Variant report

Variant	esv3430800
Chromosome Location	chr4:2961729-2964002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:155)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:155 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:2963128-2963328	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:2963866-2964220	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:2962087-2962384	HepG2	liver:	n/a	n/a
4	BATF	chr4:2963779-2964111	GM12878	blood:	n/a	n/a
5	BATF	chr4:2963732-2964116	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:2963194-2963383	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:2962145-2962326	K562	blood:	n/a	n/a
8	CEBPB	chr4:2963492-2963904	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr4:2963290-2963449	K562	blood:	n/a	n/a
10	CTCF	chr4:2963760-2963910	HEK293	kidney:	n/a	n/a
11	CTCF	chr4:2963840-2963990	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr4:2963520-2963670	GM12878	blood:	n/a	n/a
13	CTCF	chr4:2963780-2963930	GM12872	blood:	n/a	n/a
14	CTCF	chr4:2963840-2963990	GM12878	blood:	n/a	n/a
15	CTCF	chr4:2963820-2963970	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr4:2963800-2963950	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr4:2963840-2963990	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr4:2963800-2963950	GM12874	blood:	n/a	n/a
19	CTCF	chr4:2963760-2963910	GM12864	blood:	n/a	n/a
20	CTCF	chr4:2963893-2963943	GM13976	blood:	n/a	n/a
21	CTCF	chr4:2963760-2963910	GM12866	blood:	n/a	n/a
22	CTCF	chr4:2963660-2963810	HVMF	connective:	n/a	n/a
23	CTCF	chr4:2963620-2963770	HAc	cerebellar:	n/a	n/a
24	CTCF	chr4:2963740-2963890	GM06990	blood:	n/a	n/a
25	CTCF	chr4:2963845-2963904	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr4:2963800-2963950	GM12873	blood:	n/a	n/a
27	CTCF	chr4:2963840-2963990	GM12869	blood:	n/a	n/a
28	CTCF	chr4:2963760-2963910	HMF	breast:	n/a	n/a
29	CTCF	chr4:2963820-2963970	K562	blood:	n/a	n/a
30	CTCF	chr4:2963810-2963927	GM12878	blood:	n/a	n/a
31	CTCF	chr4:2963540-2963690	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:2963780-2963930	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr4:2963861-2963949	GM10248	blood:	n/a	n/a
34	CTCF	chr4:2963800-2963950	AG10803	skin:	n/a	n/a
35	CTCF	chr4:2963800-2963950	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr4:2963900-2964050	GM12864	blood:	n/a	n/a
37	CTCF	chr4:2963620-2963910	HCFaa	heart:	n/a	n/a
38	CTCF	chr4:2963780-2963930	AG10803	skin:	n/a	n/a
39	CTCF	chr4:2963800-2963950	BJ	skin:	n/a	n/a
40	CTCF	chr4:2963800-2963950	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr4:2963780-2963930	GM12867	blood:	n/a	n/a
42	CTCF	chr4:2963480-2963630	AG04449	skin:	n/a	n/a
43	CTCF	chr4:2963760-2963910	AG04449	skin:	n/a	n/a
44	CTCF	chr4:2963820-2963970	GM12865	blood:	n/a	n/a
45	CTCF	chr4:2963725-2964062	GM12878	blood:	n/a	n/a
46	CTCF	chr4:2963800-2963950	GM12870	blood:	n/a	n/a
47	CTCF	chr4:2963720-2963870	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr4:2963780-2963930	AG04450	lung:	n/a	n/a
49	CTCF	chr4:2963880-2964030	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:2963700-2963850	BE2_C	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2963264-2963314	GM12878	blood:	n/a
2	chr4:2963261-2963311	BJ	skin:	n/a
3	chr4:2963264-2963314	BJ	skin:	n/a
4	chr4:2963261-2963311	HCT-116	colon:	n/a
5	chr4:2963264-2963314	HIPEpiC	eye:	n/a
6	chr4:2963264-2963314	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:2963261-2963311	MCF-7	breast:	n/a
8	chr4:2963261-2963311	LNCaP	prostate:	n/a
9	chr4:2963261-2963311	NHBE	bronchial:	n/a
10	chr4:2963261-2963311	PFSK-1	brain:	n/a
11	chr4:2963261-2963311	HRCEpiC	kidney:	n/a
12	chr4:2963264-2963314	AG09319	gingival:	n/a
13	chr4:2963264-2963314	GM12891	blood:	n/a
14	chr4:2963261-2963311	Hela-S3	cervix:	n/a
15	chr4:2963264-2963314	GM06990	blood:	n/a
16	chr4:2963261-2963311	GM12892	blood:	n/a
17	chr4:2963264-2963314	HRE	kidney:	n/a
18	chr4:2963264-2963314	HL-60	blood:	n/a
19	chr4:2963261-2963311	HL-60	blood:	n/a
20	chr4:2963264-2963314	U87	brain:	n/a
21	chr4:2963261-2963311	SKMC	muscle:	n/a
22	chr4:2963261-2963311	SK-N-MC	brain:	n/a
23	chr4:2963261-2963311	GM06990	blood:	n/a
24	chr4:2963264-2963314	HMEC	breast:	n/a
25	chr4:2963261-2963311	Caco-2	colon:	n/a
26	chr4:2963264-2963314	HCF	heart:	n/a
27	chr4:2963264-2963314	AoSMC	blood vessel:	n/a
28	chr4:2963261-2963311	HepG2	liver:	n/a
29	chr4:2963264-2963314	Caco-2	colon:	n/a
30	chr4:2963264-2963314	HCPEpiC	choroid plexus:	n/a
31	chr4:2963264-2963314	ovcar-3	ovarian:	n/a
32	chr4:2963261-2963311	AG09319	gingival:	n/a
33	chr4:2963264-2963314	MCF10A-Er-Src	breast:	n/a
34	chr4:2963264-2963314	SK-N-MC	brain:	n/a
35	chr4:2963261-2963311	U87	brain:	n/a
36	chr4:2963261-2963311	BE2_C	brain:	n/a
37	chr4:2963264-2963314	HNPCEpiC	eye:	n/a
38	chr4:2963264-2963314	Jurkat	blood:	n/a
39	chr4:2963264-2963314	AG10803	skin:	n/a
40	chr4:2963264-2963314	GM19239	blood:	n/a
41	chr4:2963261-2963311	GM19239	blood:	n/a
42	chr4:2963264-2963314	ProgFib	skin:	n/a
43	chr4:2963261-2963311	NH-A	brain:	n/a
44	chr4:2963264-2963314	LNCaP	prostate:	n/a
45	chr4:2963261-2963311	SK-N-SH	brain:	n/a
46	chr4:2963261-2963311	HAEpiC	amniotic membrane:	n/a
47	chr4:2963264-2963314	Hela-S3	cervix:	n/a
48	chr4:2963264-2963314	ECC-1	luminal epithelium:	n/a
49	chr4:2963264-2963314	PANC-1	pancreas:	n/a
50	chr4:2963261-2963311	ovcar-3	ovarian:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2756517..2759780-chr4:2963075..2966456,5	K562	blood:
2	chr4:2961872..2963731-chr4:3064483..3066913,2	K562	blood:
3	chr4:2756517..2759604-chr4:2963075..2966301,5	K562	blood:
4	chr4:2948727..2950755-chr4:2959506..2963214,4	K562	blood:
5	chr4:2936328..2940860-chr4:2961848..2966602,8	K562	blood:
6	chr4:2959980..2962211-chr4:2969909..2971816,3	MCF-7	breast:
7	chr4:2916201..2917764-chr4:2963610..2965346,2	K562	blood:
8	chr4:2845175..2847151-chr4:2963481..2966387,2	MCF-7	breast:
9	chr4:2948388..2950164-chr4:2962609..2964597,2	MCF-7	breast:
10	chr4:2963799..2967429-chr4:2967585..2973552,6	K562	blood:
11	chr4:1857657..1859808-chr4:2963800..2965708,2	MCF-7	breast:
12	chr4:2963409..2964972-chr4:2976613..2978274,2	MCF-7	breast:
13	chr4:2960088..2962960-chr4:3074155..3076323,2	MCF-7	breast:
14	chr4:2937577..2939558-chr4:2961657..2964358,2	MCF-7	breast:
15	chr4:2795940..2798085-chr4:2962031..2964351,2	MCF-7	breast:
16	chr4:2935142..2937747-chr4:2962615..2966345,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADD1-1	chr4:2963081-2963465	ENSG00000249673

No data

Variant related genes	Relation type
GRK4	TF binding region
GRK4	CpG island
ENSG00000109736	chromatin interactions
ENSG00000251075	chromatin interactions
ENSG00000249673	chromatin interactions
ENSG00000087274	chromatin interactions
ENSG00000125388	chromatin interactions
ENSG00000168884	chromatin interactions
ENSG00000168924	chromatin interactions
PABPC4	miRNA target sites

Extended variants
information (count: 157 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:157 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541418719	chr4:2961735-2961736	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs561836072	chr4:2961774-2961775	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs1269355	chr4:2961783-2961784	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs547288508	chr4:2961785-2961786	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs570599873	chr4:2961787-2961788	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs146131984	chr4:2961791-2961792	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs550334376	chr4:2961797-2961798	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs570157668	chr4:2961800-2961801	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs535898839	chr4:2961821-2961822	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs555687786	chr4:2961822-2961823	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs6836526	chr4:2961827-2961828	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs535296398	chr4:2961834-2961835	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs558144822	chr4:2961842-2961843	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs367588520	chr4:2961886-2961887	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs143916827	chr4:2961898-2961899	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs543599895	chr4:2961919-2961920	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs555884970	chr4:2961936-2961937	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs186976589	chr4:2961967-2961968	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs192698532	chr4:2961998-2961999	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs561689539	chr4:2962005-2962006	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs527613988	chr4:2962022-2962023	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs146656983	chr4:2962033-2962034	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs77732524	chr4:2962069-2962070	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs533206344	chr4:2962077-2962078	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs35120496	chr4:2962091-2962092	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs549997938	chr4:2962134-2962135	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs372381427	chr4:2962182-2962183	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs570166282	chr4:2962188-2962189	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs376781734	chr4:2962200-2962201	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs549126493	chr4:2962215-2962216	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs111447144	chr4:2962250-2962251	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs534693029	chr4:2962264-2962265	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs185693171	chr4:2962322-2962323	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs571604625	chr4:2962352-2962353	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs537248753	chr4:2962385-2962386	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs554790253	chr4:2962387-2962388	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs201789208	chr4:2962390-2962391	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs188972117	chr4:2962393-2962394	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs535504733	chr4:2962395-2962396	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs193045879	chr4:2962403-2962404	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs572043942	chr4:2962408-2962409	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs369723482	chr4:2962415-2962416	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs9686032	chr4:2962421-2962422	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
44	rs184392633	chr4:2962422-2962423	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs34508820	chr4:2962425-2962426	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs150954762	chr4:2962432-2962433	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
47	rs188780457	chr4:2962438-2962439	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs35681707	chr4:2962452-2962453	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
49	rs60925145	chr4:2962469-2962470	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs189326415	chr4:2962477-2962478	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
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
Developmental delay	21147756	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
Breast cancer	22522925	CNVD
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2938200-2962200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:2938400-2962200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr4:2939200-2963200	Weak transcription	Fetal Heart	heart
4	chr4:2939400-2962200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr4:2940000-2962200	Strong transcription	Primary B cells from peripheral blood	blood
6	chr4:2948800-2963200	Strong transcription	Fetal Intestine Small	intestine
7	chr4:2953600-2963200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr4:2954400-2962400	Strong transcription	A549	lung
9	chr4:2956000-2963200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:2957600-2961800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr4:2957600-2962200	Strong transcription	Fetal Intestine Large	intestine
12	chr4:2958200-2962200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:2958200-2963200	Weak transcription	Stomach Mucosa	stomach
14	chr4:2958400-2963000	Strong transcription	K562	blood
15	chr4:2958400-2963200	Weak transcription	Brain Substantia Nigra	brain
16	chr4:2958400-2963200	Weak transcription	Fetal Brain Male	brain
17	chr4:2958400-2963200	Weak transcription	Fetal Kidney	kidney
18	chr4:2958600-2962400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr4:2958800-2963200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:2958800-2963200	Weak transcription	Colon Smooth Muscle	Colon
21	chr4:2959200-2962600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr4:2959200-2963000	Weak transcription	Brain Germinal Matrix	brain
23	chr4:2959200-2964400	Weak transcription	Aorta	Aorta
24	chr4:2959400-2962000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr4:2959400-2963000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr4:2959400-2963000	Weak transcription	Pancreas	Pancrea
27	chr4:2959400-2963000	Weak transcription	Small Intestine	intestine
28	chr4:2959400-2963200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr4:2959400-2963600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr4:2959600-2963000	Weak transcription	Brain Anterior Caudate	brain
31	chr4:2959600-2963000	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr4:2959600-2963200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr4:2959600-2963200	Weak transcription	Colonic Mucosa	Colon
34	chr4:2959800-2961800	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr4:2959800-2963000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr4:2959800-2963200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr4:2959800-2963200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:2959800-2963200	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr4:2959800-2963200	Weak transcription	Rectal Smooth Muscle	rectum
40	chr4:2959800-2963400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr4:2960000-2963000	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr4:2960000-2963200	Weak transcription	Brain Angular Gyrus	brain
43	chr4:2960000-2963200	Weak transcription	Esophagus	oesophagus
44	chr4:2960200-2962200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:2960200-2962200	Genic enhancers	Primary T cells fromperipheralblood	blood
46	chr4:2960400-2962400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:2960400-2963200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:2960400-2963200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr4:2960400-2963200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr4:2960600-2962200	Genic enhancers	Primary T helper cells PMA-I stimulated	--

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