Variant report

Variant	nsv576404
Chromosome Location	chr18:7564523-7568644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:575)
CpG islands
(count:794)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7567159-7567359	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7567223-7567257	K562	blood:	n/a	n/a
3	ATF3	chr18:7567156-7567368	K562	blood:	n/a	chr18:7567347-7567356 chr18:7567273-7567283
4	BACH1	chr18:7568581-7568843	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr18:7566548-7566660	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr18:7566904-7567617	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr18:7566784-7567400	HepG2	liver:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
8	BHLHE40	chr18:7566522-7567366	K562	blood:	n/a	chr18:7567340-7567356 chr18:7566691-7566707 chr18:7567117-7567133
9	BHLHE40	chr18:7567045-7567395	GM12878	blood:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
10	BRCA1	chr18:7566113-7566632	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr18:7566537-7567551	K562	blood:	n/a	n/a
12	CHD1	chr18:7567168-7567252	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr18:7565958-7569508	IMR90	lung:	n/a	chr18:7567084-7567094
14	CHD1	chr18:7566627-7566933	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr18:7568086-7568380	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr18:7566988-7567580	Hela-S3	cervix:	n/a	chr18:7567084-7567094
17	CHD2	chr18:7566721-7566935	K562	blood:	n/a	n/a
18	CHD2	chr18:7566856-7567052	HepG2	liver:	n/a	n/a
19	CHD2	chr18:7568188-7568727	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr18:7567294-7567335	HepG2	liver:	n/a	n/a
21	CREB1	chr18:7566645-7567541	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr18:7567063-7567481	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr18:7567001-7567445	K562	blood:	n/a	n/a
24	CREB1	chr18:7567887-7568154	A549	lung:	n/a	n/a
25	CREB1	chr18:7568530-7568853	A549	lung:	n/a	n/a
26	CREB1	chr18:7566858-7567601	HepG2	liver:	n/a	n/a
27	CREB1	chr18:7567120-7567445	A549	lung:	n/a	n/a
28	CREB1	chr18:7566663-7567589	A549	lung:	n/a	n/a
29	CREB1	chr18:7566544-7566952	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr18:7566540-7567821	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr18:7568128-7568834	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr18:7567081-7567353	A549	lung:	n/a	n/a
33	CTCF	chr18:7568522-7568802	LNCaP	prostate:	n/a	n/a
34	CTCF	chr18:7566460-7566610	AG10803	skin:	n/a	n/a
35	CTCF	chr18:7566900-7567050	GM12873	blood:	n/a	n/a
36	CTCF	chr18:7568160-7568310	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr18:7567127-7567412	LNCaP	prostate:	n/a	n/a
38	CTCF	chr18:7567138-7567368	GM10248	blood:	n/a	n/a
39	CTCF	chr18:7566900-7567050	GM12870	blood:	n/a	n/a
40	CTCF	chr18:7567860-7568010	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr18:7567220-7567370	NHLF	lung:	n/a	n/a
42	CTCF	chr18:7567144-7567369	GM19239	blood:	n/a	n/a
43	CTCF	chr18:7567220-7567370	GM12872	blood:	n/a	n/a
44	CTCF	chr18:7568540-7568690	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr18:7566920-7567070	GM12868	blood:	n/a	n/a
46	CTCF	chr18:7567132-7567385	GM12891	blood:	n/a	n/a
47	CTCF	chr18:7567107-7567395	Gliobla	brain:	n/a	n/a
48	CTCF	chr18:7568200-7568350	HAc	cerebellar:	n/a	n/a
49	CTCF	chr18:7567200-7567350	SAEC	small airway:	n/a	n/a
50	CTCF	chr18:7567023-7567417	HepG2	liver:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7568539-7568589	HRPEpiC	eye:	n/a
2	chr18:7568539-7568589	HRPEpiC	eye:	n/a
3	chr18:7567548-7567598	HPAEpiC	pulmonary alveolar:	n/a
4	chr18:7567638-7567688	AG09319	gingival:	n/a
5	chr18:7567548-7567598	AG09319	gingival:	n/a
6	chr18:7567717-7567767	SAEC	small airway:	n/a
7	chr18:7567717-7567767	CMK	blood:	n/a
8	chr18:7568186-7568236	HCF	heart:	n/a
9	chr18:7566558-7566608	NHDF-neo	bronchial:	n/a
10	chr18:7566656-7566706	GM12891	blood:	n/a
11	chr18:7568186-7568236	AG09319	gingival:	n/a
12	chr18:7567717-7567767	HIPEpiC	eye:	n/a
13	chr18:7567717-7567767	Hepatocyte	liver:	n/a
14	chr18:7568159-7568209	K562	blood:	n/a
15	chr18:7566656-7566706	NHBE	bronchial:	n/a
16	chr18:7567799-7567849	NHBE	bronchial:	n/a
17	chr18:7566781-7566831	AG10803	skin:	n/a
18	chr18:7567717-7567767	HepG2	liver:	n/a
19	chr18:7566656-7566706	PANC-1	pancreas:	n/a
20	chr18:7568159-7568209	Hepatocyte	liver:	n/a
21	chr18:7568186-7568236	NB4	blood:	n/a
22	chr18:7566558-7566608	HUVEC	blood vessel:	n/a
23	chr18:7567548-7567598	HepG2	liver:	n/a
24	chr18:7567717-7567767	HPAEpiC	pulmonary alveolar:	n/a
25	chr18:7566656-7566706	SK-N-MC	brain:	n/a
26	chr18:7566781-7566831	NHDF-neo	bronchial:	n/a
27	chr18:7567548-7567598	AG04450	lung:	fetal
28	chr18:7568159-7568209	SK-N-MC	brain:	n/a
29	chr18:7568159-7568209	A549	lung:	n/a
30	chr18:7566558-7566608	AG09319	gingival:	n/a
31	chr18:7567426-7567476	HepG2	liver:	n/a
32	chr18:7567717-7567767	AG04449	skin:	fetal
33	chr18:7568159-7568209	GM12892	blood:	n/a
34	chr18:7567548-7567598	HRE	kidney:	n/a
35	chr18:7567717-7567767	Caco-2	colon:	n/a
36	chr18:7566656-7566706	NHDF-neo	bronchial:	n/a
37	chr18:7568186-7568236	ovcar-3	ovarian:	n/a
38	chr18:7567548-7567598	HCF	heart:	n/a
39	chr18:7567426-7567476	ovcar-3	ovarian:	n/a
40	chr18:7567548-7567598	SK-N-MC	brain:	n/a
41	chr18:7566558-7566608	SK-N-MC	brain:	n/a
42	chr18:7567717-7567767	IMR90	lung:	fetal
43	chr18:7568265-7568315	HPAEpiC	pulmonary alveolar:	n/a
44	chr18:7567426-7567476	H1-hESC	embryonic stem cell:	embryo
45	chr18:7568186-7568236	CMK	blood:	n/a
46	chr18:7567717-7567767	PANC-1	pancreas:	n/a
47	chr18:7566656-7566706	HNPCEpiC	eye:	n/a
48	chr18:7566558-7566608	ECC-1	luminal epithelium:	n/a
49	chr18:7566656-7566706	GM12878	blood:	n/a
50	chr18:7567799-7567849	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr18:7556771..7559463-chr18:7563687..7565562,2	K562	blood:
2	chr18:7567923..7568423-chr20:61846958..61847561,2	MCF-7	breast:
3	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:

No data

Variant related genes	Relation type
PTPRM	TF binding region
PTPRM	CpG island
ENSG00000149658	chromatin interactions

Extended variants
information (count: 128 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:128 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs521887	chr18:7564523-7564524	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201078765	chr18:7564524-7564525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553472071	chr18:7564618-7564619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573151220	chr18:7564629-7564630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565784	chr18:7564653-7564654	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs34465046	chr18:7564695-7564696	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs575573352	chr18:7564771-7564772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544536499	chr18:7564782-7564783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141908361	chr18:7564795-7564796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574587135	chr18:7564828-7564829	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146084106	chr18:7564858-7564859	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560242342	chr18:7564903-7564904	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115630080	chr18:7564919-7564920	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551790713	chr18:7564965-7564966	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183162076	chr18:7564969-7564970	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140139178	chr18:7565032-7565033	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78046641	chr18:7565042-7565043	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565073476	chr18:7565110-7565111	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs369641876	chr18:7565125-7565126	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs567749069	chr18:7565128-7565129	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536897008	chr18:7565142-7565143	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs546755065	chr18:7565144-7565145	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs187843980	chr18:7565161-7565162	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs143760237	chr18:7565221-7565222	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs575366950	chr18:7565222-7565223	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs539149725	chr18:7565230-7565231	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs114899233	chr18:7565232-7565233	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs544091110	chr18:7565233-7565234	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs538100376	chr18:7565266-7565267	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs192422116	chr18:7565285-7565286	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs554891814	chr18:7565309-7565310	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs574545489	chr18:7565340-7565341	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs540450966	chr18:7565357-7565358	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs567230962	chr18:7565392-7565393	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs553572005	chr18:7565423-7565424	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs576495913	chr18:7565424-7565425	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs34787984	chr18:7565425-7565426	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs545515151	chr18:7565478-7565479	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs6506518	chr18:7565514-7565515	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373074304	chr18:7565518-7565519	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs544499947	chr18:7565520-7565521	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs534730725	chr18:7565580-7565581	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs552764004	chr18:7565647-7565648	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs77404597	chr18:7565653-7565654	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs530215353	chr18:7565827-7565828	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs117379744	chr18:7565835-7565836	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs118187234	chr18:7565836-7565837	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs532600911	chr18:7565840-7565841	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs139435332	chr18:7565841-7565842	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs569395983	chr18:7565934-7565935	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Breast cancer	17133270	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	20838587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7558200-7566000	Weak transcription	Right Atrium	heart
2	chr18:7560200-7564600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr18:7560200-7565200	Weak transcription	Psoas Muscle	Psoas
4	chr18:7560200-7566200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr18:7560400-7565200	Weak transcription	Left Ventricle	heart
6	chr18:7560400-7566000	Weak transcription	Lung	lung
7	chr18:7560400-7566000	Weak transcription	Pancreas	Pancrea
8	chr18:7561600-7565600	Enhancers	Colon Smooth Muscle	Colon
9	chr18:7562200-7564800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr18:7562200-7564800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr18:7562200-7564800	Weak transcription	Spleen	Spleen
12	chr18:7562200-7565000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr18:7562200-7565600	Weak transcription	Brain Angular Gyrus	brain
14	chr18:7562200-7565800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr18:7562200-7566000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr18:7562400-7564600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr18:7562400-7564800	Weak transcription	Brain Hippocampus Middle	brain
18	chr18:7562400-7565200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr18:7562400-7565600	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr18:7562400-7565800	Weak transcription	Brain Substantia Nigra	brain
21	chr18:7562400-7566000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr18:7562600-7565600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr18:7562800-7564600	Weak transcription	Adipose Nuclei	Adipose
24	chr18:7562800-7565600	Weak transcription	Brain Anterior Caudate	brain
25	chr18:7562800-7565600	Weak transcription	Fetal Heart	heart
26	chr18:7563200-7564800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr18:7564600-7564800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr18:7564600-7566000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr18:7564600-7566000	Enhancers	Adipose Nuclei	Adipose
30	chr18:7564600-7566400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr18:7564800-7565000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
32	chr18:7564800-7565000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr18:7564800-7565000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr18:7564800-7565000	Bivalent Enhancer	Fetal Thymus	thymus
35	chr18:7564800-7565800	Enhancers	Rectal Smooth Muscle	rectum
36	chr18:7564800-7566000	Enhancers	Brain Cingulate Gyrus	brain
37	chr18:7564800-7566000	Enhancers	Brain Hippocampus Middle	brain
38	chr18:7565000-7565200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr18:7565000-7565200	Enhancers	Spleen	Spleen
40	chr18:7565000-7565800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr18:7565000-7565800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr18:7565000-7566000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr18:7565000-7566000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr18:7565000-7566000	Enhancers	Right Ventricle	heart
45	chr18:7565000-7566000	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr18:7565200-7565400	Enhancers	Left Ventricle	heart
47	chr18:7565200-7565600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
48	chr18:7565200-7565600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
49	chr18:7565200-7565800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr18:7565200-7565800	Enhancers	NHDF-Ad	bronchial

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