
42	PAX5	chr21:48026004-48026350	GM12878	blood:	n/a	n/a
43	PAX5	chr21:48025886-48026416	GM12878	blood:	n/a	n/a
44	POLR2A	chr21:48026198-48026201	MCF-7	breast:	n/a	n/a
45	POLR2A	chr21:48026255-48026292	MCF-7	breast:	n/a	n/a
46	POLR2A	chr21:48021365-48021492	GM12878	blood:	n/a	n/a
47	POLR2A	chr21:48016573-48017473	SK-N-MC	brain:	n/a	n/a
48	POLR2A	chr21:48019041-48019098	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr21:48017980-48018076	K562	blood:	n/a	n/a
50	POLR2A	chr21:48017978-48017992	MCF-7	breast:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:48018790-48018840	HUVEC	blood vessel:	n/a
2	chr21:48019296-48019346	PFSK-1	brain:	n/a
3	chr21:48018790-48018840	HUVEC	blood vessel:	n/a
4	chr21:48019296-48019346	PFSK-1	brain:	n/a
5	chr21:48022339-48022389	GM12891	blood:	n/a
6	chr21:48018790-48018840	IMR90	lung:	fetal
7	chr21:48018608-48018658	AG09319	gingival:	n/a
8	chr21:48026181-48026231	HRPEpiC	eye:	n/a
9	chr21:48021941-48021991	MCF10A-Er-Src	breast:	n/a
10	chr21:48025691-48025741	GM19239	blood:	n/a
11	chr21:48018790-48018840	NT2-D1	testis:	n/a
12	chr21:48026181-48026231	SK-N-SH	brain:	n/a
13	chr21:48024639-48024689	MCF-7	breast:	n/a
14	chr21:48018608-48018658	IMR90	lung:	fetal
15	chr21:48026043-48026093	HMEC	breast:	n/a
16	chr21:48017232-48017282	HL-60	blood:	n/a
17	chr21:48018790-48018840	AoSMC	blood vessel:	n/a
18	chr21:48025100-48025150	AG09309	skin:	n/a
19	chr21:48025691-48025741	H1-hESC	embryonic stem cell:	embryo
20	chr21:48025155-48025205	AoSMC	blood vessel:	n/a
21	chr21:48017232-48017282	GM12878	blood:	n/a
22	chr21:48025100-48025150	AG10803	skin:	n/a
23	chr21:48021941-48021991	SK-N-SH_RA	brain:	n/a
24	chr21:48025100-48025150	ECC-1	luminal epithelium:	n/a
25	chr21:48022339-48022389	SK-N-SH_RA	brain:	n/a
26	chr21:48026298-48026348	U87	brain:	n/a
27	chr21:48018608-48018658	K562	blood:	n/a
28	chr21:48018790-48018840	HRCEpiC	kidney:	n/a
29	chr21:48019296-48019346	SAEC	small airway:	n/a
30	chr21:48026298-48026348	HepG2	liver:	n/a
31	chr21:48021941-48021991	HCT-116	colon:	n/a
32	chr21:48025100-48025150	HEK293	kidney:	embryo
33	chr21:48018790-48018840	HEK293	kidney:	embryo
34	chr21:48026043-48026093	ovcar-3	ovarian:	n/a
35	chr21:48018790-48018840	AG09319	gingival:	n/a
36	chr21:48018790-48018840	HCM	heart:	n/a
37	chr21:48021941-48021991	NH-A	brain:	n/a
38	chr21:48022339-48022389	NT2-D1	testis:	n/a
39	chr21:48018790-48018840	ProgFib	skin:	n/a
40	chr21:48025155-48025205	HAEpiC	amniotic membrane:	n/a
41	chr21:48022339-48022389	T-47D	breast:	n/a
42	chr21:48017232-48017282	NH-A	brain:	n/a
43	chr21:48026298-48026348	HAEpiC	amniotic membrane:	n/a
44	chr21:48025691-48025741	HepG2	liver:	n/a
45	chr21:48018632-48018682	Caco-2	colon:	n/a
46	chr21:48018632-48018682	HNPCEpiC	eye:	n/a
47	chr21:48025691-48025741	NHDF-neo	bronchial:	n/a
48	chr21:48018608-48018658	H1-hESC	embryonic stem cell:	embryo
49	chr21:48018790-48018840	AG10803	skin:	n/a
50	chr21:48018790-48018840	CMK	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:48016127..48018173-chr21:48020936..48022713,2	K562	blood:
2	chr21:48021498..48023722-chr21:48025363..48027869,3	K562	blood:
3	chr21:48013557..48016686-chr21:48017781..48019868,3	MCF-7	breast:
4	chr21:48017805..48022026-chr21:48053687..48056894,4	K562	blood:
5	chr21:48016127..48018173-chr21:48020936..48022713,2	K562	blood:
6	chr21:48017941..48023722-chr21:48025363..48028133,5	K562	blood:
7	chr21:48016422..48019126-chr21:48030129..48032645,2	K562	blood:
8	chr21:48027694..48030453-chr21:48039157..48041006,2	MCF-7	breast:
9	chr21:48019242..48021637-chr21:48023777..48026826,3	MCF-7	breast:
10	chr21:48025522..48028149-chr21:48060514..48063166,2	MCF-7	breast:
11	chr21:47986444..47988898-chr21:48015731..48017367,2	K562	blood:
12	chr21:48024575..48027546-chr21:48055306..48056858,2	K562	blood:
13	chr21:48013557..48016686-chr21:48017781..48019868,3	MCF-7	breast:
14	chr21:48025603..48028303-chr21:48029330..48031658,3	MCF-7	breast:
15	chr21:48021540..48023901-chr21:48055495..48057109,2	MCF-7	breast:
16	chr21:47980753..47982887-chr21:48026648..48028879,2	MCF-7	breast:
17	chr21:48023339..48026982-chr21:48053855..48056881,6	MCF-7	breast:
18	chr21:47920604..47922605-chr21:48015742..48017826,2	K562	blood:

No data

Variant related genes	Relation type
S100B	TF binding region
S100B	CpG island
ENSG00000160305	chromatin interactions
ENSG00000160307	chromatin interactions
ENSG00000160310	chromatin interactions

Extended variants
information (count: 515 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:515 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839343	chr21:48015869-48015870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148008615	chr21:48015876-48015877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537411560	chr21:48015886-48015887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558651437	chr21:48015913-48015914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555499060	chr21:48015938-48015939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147436409	chr21:48015972-48015973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184351011	chr21:48016058-48016059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs386819457	chr21:48016067-48016068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs59220795	chr21:48016068-48016069	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs112345771	chr21:48016069-48016070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376496789	chr21:48016070-48016071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183963065	chr21:48016091-48016092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536880313	chr21:48016110-48016111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189367046	chr21:48016169-48016170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575185578	chr21:48016293-48016294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs59454503	chr21:48016326-48016327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542578321	chr21:48016350-48016351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79527268	chr21:48016408-48016409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575034694	chr21:48016415-48016416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76359771	chr21:48016422-48016423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540963796	chr21:48016423-48016424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180741147	chr21:48016472-48016473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9974426	chr21:48016477-48016478	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs186652607	chr21:48016497-48016498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373930839	chr21:48016500-48016501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572824780	chr21:48016506-48016507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139176151	chr21:48016516-48016517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35657740	chr21:48016559-48016560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544992911	chr21:48016578-48016579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs16979449	chr21:48016605-48016606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs13046595	chr21:48016641-48016642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567544276	chr21:48016646-48016647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73907532	chr21:48016670-48016671	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs190999058	chr21:48016690-48016691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2839344	chr21:48016691-48016692	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs538414685	chr21:48016695-48016696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181577451	chr21:48016710-48016711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544424018	chr21:48016735-48016736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2839345	chr21:48016737-48016738	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs13050390	chr21:48016739-48016740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs13050395	chr21:48016742-48016743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2839346	chr21:48016748-48016749	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs561274351	chr21:48016772-48016773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529479275	chr21:48016829-48016830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572745277	chr21:48016833-48016834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546904035	chr21:48016847-48016848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs28524577	chr21:48016855-48016856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2839347	chr21:48016948-48016949	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs373361301	chr21:48017011-48017012	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77739211	chr21:48017017-48017018	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:48006000-48018600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr21:48013600-48018800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr21:48014000-48018600	Weak transcription	Primary T cells from cord blood	blood
4	chr21:48014400-48018000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr21:48014600-48018600	Weak transcription	Brain Anterior Caudate	brain
6	chr21:48014800-48017600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr21:48015200-48016200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr21:48015200-48017800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr21:48015200-48018600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr21:48015600-48016000	Enhancers	Brain Hippocampus Middle	brain
11	chr21:48015800-48016600	Enhancers	Brain Substantia Nigra	brain
12	chr21:48015800-48018600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr21:48016000-48016800	Enhancers	Fetal Muscle Leg	muscle
14	chr21:48016000-48016800	Enhancers	HepG2	liver
15	chr21:48016000-48018600	Weak transcription	Brain Hippocampus Middle	brain
16	chr21:48016200-48016600	Enhancers	Fetal Muscle Trunk	muscle
17	chr21:48016200-48017400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr21:48016400-48016600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr21:48016600-48018000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr21:48016600-48018600	Weak transcription	Brain Substantia Nigra	brain
21	chr21:48016800-48018600	Weak transcription	Fetal Muscle Leg	muscle
22	chr21:48016800-48018600	Weak transcription	HepG2	liver
23	chr21:48017000-48018400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr21:48017200-48017600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr21:48017200-48017600	Enhancers	Osteobl	bone
26	chr21:48017400-48017800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr21:48017400-48019400	Enhancers	Primary T cells fromperipheralblood	blood
28	chr21:48017600-48017800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr21:48017600-48017800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr21:48017600-48018600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr21:48017600-48018600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr21:48017600-48018800	Weak transcription	Osteobl	bone
33	chr21:48017600-48020200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr21:48017800-48018000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr21:48017800-48018000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr21:48017800-48018000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr21:48017800-48018000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr21:48017800-48018000	Enhancers	Gastric	stomach
39	chr21:48017800-48018000	Enhancers	Spleen	Spleen
40	chr21:48017800-48018200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
41	chr21:48017800-48018600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr21:48017800-48018800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr21:48017800-48019200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr21:48017800-48019400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr21:48017800-48020800	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr21:48018000-48018200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr21:48018000-48018200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr21:48018000-48018400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr21:48018000-48018600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr21:48018000-48019000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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