Variant report

Variant	esv3430608
Chromosome Location	chr1:228603354-228605902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:190)
CpG islands
(count:732)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:190 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:228603651-228604322	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr1:228604229-228604266	K562	blood:	n/a	n/a
3	CHD1	chr1:228603938-228604183	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr1:228604078-228604198	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr1:228604060-228604210	BJ	skin:	n/a	n/a
6	CTCF	chr1:228603966-228604033	Lung_OC	lung:	n/a	n/a
7	CTCF	chr1:228603995-228604127	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr1:228603940-228604090	HRE	kidney:	n/a	n/a
9	CTCF	chr1:228603980-228604130	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr1:228603980-228604130	SAEC	small airway:	n/a	n/a
11	CTCF	chr1:228603960-228604110	GM12864	blood:	n/a	n/a
12	CTCF	chr1:228603900-228604050	AG09309	skin:	n/a	n/a
13	CTCF	chr1:228604030-228604141	GM10266	blood:	n/a	n/a
14	CTCF	chr1:228603960-228604110	HCM	heart:	n/a	n/a
15	CTCF	chr1:228604246-228604247	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:228603599-228603601	GM19239	blood:	n/a	n/a
17	CTCF	chr1:228603861-228604242	IMR90	lung:	n/a	chr1:228604197-228604218
18	CTCF	chr1:228603912-228604271	H1-hESC	embryonic stem cell:	n/a	chr1:228604197-228604218
19	CTCF	chr1:228603960-228604110	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr1:228604000-228604150	HMEC	breast:	n/a	n/a
21	CTCF	chr1:228604020-228604170	GM12866	blood:	n/a	n/a
22	CTCF	chr1:228603920-228604070	HAc	cerebellar:	n/a	n/a
23	CTCF	chr1:228604000-228604150	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr1:228603960-228604110	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr1:228603980-228604130	GM12874	blood:	n/a	n/a
26	CTCF	chr1:228604040-228604190	AG10803	skin:	n/a	n/a
27	CTCF	chr1:228603974-228604166	HepG2	liver:	n/a	n/a
28	CTCF	chr1:228603650-228603660	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr1:228603980-228604130	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr1:228604026-228604028	GM10266	blood:	n/a	n/a
31	CTCF	chr1:228603980-228604130	AG04449	skin:	n/a	n/a
32	CTCF	chr1:228603940-228604090	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr1:228604040-228604190	GM12873	blood:	n/a	n/a
34	CTCF	chr1:228603940-228604090	GM12864	blood:	n/a	n/a
35	CTCF	chr1:228603980-228604130	HAc	cerebellar:	n/a	n/a
36	CTCF	chr1:228604040-228604190	GM12872	blood:	n/a	n/a
37	CTCF	chr1:228604020-228604170	HepG2	liver:	n/a	n/a
38	CTCF	chr1:228604010-228604107	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr1:228603960-228604110	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr1:228603960-228604110	GM06990	blood:	n/a	n/a
41	CTCF	chr1:228603899-228604146	T-47D	breast:	n/a	n/a
42	CTCF	chr1:228604060-228604210	GM12869	blood:	n/a	n/a
43	CTCF	chr1:228603677-228603704	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr1:228604000-228604150	AG09319	gingival:	n/a	n/a
45	CTCF	chr1:228604060-228604210	Caco-2	colon:	n/a	n/a
46	CTCF	chr1:228604154-228604177	GM20000	blood:	n/a	n/a
47	CTCF	chr1:228603980-228604130	HCFaa	heart:	n/a	n/a
48	CTCF	chr1:228604040-228604190	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr1:228603939-228604234	H1-hESC	embryonic stem cell:	n/a	chr1:228604197-228604218
50	CTCF	chr1:228603983-228603996	Pancreas_OC	pancreas:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228604953-228605003	AG04449	skin:	fetal
2	chr1:228603707-228603757	PFSK-1	brain:	n/a
3	chr1:228604240-228604290	AG10803	skin:	n/a
4	chr1:228605477-228605527	ECC-1	luminal epithelium:	n/a
5	chr1:228604037-228604087	NHDF-neo	bronchial:	n/a
6	chr1:228604413-228604463	NT2-D1	testis:	n/a
7	chr1:228604240-228604290	ovcar-3	ovarian:	n/a
8	chr1:228604566-228604616	HRPEpiC	eye:	n/a
9	chr1:228604953-228605003	HepG2	liver:	n/a
10	chr1:228604953-228605003	GM12878	blood:	n/a
11	chr1:228604065-228604115	SK-N-SH_RA	brain:	n/a
12	chr1:228605010-228605060	NB4	blood:	n/a
13	chr1:228604595-228604645	HRPEpiC	eye:	n/a
14	chr1:228603707-228603757	BJ	skin:	n/a
15	chr1:228604037-228604087	AG09319	gingival:	n/a
16	chr1:228603645-228603695	HEK293	kidney:	embryo
17	chr1:228604065-228604115	HRCEpiC	kidney:	n/a
18	chr1:228605477-228605527	HEK293	kidney:	embryo
19	chr1:228605477-228605527	HEEpiC	esophagus:	n/a
20	chr1:228604065-228604115	NHBE	bronchial:	n/a
21	chr1:228604566-228604616	CMK	blood:	n/a
22	chr1:228604953-228605003	GM12892	blood:	n/a
23	chr1:228604595-228604645	HCF	heart:	n/a
24	chr1:228604037-228604087	NH-A	brain:	n/a
25	chr1:228605010-228605060	GM12891	blood:	n/a
26	chr1:228604065-228604115	GM19239	blood:	n/a
27	chr1:228604037-228604087	GM12878	blood:	n/a
28	chr1:228604566-228604616	T-47D	breast:	n/a
29	chr1:228605010-228605060	HCF	heart:	n/a
30	chr1:228605010-228605060	HRCEpiC	kidney:	n/a
31	chr1:228605477-228605527	AG04449	skin:	fetal
32	chr1:228604413-228604463	HCM	heart:	n/a
33	chr1:228604240-228604290	NH-A	brain:	n/a
34	chr1:228604953-228605003	LNCaP	prostate:	n/a
35	chr1:228603707-228603757	HL-60	blood:	n/a
36	chr1:228603645-228603695	HEEpiC	esophagus:	n/a
37	chr1:228604065-228604115	LNCaP	prostate:	n/a
38	chr1:228604037-228604087	GM12891	blood:	n/a
39	chr1:228604595-228604645	Hela-S3	cervix:	n/a
40	chr1:228604240-228604290	ECC-1	luminal epithelium:	n/a
41	chr1:228604953-228605003	K562	blood:	n/a
42	chr1:228604595-228604645	IMR90	lung:	fetal
43	chr1:228603707-228603757	AG04449	skin:	fetal
44	chr1:228605010-228605060	HEEpiC	esophagus:	n/a
45	chr1:228604413-228604463	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:228604800-228604850	HepG2	liver:	n/a
47	chr1:228604566-228604616	HRE	kidney:	n/a
48	chr1:228604037-228604087	HL-60	blood:	n/a
49	chr1:228604240-228604290	NB4	blood:	n/a
50	chr1:228604800-228604850	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:228601250..228603542-chr1:228609261..228610865,3	K562	blood:
2	chr1:228589639..228603795-chr1:228638211..228648676,43	MCF-7	breast:
3	chr1:228585219..228604537-chr1:228641966..228650471,45	MCF-7	breast:

No data

Variant related genes	Relation type
TRIM17	TF binding region
TRIM17	CpG island
ENSG00000196890	chromatin interactions
ENSG00000266174	chromatin interactions
ENSG00000181218	chromatin interactions

Extended variants
information (count: 81 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147693299	chr1:228603387-228603388	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs113565957	chr1:228603392-228603393	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs12124313	chr1:228603434-228603435	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs376664811	chr1:228603446-228603447	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs533161576	chr1:228603452-228603453	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs149149589	chr1:228603454-228603455	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs115416554	chr1:228603466-228603467	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs529431806	chr1:228603475-228603476	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs114435003	chr1:228603480-228603481	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs566266041	chr1:228603511-228603512	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs569427492	chr1:228603530-228603531	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs570111519	chr1:228603553-228603554	Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs532092775	chr1:228603609-228603610	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs550586544	chr1:228603634-228603635	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs535144778	chr1:228603640-228603641	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs548592214	chr1:228603687-228603688	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs568469251	chr1:228603715-228603716	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs537760213	chr1:228603718-228603719	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs557412913	chr1:228603721-228603722	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs192523655	chr1:228603761-228603762	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs143243917	chr1:228603780-228603781	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs370017307	chr1:228603788-228603789	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs577441613	chr1:228603804-228603805	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs535279549	chr1:228603808-228603809	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs555581277	chr1:228603888-228603889	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs575178139	chr1:228603935-228603936	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs544057791	chr1:228603948-228603949	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs151236533	chr1:228604066-228604067	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs184518731	chr1:228604111-228604112	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs540247261	chr1:228604146-228604147	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs560366660	chr1:228604150-228604151	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs529416026	chr1:228604174-228604175	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs542851043	chr1:228604221-228604222	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs397862198	chr1:228604243-228604244	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs538851	chr1:228604248-228604249	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs531950699	chr1:228604298-228604299	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs187444698	chr1:228604342-228604343	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs571994083	chr1:228604367-228604368	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs532924567	chr1:228604408-228604409	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs546610613	chr1:228604462-228604463	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs566425461	chr1:228604473-228604474	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs535575858	chr1:228604594-228604595	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs537478890	chr1:228604609-228604610	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs548812438	chr1:228604675-228604676	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs568661272	chr1:228604742-228604743	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs192832090	chr1:228604743-228604744	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs557596068	chr1:228604777-228604778	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs58462432	chr1:228604788-228604789	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs145864986	chr1:228604791-228604792	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs112240170	chr1:228604846-228604847	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228596000-228603400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr1:228596200-228603400	Weak transcription	NHEK	skin
3	chr1:228596400-228603400	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr1:228596400-228603400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:228596400-228603400	Weak transcription	Pancreas	Pancrea
6	chr1:228596400-228615400	Weak transcription	A549	lung
7	chr1:228596600-228603400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr1:228596600-228603400	Weak transcription	Right Atrium	heart
9	chr1:228597400-228603600	Weak transcription	HMEC	breast
10	chr1:228598600-228603400	Weak transcription	Gastric	stomach
11	chr1:228599000-228603400	Weak transcription	Primary T cells from cord blood	blood
12	chr1:228599400-228603400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:228599400-228603600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:228599800-228603400	Enhancers	Placenta	Placenta
15	chr1:228601000-228603400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:228602200-228603600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:228602400-228603600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr1:228602400-228603600	Enhancers	Spleen	Spleen
19	chr1:228602600-228603600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:228602600-228603600	Enhancers	Ovary	ovary
21	chr1:228602600-228603800	Bivalent Enhancer	Fetal Stomach	stomach
22	chr1:228602800-228603600	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr1:228602800-228603600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
24	chr1:228602800-228603800	Enhancers	Placenta Amnion	Placenta Amnion
25	chr1:228603000-228603400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr1:228603000-228603400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr1:228603000-228603400	Bivalent Enhancer	Fetal Brain Female	brain
28	chr1:228603000-228603400	Enhancers	Fetal Heart	heart
29	chr1:228603000-228603600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
30	chr1:228603000-228603600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
31	chr1:228603000-228603600	Enhancers	Esophagus	oesophagus
32	chr1:228603000-228603600	Bivalent Enhancer	Fetal Intestine Small	intestine
33	chr1:228603000-228603800	Enhancers	Right Ventricle	heart
34	chr1:228603000-228603800	Enhancers	K562	blood
35	chr1:228603000-228604000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:228603000-228605400	Enhancers	Lung	lung
37	chr1:228603200-228603400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr1:228603200-228603400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:228603200-228603400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:228603200-228603400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:228603200-228603400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
42	chr1:228603200-228603400	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr1:228603200-228603400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr1:228603200-228603400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:228603200-228603400	Bivalent Enhancer	Brain Cingulate Gyrus	brain
46	chr1:228603200-228603400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
47	chr1:228603200-228603400	Bivalent Enhancer	Fetal Brain Male	brain
48	chr1:228603200-228603600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:228603200-228603600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr1:228603200-228603600	Active TSS	Brain Anterior Caudate	brain

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