Variant report

Variant	nsv516128
Chromosome Location	chr18:11683431-11695676
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr18:11688949-11689352	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr18:11688929-11689329	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr18:11694384-11694509	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr18:11688898-11689396	A549	lung:	n/a	chr18:11689212-11689225
5	BCLAF1	chr18:11688882-11689263	GM12878	blood:	n/a	chr18:11689212-11689225
6	BHLHE40	chr18:11689049-11689223	GM12878	blood:	n/a	chr18:11689063-11689079 chr18:11689071-11689087
7	BRCA1	chr18:11688994-11689271	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr18:11689014-11689222	HepG2	liver:	n/a	n/a
9	CBX3	chr18:11688887-11689477	HCT-116	colon:	n/a	n/a
10	CBX3	chr18:11689017-11689205	K562	blood:	n/a	n/a
11	CEBPB	chr18:11688849-11689294	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr18:11688981-11689299	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr18:11689001-11689165	HepG2	liver:	n/a	n/a
14	CHD2	chr18:11688938-11689375	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr18:11688956-11689350	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr18:11689732-11689887	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr18:11689034-11689298	HepG2	liver:	n/a	n/a
18	CHD2	chr18:11688992-11689266	GM12878	blood:	n/a	n/a
19	CHD2	chr18:11689709-11689973	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr18:11689038-11689242	K562	blood:	n/a	n/a
21	CREB1	chr18:11689027-11689339	A549	lung:	n/a	n/a
22	CREB1	chr18:11688947-11689343	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr18:11688913-11689398	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr18:11688927-11690111	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr18:11695112-11695162	Fibrobl	skin:	n/a	n/a
26	CTCF	chr18:11689040-11689274	K562	blood:	n/a	n/a
27	CTCF	chr18:11689063-11689203	NHEK	skin:	n/a	n/a
28	CTCF	chr18:11689020-11689170	Caco-2	colon:	n/a	chr18:11689031-11689044
29	CTCF	chr18:11689160-11689310	GM12874	blood:	n/a	n/a
30	CTCF	chr18:11688920-11689070	NHEK	skin:	n/a	chr18:11689031-11689044
31	CTCF	chr18:11689135-11689143	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr18:11689104-11689172	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr18:11689115-11689174	Fibrobl	skin:	n/a	n/a
34	CTCF	chr18:11689020-11689170	HCPEpiC	choroid plexus:	n/a	chr18:11689031-11689044
35	CUX1	chr18:11688494-11688584	GM12878	blood:	n/a	n/a
36	E2F1	chr18:11689177-11689687	Hela-S3	cervix:	n/a	chr18:11689451-11689463 chr18:11689217-11689227 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11689451-11689462 chr18:11689487-11689498 chr18:11689538-11689548
37	E2F4	chr18:11688499-11688765	MCF10A-Er-Src	breast:	n/a	chr18:11688546-11688553 chr18:11688546-11688553 chr18:11688546-11688553
38	E2F4	chr18:11688969-11689595	MCF10A-Er-Src	breast:	n/a	chr18:11689451-11689463 chr18:11689217-11689227 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11689538-11689548
39	E2F6	chr18:11688898-11690144	H1-hESC	embryonic stem cell:	n/a	chr18:11690080-11690089 chr18:11689451-11689463 chr18:11689217-11689227 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11690084-11690093 chr18:11689538-11689548
40	E2F6	chr18:11689491-11690092	A549	lung:	n/a	chr18:11690080-11690089 chr18:11689546-11689561 chr18:11689534-11689543 chr18:11689538-11689548
41	E2F6	chr18:11689026-11690136	H1-hESC	embryonic stem cell:	n/a	chr18:11690080-11690089 chr18:11689451-11689463 chr18:11689217-11689227 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11690084-11690093 chr18:11689538-11689548
42	E2F6	chr18:11689667-11689856	K562	blood:	n/a	n/a
43	E2F6	chr18:11689431-11689596	K562	blood:	n/a	chr18:11689451-11689463 chr18:11689546-11689561 chr18:11689487-11689499 chr18:11689534-11689543 chr18:11689538-11689548
44	E2F6	chr18:11689607-11690010	K562	blood:	n/a	n/a
45	E2F6	chr18:11689552-11690113	A549	lung:	n/a	chr18:11690080-11690089 chr18:11690084-11690093
46	EBF1	chr18:11690214-11690358	GM12878	blood:	n/a	chr18:11690271-11690280
47	EGR1	chr18:11688938-11689277	H1-hESC	embryonic stem cell:	n/a	chr18:11689240-11689250
48	EGR1	chr18:11689416-11689666	K562	blood:	n/a	chr18:11689552-11689562 chr18:11689538-11689551 chr18:11689538-11689551 chr18:11689538-11689548 chr18:11689539-11689549 chr18:11689539-11689548 chr18:11689538-11689551
49	EGR1	chr18:11688973-11689292	H1-hESC	embryonic stem cell:	n/a	chr18:11689240-11689250
50	ELF1	chr18:11689024-11689270	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:11685789-11685839	HAEpiC	amniotic membrane:	n/a
2	chr18:11685789-11685839	HAEpiC	amniotic membrane:	n/a
3	chr18:11688008-11688058	SKMC	muscle:	n/a
4	chr18:11685789-11685839	H1-hESC	embryonic stem cell:	embryo
5	chr18:11689218-11689268	HCT-116	colon:	n/a
6	chr18:11689284-11689334	HAEpiC	amniotic membrane:	n/a
7	chr18:11688011-11688061	LNCaP	prostate:	n/a
8	chr18:11688772-11688822	HNPCEpiC	eye:	n/a
9	chr18:11689613-11689663	H1-hESC	embryonic stem cell:	embryo
10	chr18:11688772-11688822	HRCEpiC	kidney:	n/a
11	chr18:11688972-11689022	CMK	blood:	n/a
12	chr18:11685789-11685839	K562	blood:	n/a
13	chr18:11689062-11689112	K562	blood:	n/a
14	chr18:11688972-11689022	NHDF-neo	bronchial:	n/a
15	chr18:11688772-11688822	GM12892	blood:	n/a
16	chr18:11689032-11689082	HCM	heart:	n/a
17	chr18:11689218-11689268	HCPEpiC	choroid plexus:	n/a
18	chr18:11689613-11689663	HRCEpiC	kidney:	n/a
19	chr18:11688988-11689038	Jurkat	blood:	n/a
20	chr18:11689284-11689334	ProgFib	skin:	n/a
21	chr18:11689032-11689082	SKMC	muscle:	n/a
22	chr18:11692420-11692470	GM19239	blood:	n/a
23	chr18:11688011-11688061	MCF-7	breast:	n/a
24	chr18:11690145-11690195	ECC-1	luminal epithelium:	n/a
25	chr18:11689032-11689082	AoSMC	blood vessel:	n/a
26	chr18:11688011-11688061	NH-A	brain:	n/a
27	chr18:11685789-11685839	IMR90	lung:	fetal
28	chr18:11689024-11689074	GM12878	blood:	n/a
29	chr18:11689206-11689256	MCF-7	breast:	n/a
30	chr18:11689613-11689663	HEK293	kidney:	embryo
31	chr18:11692420-11692470	Hepatocyte	liver:	n/a
32	chr18:11689062-11689112	HEK293	kidney:	embryo
33	chr18:11692420-11692470	NH-A	brain:	n/a
34	chr18:11688988-11689038	HCF	heart:	n/a
35	chr18:11689613-11689663	K562	blood:	n/a
36	chr18:11689206-11689256	IMR90	lung:	fetal
37	chr18:11689613-11689663	ovcar-3	ovarian:	n/a
38	chr18:11690145-11690195	HL-60	blood:	n/a
39	chr18:11689613-11689663	NHDF-neo	bronchial:	n/a
40	chr18:11688008-11688058	HRE	kidney:	n/a
41	chr18:11688988-11689038	IMR90	lung:	fetal
42	chr18:11692420-11692470	AoSMC	blood vessel:	n/a
43	chr18:11689218-11689268	SK-N-SH	brain:	n/a
44	chr18:11689284-11689334	HNPCEpiC	eye:	n/a
45	chr18:11689206-11689256	NHDF-neo	bronchial:	n/a
46	chr18:11689024-11689074	Caco-2	colon:	n/a
47	chr18:11689284-11689334	SKMC	muscle:	n/a
48	chr18:11690145-11690195	AG04449	skin:	fetal
49	chr18:11689024-11689074	CMK	blood:	n/a
50	chr18:11689613-11689663	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:11661437..11663649-chr18:11686391..11688864,2	K562	blood:
2	chr18:11662625..11665139-chr18:11684651..11687441,2	MCF-7	breast:
3	chr18:11665029..11667238-chr18:11692110..11694200,2	K562	blood:

Variant related genes	Relation type
GNAL	TF binding region
GNAL	CpG island

Extended variants
information (count: 434 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8097337	chr18:11683431-11683432	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552325824	chr18:11683454-11683455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538774655	chr18:11683480-11683481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs80094328	chr18:11683495-11683496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534934711	chr18:11683524-11683525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141924463	chr18:11683633-11683634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566085215	chr18:11683651-11683652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150671590	chr18:11683677-11683678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117921456	chr18:11683696-11683697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576597802	chr18:11683726-11683727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs137924073	chr18:11683735-11683736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536442444	chr18:11683790-11683791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559120870	chr18:11683810-11683811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372274314	chr18:11683837-11683838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560573038	chr18:11683874-11683875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370757335	chr18:11683887-11683888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142490076	chr18:11683898-11683899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs8097296	chr18:11683955-11683956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376512100	chr18:11684000-11684001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116032433	chr18:11684007-11684008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35925878	chr18:11684017-11684018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs534538369	chr18:11684153-11684154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371027168	chr18:11684157-11684158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541406468	chr18:11684179-11684180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs80266346	chr18:11684180-11684181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530539953	chr18:11684225-11684226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551954354	chr18:11684277-11684278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145936240	chr18:11684301-11684302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546526328	chr18:11684383-11684384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139835940	chr18:11684387-11684388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546922364	chr18:11684388-11684389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34372518	chr18:11684511-11684512	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536680044	chr18:11684540-11684541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554981450	chr18:11684552-11684553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12606122	chr18:11684559-11684560	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs11080531	chr18:11684605-11684606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs112391610	chr18:11684606-11684607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184966035	chr18:11684641-11684642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77043413	chr18:11684648-11684649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12606108	chr18:11684657-11684658	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553282791	chr18:11684836-11684837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574768695	chr18:11684876-11684877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77233873	chr18:11685003-11685004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75413843	chr18:11685033-11685034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550706164	chr18:11685073-11685074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79195391	chr18:11685096-11685097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564841623	chr18:11685119-11685120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12454527	chr18:11685122-11685123	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs77895094	chr18:11685126-11685127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528329167	chr18:11685211-11685212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
Melanoma	18172304	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
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11677200-11688400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr18:11688200-11688400	Enhancers	Hela-S3	cervix
3	chr18:11688400-11688600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
4	chr18:11688400-11688600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr18:11688400-11688600	Enhancers	Brain Hippocampus Middle	brain
6	chr18:11688400-11688600	Enhancers	Colon Smooth Muscle	Colon
7	chr18:11688400-11688600	Enhancers	Stomach Smooth Muscle	stomach
8	chr18:11688400-11688800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
9	chr18:11688400-11688800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr18:11688400-11688800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr18:11688400-11689000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr18:11688400-11689000	Flanking Active TSS	Hela-S3	cervix
13	chr18:11688400-11689400	Active TSS	Fetal Brain Female	brain
14	chr18:11688600-11688800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
15	chr18:11688600-11688800	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
16	chr18:11688600-11688800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
17	chr18:11688600-11688800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr18:11688600-11688800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr18:11688600-11688800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr18:11688600-11688800	Bivalent Enhancer	Liver	Liver
21	chr18:11688600-11688800	Enhancers	Brain Anterior Caudate	brain
22	chr18:11688600-11688800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
23	chr18:11688600-11688800	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
24	chr18:11688600-11688800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
25	chr18:11688600-11688800	Bivalent Enhancer	Fetal Heart	heart
26	chr18:11688600-11688800	Bivalent Enhancer	Fetal Kidney	kidney
27	chr18:11688600-11688800	Bivalent Enhancer	Fetal Muscle Leg	muscle
28	chr18:11688600-11688800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
29	chr18:11688600-11688800	Enhancers	NHEK	skin
30	chr18:11688600-11689000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr18:11688600-11689000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
32	chr18:11688600-11689000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
33	chr18:11688600-11689000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
34	chr18:11688600-11689000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr18:11688600-11689000	Flanking Active TSS	Brain Hippocampus Middle	brain
36	chr18:11688600-11689000	Bivalent Enhancer	Fetal Lung	lung
37	chr18:11688600-11689000	Bivalent Enhancer	Fetal Stomach	stomach
38	chr18:11688600-11689200	Flanking Active TSS	Colon Smooth Muscle	Colon
39	chr18:11688600-11689200	Bivalent Enhancer	Fetal Thymus	thymus
40	chr18:11688600-11689200	Flanking Active TSS	Stomach Smooth Muscle	stomach
41	chr18:11688600-11690200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
42	chr18:11688600-11690200	Active TSS	Rectal Smooth Muscle	rectum
43	chr18:11688600-11690400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr18:11688600-11690400	Active TSS	A549	lung
45	chr18:11688600-11690600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
46	chr18:11688600-11690600	Active TSS	HMEC	breast
47	chr18:11688800-11689000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
48	chr18:11688800-11689000	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr18:11688800-11689000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr18:11688800-11689000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell

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