Variant report

Variant	esv3361656
Chromosome Location	chr18:44335579-44338127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:428)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr18:44336050-44336250	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr18:44336734-44336908	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD2	chr18:44336861-44337128	H1-hESC	embryonic stem cell:	n/a	chr18:44337023-44337033
4	CTBP2	chr18:44336144-44337128	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTBP2	chr18:44337460-44338259	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr18:44336840-44336990	GM12871	blood:	n/a	chr18:44336940-44336953
7	CTCF	chr18:44336880-44337030	SK-N-SH_RA	brain:	n/a	chr18:44336940-44336953
8	E2F6	chr18:44336237-44337174	H1-hESC	embryonic stem cell:	n/a	chr18:44336742-44336752 chr18:44337110-44337119 chr18:44336946-44336955
9	E2F6	chr18:44336390-44337100	H1-hESC	embryonic stem cell:	n/a	chr18:44336742-44336752 chr18:44336946-44336955
10	EBF1	chr18:44336453-44336782	GM12878	blood:	n/a	n/a
11	EGR1	chr18:44336812-44337185	H1-hESC	embryonic stem cell:	n/a	chr18:44337025-44337038 chr18:44337024-44337039 chr18:44337079-44337092
12	FOS	chr18:44337421-44337684	HUVEC	blood vessel:	n/a	chr18:44337528-44337538 chr18:44337528-44337538 chr18:44337528-44337538 chr18:44337529-44337537 chr18:44337528-44337538
13	GABPA	chr18:44336146-44337102	H1-hESC	embryonic stem cell:	n/a	chr18:44336584-44336593
14	GABPA	chr18:44336224-44336557	H1-hESC	embryonic stem cell:	n/a	n/a
15	GTF2F1	chr18:44336988-44337000	H1-hESC	embryonic stem cell:	n/a	n/a
16	JUND	chr18:44337854-44338226	H1-hESC	embryonic stem cell:	n/a	n/a
17	JUND	chr18:44336160-44336218	H1-hESC	embryonic stem cell:	n/a	n/a
18	JUND	chr18:44337421-44337654	H1-hESC	embryonic stem cell:	n/a	chr18:44337528-44337538 chr18:44337528-44337538 chr18:44337528-44337538 chr18:44337529-44337537 chr18:44337528-44337538
19	MAX	chr18:44337374-44337780	A549	lung:	n/a	chr18:44337712-44337722
20	MAX	chr18:44336373-44337185	H1-hESC	embryonic stem cell:	n/a	n/a
21	MAX	chr18:44336396-44337176	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAX	chr18:44337432-44337684	A549	lung:	n/a	n/a
23	NANOG	chr18:44336758-44337130	H1-hESC	embryonic stem cell:	n/a	n/a
24	PAX5	chr18:44336494-44336848	GM12892	blood:	n/a	chr18:44336636-44336655
25	POLR2A	chr18:44336809-44336976	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr18:44336843-44337195	H1-neurons	neurons:	n/a	n/a
27	POLR2A	chr18:44336546-44337094	GM18951	blood:	n/a	n/a
28	POLR2A	chr18:44336517-44337122	GM19099	blood:	n/a	n/a
29	POLR2A	chr18:44336760-44337210	H1-neurons	neurons:	n/a	n/a
30	POLR2A	chr18:44337378-44338151	H1-neurons	neurons:	n/a	n/a
31	POLR2A	chr18:44337449-44338015	H1-neurons	neurons:	n/a	n/a
32	RAD21	chr18:44336551-44337128	H1-hESC	embryonic stem cell:	n/a	chr18:44336797-44336811
33	RAD21	chr18:44337631-44337863	H1-hESC	embryonic stem cell:	n/a	n/a
34	SIN3A	chr18:44336701-44337067	H1-hESC	embryonic stem cell:	n/a	chr18:44336701-44336714
35	SIN3A	chr18:44337475-44338191	H1-hESC	embryonic stem cell:	n/a	n/a
36	SIN3AK20	chr18:44336757-44337080	H1-hESC	embryonic stem cell:	n/a	n/a
37	SPI1	chr18:44335295-44335722	HL-60	blood:	n/a	chr18:44335347-44335360 chr18:44335526-44335539
38	TAF1	chr18:44336734-44336930	H1-hESC	embryonic stem cell:	n/a	n/a
39	TBP	chr18:44336671-44337064	H1-hESC	embryonic stem cell:	n/a	n/a
40	TCF3	chr18:44336578-44336991	GM12878	blood:	n/a	n/a
41	USF2	chr18:44336527-44336580	H1-hESC	embryonic stem cell:	n/a	n/a
42	YY1	chr18:44335839-44336473	H1-hESC	embryonic stem cell:	n/a	n/a
43	YY1	chr18:44336764-44337107	H1-hESC	embryonic stem cell:	n/a	chr18:44336810-44336824
44	ZNF384	chr18:44337414-44337471	GM12878	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44337099-44337149	ECC-1	luminal epithelium:	n/a
2	chr18:44337099-44337149	ECC-1	luminal epithelium:	n/a
3	chr18:44338099-44338149	ProgFib	skin:	n/a
4	chr18:44337853-44337903	MCF10A-Er-Src	breast:	n/a
5	chr18:44337910-44337960	H1-hESC	embryonic stem cell:	embryo
6	chr18:44338099-44338149	LNCaP	prostate:	n/a
7	chr18:44336399-44336449	HNPCEpiC	eye:	n/a
8	chr18:44337099-44337149	AG09309	skin:	n/a
9	chr18:44336399-44336449	GM12891	blood:	n/a
10	chr18:44337910-44337960	HPAEpiC	pulmonary alveolar:	n/a
11	chr18:44338099-44338149	MCF-7	breast:	n/a
12	chr18:44336399-44336449	Hela-S3	cervix:	n/a
13	chr18:44336399-44336449	RPTEC	kidney:	n/a
14	chr18:44337664-44337714	NHDF-neo	bronchial:	n/a
15	chr18:44336399-44336449	HPAEpiC	pulmonary alveolar:	n/a
16	chr18:44337099-44337149	A549	lung:	n/a
17	chr18:44337910-44337960	SKMC	muscle:	n/a
18	chr18:44337853-44337903	MCF-7	breast:	n/a
19	chr18:44336399-44336449	SK-N-SH_RA	brain:	n/a
20	chr18:44336399-44336449	HEK293	kidney:	embryo
21	chr18:44337922-44337972	GM12891	blood:	n/a
22	chr18:44337910-44337960	GM12892	blood:	n/a
23	chr18:44337922-44337972	AG04449	skin:	fetal
24	chr18:44337910-44337960	SAEC	small airway:	n/a
25	chr18:44337099-44337149	MCF10A-Er-Src	breast:	n/a
26	chr18:44337853-44337903	HepG2	liver:	n/a
27	chr18:44336399-44336449	SK-N-MC	brain:	n/a
28	chr18:44337853-44337903	HUVEC	blood vessel:	n/a
29	chr18:44337853-44337903	NB4	blood:	n/a
30	chr18:44336399-44336449	H1-hESC	embryonic stem cell:	embryo
31	chr18:44337664-44337714	PFSK-1	brain:	n/a
32	chr18:44337922-44337972	HMEC	breast:	n/a
33	chr18:44336399-44336449	HL-60	blood:	n/a
34	chr18:44337910-44337960	Hela-S3	cervix:	n/a
35	chr18:44338099-44338149	NB4	blood:	n/a
36	chr18:44337099-44337149	NHBE	bronchial:	n/a
37	chr18:44337910-44337960	AG04450	lung:	fetal
38	chr18:44337099-44337149	PrEC	prostate:	n/a
39	chr18:44338099-44338149	PANC-1	pancreas:	n/a
40	chr18:44338099-44338149	HAEpiC	amniotic membrane:	n/a
41	chr18:44337664-44337714	IMR90	lung:	fetal
42	chr18:44337910-44337960	SK-N-SH_RA	brain:	n/a
43	chr18:44336399-44336449	SAEC	small airway:	n/a
44	chr18:44337099-44337149	AG04450	lung:	fetal
45	chr18:44337664-44337714	AG10803	skin:	n/a
46	chr18:44336399-44336449	HUVEC	blood vessel:	n/a
47	chr18:44337922-44337972	HIPEpiC	eye:	n/a
48	chr18:44337922-44337972	GM12892	blood:	n/a
49	chr18:44338099-44338149	RPTEC	kidney:	n/a
50	chr18:44337664-44337714	HL-60	blood:	n/a

No data

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-1	chr18:44337689-44338426	NONHSAT059140
2	lnc-KATNAL2-1	chr18:44336896-44336994	ENSG00000270112.2
3	lnc-KATNAL2-1	chr18:44336746-44337039	ENSG00000270112.2
4	lnc-KATNAL2-1	chr18:44336450-44336587	ENSG00000270112.2

No data

Variant related genes	Relation type
ENSG00000270112	TF binding region
ST8SIA5	TF binding region
ENSG00000270112	CpG island
ST8SIA5	CpG island

Extended variants
information (count: 109 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575251712	chr18:44335589-44335590	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs550534143	chr18:44335619-44335620	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs567312440	chr18:44335647-44335648	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs577733603	chr18:44335659-44335660	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs58095490	chr18:44335667-44335668	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs368854515	chr18:44335669-44335670	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs111731470	chr18:44335690-44335691	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs540741939	chr18:44335723-44335724	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs150279449	chr18:44335724-44335725	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs563208119	chr18:44335856-44335857	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs575084112	chr18:44335868-44335869	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs544216060	chr18:44335884-44335885	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs564133967	chr18:44335891-44335892	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs542147929	chr18:44335903-44335904	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532726055	chr18:44335929-44335930	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs533043982	chr18:44335938-44335939	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs117651431	chr18:44335976-44335977	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs560384291	chr18:44335990-44335991	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs529138660	chr18:44335999-44336000	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs548963836	chr18:44336003-44336004	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs77897901	chr18:44336029-44336030	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs569133962	chr18:44336043-44336044	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs140939580	chr18:44336053-44336054	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs183606963	chr18:44336068-44336069	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs571339105	chr18:44336088-44336089	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs149759000	chr18:44336103-44336104	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs553889624	chr18:44336110-44336111	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs558495058	chr18:44336118-44336119	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs188647618	chr18:44336135-44336136	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs575675107	chr18:44336178-44336179	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs576688870	chr18:44336180-44336181	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs16940042	chr18:44336191-44336192	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs79087688	chr18:44336214-44336215	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs192761864	chr18:44336247-44336248	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs148913302	chr18:44336342-44336343	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs369461751	chr18:44336349-44336350	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs370721700	chr18:44336383-44336384	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs138238211	chr18:44336409-44336410	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs560296820	chr18:44336450-44336451	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs374772249	chr18:44336463-44336464	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs183939959	chr18:44336485-44336486	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs115140167	chr18:44336499-44336500	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs562577812	chr18:44336514-44336515	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs531615122	chr18:44336582-44336583	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs113359876	chr18:44336637-44336638	Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs571298569	chr18:44336640-44336641	Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs527689087	chr18:44336649-44336650	Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs547440641	chr18:44336696-44336697	Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs147005788	chr18:44336700-44336701	Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs35293759	chr18:44336721-44336722	Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44333600-44337400	Bivalent/Poised TSS	Fetal Brain Female	brain
2	chr18:44333800-44335800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
3	chr18:44334000-44335800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr18:44334200-44335600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr18:44334200-44335800	Enhancers	Primary B cells from peripheral blood	blood
6	chr18:44334200-44336200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
7	chr18:44334200-44337800	Active TSS	Brain Angular Gyrus	brain
8	chr18:44334400-44335800	Enhancers	Fetal Heart	heart
9	chr18:44334400-44335800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr18:44334400-44336400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
11	chr18:44334400-44338000	Active TSS	Brain Inferior Temporal Lobe	brain
12	chr18:44334400-44338400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr18:44334600-44335600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
14	chr18:44334600-44335800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr18:44334600-44336000	Active TSS	Brain Germinal Matrix	brain
16	chr18:44334600-44336200	Enhancers	Spleen	Spleen
17	chr18:44334800-44335800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
18	chr18:44334800-44335800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
19	chr18:44334800-44335800	Enhancers	Left Ventricle	heart
20	chr18:44334800-44335800	Weak transcription	Psoas Muscle	Psoas
21	chr18:44334800-44335800	Enhancers	GM12878-XiMat	blood
22	chr18:44335000-44336000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr18:44335000-44336000	Bivalent Enhancer	Fetal Stomach	stomach
24	chr18:44335000-44337600	Active TSS	Right Atrium	heart
25	chr18:44335000-44337800	Active TSS	HSMMtube	muscle
26	chr18:44335200-44335600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr18:44335200-44335600	Flanking Active TSS	Brain Cingulate Gyrus	brain
28	chr18:44335200-44335600	Enhancers	Brain Substantia Nigra	brain
29	chr18:44335200-44335600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
30	chr18:44335200-44335800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
31	chr18:44335200-44336000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr18:44335200-44336000	Active TSS	Brain Hippocampus Middle	brain
33	chr18:44335200-44336200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
34	chr18:44335200-44338200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr18:44335400-44335600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
36	chr18:44335400-44335600	Active TSS	Cortex derived primary cultured neurospheres	brain
37	chr18:44335400-44335600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
38	chr18:44335400-44335800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
39	chr18:44335400-44335800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
40	chr18:44335400-44335800	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
41	chr18:44335400-44335800	Bivalent Enhancer	Fetal Brain Male	brain
42	chr18:44335400-44337400	Bivalent Enhancer	Fetal Lung	lung
43	chr18:44335400-44338200	Active TSS	HSMM	muscle
44	chr18:44335400-44338200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
45	chr18:44335600-44335800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
46	chr18:44335600-44335800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
47	chr18:44335600-44335800	Enhancers	Brain Anterior Caudate	brain
48	chr18:44335600-44335800	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
49	chr18:44335600-44336000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr18:44335600-44336000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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