Variant report

Variant	nsv909356
Chromosome Location	chr18:7493288-7578782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:897)
CpG islands
(count:976)
Chromatin interactive
region (count:18)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:897 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7575137-7575406	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7567159-7567359	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:7567223-7567257	K562	blood:	n/a	n/a
4	ATF2	chr18:7577712-7578133	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr18:7577742-7578206	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr18:7567156-7567368	K562	blood:	n/a	chr18:7567347-7567356 chr18:7567273-7567283
7	BACH1	chr18:7566548-7566660	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr18:7542025-7542029	K562	blood:	n/a	n/a
9	BACH1	chr18:7575526-7576005	H1-hESC	embryonic stem cell:	n/a	chr18:7575877-7575891
10	BACH1	chr18:7566904-7567617	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:7568581-7568843	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr18:7577811-7577975	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr18:7520471-7520649	GM12878	blood:	n/a	chr18:7520557-7520566 chr18:7520557-7520566
14	BHLHE40	chr18:7520520-7520629	K562	blood:	n/a	chr18:7520557-7520566 chr18:7520557-7520566
15	BHLHE40	chr18:7520517-7520690	HepG2	liver:	n/a	chr18:7520557-7520566 chr18:7520557-7520566
16	BHLHE40	chr18:7567045-7567395	GM12878	blood:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
17	BHLHE40	chr18:7566522-7567366	K562	blood:	n/a	chr18:7567340-7567356 chr18:7566691-7566707 chr18:7567117-7567133
18	BHLHE40	chr18:7566784-7567400	HepG2	liver:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
19	BHLHE40	chr18:7575112-7575466	HepG2	liver:	n/a	n/a
20	BRCA1	chr18:7566113-7566632	Hela-S3	cervix:	n/a	n/a
21	CCNT2	chr18:7566537-7567551	K562	blood:	n/a	n/a
22	CEBPB	chr18:7545802-7546128	IMR90	lung:	n/a	n/a
23	CEBPB	chr18:7576856-7577034	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr18:7570005-7570017	A549	lung:	n/a	n/a
25	CEBPB	chr18:7525858-7525917	HepG2	liver:	n/a	chr18:7525887-7525898
26	CEBPB	chr18:7577766-7578084	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr18:7574543-7574739	A549	lung:	n/a	chr18:7574590-7574603
28	CEBPB	chr18:7548380-7548578	HepG2	liver:	n/a	n/a
29	CEBPB	chr18:7577743-7578071	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr18:7545933-7546250	A549	lung:	n/a	n/a
31	CHD1	chr18:7567168-7567252	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr18:7568086-7568380	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr18:7566627-7566933	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr18:7565958-7569508	IMR90	lung:	n/a	chr18:7567084-7567094
35	CHD2	chr18:7566988-7567580	Hela-S3	cervix:	n/a	chr18:7567084-7567094
36	CHD2	chr18:7577748-7578084	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr18:7567294-7567335	HepG2	liver:	n/a	n/a
38	CHD2	chr18:7566721-7566935	K562	blood:	n/a	n/a
39	CHD2	chr18:7566856-7567052	HepG2	liver:	n/a	n/a
40	CHD2	chr18:7568188-7568727	Hela-S3	cervix:	n/a	n/a
41	CREB1	chr18:7566663-7567589	A549	lung:	n/a	n/a
42	CREB1	chr18:7566544-7566952	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr18:7577860-7578056	A549	lung:	n/a	n/a
44	CREB1	chr18:7566858-7567601	HepG2	liver:	n/a	n/a
45	CREB1	chr18:7567120-7567445	A549	lung:	n/a	n/a
46	CREB1	chr18:7567063-7567481	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr18:7567001-7567445	K562	blood:	n/a	n/a
48	CREB1	chr18:7567887-7568154	A549	lung:	n/a	n/a
49	CREB1	chr18:7577691-7578228	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr18:7566645-7567541	H1-hESC	embryonic stem cell:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7568539-7568589	BE2_C	brain:	n/a
2	chr18:7568539-7568589	PrEC	prostate:	n/a
3	chr18:7566656-7566706	NB4	blood:	n/a
4	chr18:7567426-7567476	AG09319	gingival:	n/a
5	chr18:7567548-7567598	NB4	blood:	n/a
6	chr18:7566258-7566308	HCPEpiC	choroid plexus:	n/a
7	chr18:7568891-7568941	HPAEpiC	pulmonary alveolar:	n/a
8	chr18:7567799-7567849	K562	blood:	n/a
9	chr18:7567799-7567849	HMEC	breast:	n/a
10	chr18:7568186-7568236	HIPEpiC	eye:	n/a
11	chr18:7566656-7566706	HPAEpiC	pulmonary alveolar:	n/a
12	chr18:7566656-7566706	PANC-1	pancreas:	n/a
13	chr18:7566558-7566608	BJ	skin:	n/a
14	chr18:7566258-7566308	HRCEpiC	kidney:	n/a
15	chr18:7567638-7567688	HEK293	kidney:	embryo
16	chr18:7566656-7566706	HepG2	liver:	n/a
17	chr18:7568829-7568879	AG09309	skin:	n/a
18	chr18:7566656-7566706	MCF10A-Er-Src	breast:	n/a
19	chr18:7566258-7566308	U87	brain:	n/a
20	chr18:7563847-7563897	NHBE	bronchial:	n/a
21	chr18:7563847-7563897	SKMC	muscle:	n/a
22	chr18:7566258-7566308	BE2_C	brain:	n/a
23	chr18:7567548-7567598	BE2_C	brain:	n/a
24	chr18:7563847-7563897	Hela-S3	cervix:	n/a
25	chr18:7568829-7568879	CMK	blood:	n/a
26	chr18:7567638-7567688	HAEpiC	amniotic membrane:	n/a
27	chr18:7568265-7568315	HIPEpiC	eye:	n/a
28	chr18:7568159-7568209	PrEC	prostate:	n/a
29	chr18:7567717-7567767	ovcar-3	ovarian:	n/a
30	chr18:7567638-7567688	HIPEpiC	eye:	n/a
31	chr18:7567717-7567767	HRCEpiC	kidney:	n/a
32	chr18:7567548-7567598	MCF-7	breast:	n/a
33	chr18:7563847-7563897	GM12892	blood:	n/a
34	chr18:7566258-7566308	AG10803	skin:	n/a
35	chr18:7566558-7566608	HEEpiC	esophagus:	n/a
36	chr18:7567799-7567849	Caco-2	colon:	n/a
37	chr18:7567426-7567476	ECC-1	luminal epithelium:	n/a
38	chr18:7567426-7567476	NB4	blood:	n/a
39	chr18:7568265-7568315	SAEC	small airway:	n/a
40	chr18:7567799-7567849	MCF10A-Er-Src	breast:	n/a
41	chr18:7567638-7567688	A549	lung:	n/a
42	chr18:7568159-7568209	HepG2	liver:	n/a
43	chr18:7563847-7563897	PANC-1	pancreas:	n/a
44	chr18:7567799-7567849	RPTEC	kidney:	n/a
45	chr18:7566656-7566706	PFSK-1	brain:	n/a
46	chr18:7566258-7566308	GM12892	blood:	n/a
47	chr18:7566558-7566608	SAEC	small airway:	n/a
48	chr18:7567717-7567767	AG10803	skin:	n/a
49	chr18:7563847-7563897	GM12878	blood:	n/a
50	chr18:7567638-7567688	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr18:7514458..7516129-chr18:7523489..7525604,2	K562	blood:
2	chr18:7514458..7516129-chr18:7523489..7525604,2	K562	blood:
3	chr18:7560671..7563899-chr18:7566458..7568145,4	K562	blood:
4	chr18:7566319..7569036-chr18:7569097..7573393,5	K562	blood:
5	chr18:7509867..7511990-chr18:7516061..7517678,2	MCF-7	breast:
6	chr18:7504934..7505434-chr3:98276004..98276980,2	HCT-116	colon:
7	chr18:7555198..7557360-chr18:7558467..7560228,2	K562	blood:
8	chr18:7556771..7559463-chr18:7563687..7565562,2	K562	blood:
9	chr18:7561940..7563899-chr18:7566456..7568145,3	K562	blood:
10	chr18:7485561..7489531-chr18:7490547..7493519,3	K562	blood:
11	chr18:7509867..7511990-chr18:7516061..7517678,2	MCF-7	breast:
12	chr18:7556771..7559463-chr18:7563687..7565562,2	K562	blood:
13	chr18:7555198..7557360-chr18:7558467..7560228,2	K562	blood:
14	chr18:7485561..7488328-chr18:7489989..7493519,3	K562	blood:
15	chr18:7560178..7562976-chr18:7564673..7567118,2	MCF-7	breast:
16	chr18:7489323..7491482-chr18:7507564..7509092,2	K562	blood:
17	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:
18	chr18:7567923..7568423-chr20:61846958..61847561,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAMA1-4	chr18:7509140-7509419	XLOC_012749
2	lnc-LAMA1-4	chr18:7508432-7508885	XLOC_012749
3	lnc-LAMA1-4	chr18:7508970-7509053	XLOC_012749

No data

Variant related genes	Relation type
PTPRM	TF binding region
PTPRM	CpG island
ENSG00000173482	chromatin interactions
ENSG00000149658	chromatin interactions

Extended variants
information (count: 2425 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2425 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55946531	chr18:7496057-7496058	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs72636703	chr18:7496058-7496059	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs149859398	chr18:7496123-7496124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184068188	chr18:7496125-7496126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541885091	chr18:7496139-7496140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544923112	chr18:7496151-7496152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145853141	chr18:7496184-7496185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572207756	chr18:7496208-7496209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs516392	chr18:7496209-7496210	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs564272454	chr18:7496225-7496226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533202591	chr18:7496250-7496251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs118081944	chr18:7496268-7496269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563401056	chr18:7496287-7496288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115443496	chr18:7496289-7496290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548666258	chr18:7496290-7496291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565678862	chr18:7496292-7496293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188801733	chr18:7496296-7496297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566019785	chr18:7496307-7496308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78281038	chr18:7496358-7496359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547730207	chr18:7496395-7496396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570699010	chr18:7496417-7496418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs492720	chr18:7496467-7496468	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs16951974	chr18:7496488-7496489	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs140340990	chr18:7496630-7496631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372394521	chr18:7496639-7496640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9951813	chr18:7496664-7496665	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs535957038	chr18:7496717-7496718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549421733	chr18:7496746-7496747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572453325	chr18:7496782-7496783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568962502	chr18:7496836-7496837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537648235	chr18:7496843-7496844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541324133	chr18:7496863-7496864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs59835627	chr18:7496875-7496876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191834178	chr18:7496878-7496879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543615647	chr18:7496903-7496904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143007419	chr18:7496921-7496922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528939865	chr18:7496950-7496951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574029244	chr18:7496953-7496954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs114702431	chr18:7497026-7497027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551303497	chr18:7497073-7497074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147799146	chr18:7497074-7497075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs9966346	chr18:7497079-7497080	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
43	rs111960729	chr18:7497081-7497082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183683142	chr18:7497088-7497089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35636385	chr18:7497098-7497099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533465664	chr18:7497118-7497119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72636704	chr18:7497122-7497123	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545301751	chr18:7497124-7497125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188294200	chr18:7497141-7497142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145077362	chr18:7497144-7497145	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20838587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7496000-7497200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr18:7497400-7497600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr18:7500400-7501000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr18:7500600-7500800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr18:7501000-7502000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr18:7502000-7502600	Enhancers	Placenta	Placenta
7	chr18:7502000-7502800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr18:7502200-7502400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr18:7502200-7502600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr18:7502200-7502600	Enhancers	Fetal Heart	heart
11	chr18:7502200-7502800	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr18:7502200-7502800	Enhancers	HepG2	liver
13	chr18:7502400-7509400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr18:7502600-7503000	Weak transcription	Fetal Heart	heart
15	chr18:7502800-7504400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr18:7503000-7503600	Enhancers	Fetal Heart	heart
17	chr18:7504400-7504800	ZNF genes & repeats	Left Ventricle	heart
18	chr18:7504400-7505000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr18:7504400-7505200	ZNF genes & repeats	Aorta	Aorta
20	chr18:7505200-7514200	Weak transcription	Aorta	Aorta
21	chr18:7508600-7509400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr18:7508800-7510400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr18:7509000-7509200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr18:7509000-7509400	Enhancers	H9 Cell Line	embryonic stem cell
25	chr18:7509000-7509400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr18:7509400-7512000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr18:7509400-7514800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr18:7509800-7510400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr18:7509800-7512000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr18:7510200-7512600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr18:7510400-7514400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr18:7510800-7511800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr18:7511400-7513000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr18:7511600-7512800	Enhancers	Fetal Kidney	kidney
35	chr18:7511800-7512200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr18:7511800-7512200	Enhancers	Pancreas	Pancrea
37	chr18:7511800-7513000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr18:7511800-7513000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr18:7511800-7513400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr18:7511800-7513400	Enhancers	Colon Smooth Muscle	Colon
41	chr18:7512000-7512200	Enhancers	H1 Cell Line	embryonic stem cell
42	chr18:7512000-7513000	Enhancers	Brain Germinal Matrix	brain
43	chr18:7512000-7513200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr18:7512000-7513400	Enhancers	Fetal Brain Male	brain
45	chr18:7512200-7512600	Enhancers	Liver	Liver
46	chr18:7512200-7512600	Enhancers	Brain Anterior Caudate	brain
47	chr18:7512200-7513000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr18:7512200-7513600	Enhancers	Stomach Smooth Muscle	stomach
49	chr18:7512200-7514000	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr18:7512400-7512600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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