Variant report

Variant	nsv432488
Chromosome Location	chr3:140752302-140790302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:492)
CpG islands
(count:2138)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:140769669-140770314	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr3:140789636-140790184	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:140789628-140790245	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:140770618-140770876	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:140769922-140770142	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:140789806-140790174	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr3:140771576-140771976	H1-hESC	embryonic stem cell:	n/a	chr3:140771835-140771844
8	BRCA1	chr3:140784680-140784744	HepG2	liver:	n/a	n/a
9	CEBPB	chr3:140789045-140789433	H1-hESC	embryonic stem cell:	n/a	chr3:140789230-140789241
10	CEBPB	chr3:140755974-140756121	IMR90	lung:	n/a	n/a
11	CEBPB	chr3:140765953-140766496	HCT-116	colon:	n/a	n/a
12	CEBPB	chr3:140779285-140779372	K562	blood:	n/a	n/a
13	CEBPB	chr3:140769888-140770174	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr3:140766043-140766379	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:140789054-140789377	HepG2	liver:	n/a	chr3:140789230-140789241
16	CEBPB	chr3:140789062-140789421	K562	blood:	n/a	chr3:140789230-140789241
17	CEBPB	chr3:140765949-140766549	HCT-116	colon:	n/a	n/a
18	CEBPB	chr3:140789690-140790502	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr3:140789114-140789389	A549	lung:	n/a	chr3:140789230-140789241
20	CEBPB	chr3:140789079-140789346	Hela-S3	cervix:	n/a	chr3:140789230-140789241
21	CEBPB	chr3:140789067-140789353	MCF-7	breast:	n/a	chr3:140789230-140789241
22	CEBPB	chr3:140789067-140789388	IMR90	lung:	n/a	chr3:140789230-140789241
23	CHD1	chr3:140770451-140770569	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr3:140769682-140770094	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr3:140771582-140772030	H1-hESC	embryonic stem cell:	n/a	chr3:140771835-140771844 chr3:140771761-140771771
26	CHD2	chr3:140769691-140770376	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr3:140770599-140771129	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr3:140789718-140790253	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr3:140789698-140790249	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr3:140769410-140770971	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr3:140789600-140790353	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr3:140769940-140770090	GM12872	blood:	n/a	chr3:140770040-140770053 chr3:140770041-140770051 chr3:140770040-140770053 chr3:140770038-140770056
33	CTCF	chr3:140768723-140768812	NHEK	skin:	n/a	n/a
34	CTCF	chr3:140768723-140768861	GM12878	blood:	n/a	n/a
35	CTCF	chr3:140768700-140768850	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr3:140768840-140768990	GM12874	blood:	n/a	n/a
37	CTCF	chr3:140769900-140770050	HMEC	breast:	n/a	n/a
38	CTCF	chr3:140770520-140770670	AG09319	gingival:	n/a	n/a
39	CTCF	chr3:140769895-140770147	H1-hESC	embryonic stem cell:	n/a	chr3:140770040-140770053 chr3:140770041-140770051 chr3:140770040-140770053 chr3:140770038-140770056
40	CTCF	chr3:140768590-140768959	K562	blood:	n/a	n/a
41	CTCF	chr3:140770573-140770797	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr3:140768640-140768790	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr3:140768680-140768830	SAEC	small airway:	n/a	n/a
44	CTCF	chr3:140768570-140769059	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:140769940-140770090	BE2_C	brain:	n/a	chr3:140770040-140770053 chr3:140770041-140770051 chr3:140770040-140770053 chr3:140770038-140770056
46	CTCF	chr3:140769940-140770090	HBMEC	blood vessel:	n/a	chr3:140770040-140770053 chr3:140770041-140770051 chr3:140770040-140770053 chr3:140770038-140770056
47	CTCF	chr3:140770546-140770754	A549	lung:	n/a	n/a
48	CTCF	chr3:140769724-140771185	SK-N-SH	brain:	n/a	chr3:140770040-140770053 chr3:140770041-140770051 chr3:140770040-140770053 chr3:140770038-140770056
49	CTCF	chr3:140768736-140768818	LNCaP	prostate:	n/a	n/a
50	CTCF	chr3:140769920-140770070	HCT-116	colon:	n/a	chr3:140770040-140770053 chr3:140770041-140770051 chr3:140770040-140770053 chr3:140770038-140770056

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140770345-140770395	AG10803	skin:	n/a
2	chr3:140771372-140771422	HCM	heart:	n/a
3	chr3:140769814-140769864	GM19239	blood:	n/a
4	chr3:140770345-140770395	AG10803	skin:	n/a
5	chr3:140771372-140771422	HCM	heart:	n/a
6	chr3:140769814-140769864	GM19239	blood:	n/a
7	chr3:140770617-140770667	SKMC	muscle:	n/a
8	chr3:140784989-140785039	Hepatocyte	liver:	n/a
9	chr3:140770588-140770638	HCF	heart:	n/a
10	chr3:140770306-140770356	MCF-7	breast:	n/a
11	chr3:140770308-140770358	HNPCEpiC	eye:	n/a
12	chr3:140788453-140788503	HCF	heart:	n/a
13	chr3:140785160-140785210	SK-N-MC	brain:	n/a
14	chr3:140770345-140770395	HRE	kidney:	n/a
15	chr3:140785473-140785523	Caco-2	colon:	n/a
16	chr3:140771184-140771234	HRCEpiC	kidney:	n/a
17	chr3:140770617-140770667	MCF-7	breast:	n/a
18	chr3:140785473-140785523	MCF-7	breast:	n/a
19	chr3:140770013-140770063	HL-60	blood:	n/a
20	chr3:140770683-140770733	H1-hESC	embryonic stem cell:	embryo
21	chr3:140784675-140784725	Hepatocyte	liver:	n/a
22	chr3:140770599-140770649	AG04449	skin:	fetal
23	chr3:140770213-140770263	ovcar-3	ovarian:	n/a
24	chr3:140785160-140785210	HAEpiC	amniotic membrane:	n/a
25	chr3:140771372-140771422	MCF-7	breast:	n/a
26	chr3:140785160-140785210	NT2-D1	testis:	n/a
27	chr3:140771656-140771706	Hepatocyte	liver:	n/a
28	chr3:140769691-140769741	MCF10A-Er-Src	breast:	n/a
29	chr3:140785160-140785210	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:140770013-140770063	ProgFib	skin:	n/a
31	chr3:140783430-140783480	ECC-1	luminal epithelium:	n/a
32	chr3:140770683-140770733	HCF	heart:	n/a
33	chr3:140784989-140785039	ovcar-3	ovarian:	n/a
34	chr3:140770864-140770914	BJ	skin:	n/a
35	chr3:140770683-140770733	HCT-116	colon:	n/a
36	chr3:140770013-140770063	RPTEC	kidney:	n/a
37	chr3:140770864-140770914	HRE	kidney:	n/a
38	chr3:140770588-140770638	MCF-7	breast:	n/a
39	chr3:140769814-140769864	NHBE	bronchial:	n/a
40	chr3:140788453-140788503	HUVEC	blood vessel:	n/a
41	chr3:140788453-140788503	HCPEpiC	choroid plexus:	n/a
42	chr3:140769274-140769324	NT2-D1	testis:	n/a
43	chr3:140787055-140787105	Jurkat	blood:	n/a
44	chr3:140771184-140771234	GM12891	blood:	n/a
45	chr3:140788453-140788503	ProgFib	skin:	n/a
46	chr3:140784185-140784235	Hela-S3	cervix:	n/a
47	chr3:140770345-140770395	GM19239	blood:	n/a
48	chr3:140770608-140770658	HPAEpiC	pulmonary alveolar:	n/a
49	chr3:140770213-140770263	ProgFib	skin:	n/a
50	chr3:140787055-140787105	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:140774491..140777455-chr3:140795854..140797381,2	K562	blood:
2	chr3:140769622..140773131-chr3:140773940..140776930,3	MCF-7	breast:
3	chr3:140782511..140785350-chr3:140792921..140794807,2	K562	blood:
4	chr3:140762813..140764824-chr3:140768643..140770363,2	MCF-7	breast:
5	chr3:140789496..140791213-chr3:140794078..140795843,2	K562	blood:
6	chr3:140763223..140765937-chr3:140775586..140778392,2	K562	blood:
7	chr3:140730075..140730963-chr3:140768335..140768843,2	MCF-7	breast:
8	chr17:33477684..33478239-chr3:140770419..140770939,2	MCF-7	breast:
9	chr3:140766170..140768825-chr3:140770762..140772841,2	MCF-7	breast:
10	chr3:140737164..140739325-chr3:140761875..140763616,2	MCF-7	breast:
11	chr3:140785419..140788357-chr3:140788951..140791966,3	MCF-7	breast:
12	chr3:140779965..140781663-chr3:140785163..140787679,2	K562	blood:
13	chr3:140768713..140769273-chr3:140910536..140911423,2	MCF-7	breast:
14	chr3:140785941..140788584-chr3:140792512..140794344,2	MCF-7	breast:
15	chr3:140763223..140765937-chr3:140775586..140778392,2	K562	blood:
16	chr3:140660042..140662305-chr3:140787345..140789644,2	K562	blood:
17	chr3:140766170..140768825-chr3:140770762..140772841,2	MCF-7	breast:
18	chr3:140789863..140792661-chr3:140847892..140850124,2	MCF-7	breast:

No data

Variant related genes	Relation type
SPSB4	TF binding region
SPSB4	CpG island
ENSG00000175093	chromatin interactions
ENSG00000114120	chromatin interactions

Extended variants
information (count: 1273 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1273 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75269307	chr3:140754804-140754805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537822547	chr3:140754859-140754860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs151141594	chr3:140754873-140754874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373478716	chr3:140754917-140754918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs5026385	chr3:140754940-140754941	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535793032	chr3:140754975-140754976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73868965	chr3:140755030-140755031	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs534177717	chr3:140755072-140755073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572585278	chr3:140755091-140755092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540299632	chr3:140755094-140755095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs59691029	chr3:140755108-140755109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376166175	chr3:140755275-140755276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs193014350	chr3:140755287-140755288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562473498	chr3:140755295-140755296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185151433	chr3:140755296-140755297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573861633	chr3:140755312-140755313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533670091	chr3:140755358-140755359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560376217	chr3:140755362-140755363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189216878	chr3:140755383-140755384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192429635	chr3:140755386-140755387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552113372	chr3:140755395-140755396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140041907	chr3:140755397-140755398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183724526	chr3:140755404-140755405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549761349	chr3:140755405-140755406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568154914	chr3:140755514-140755515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9816809	chr3:140755578-140755579	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs537067447	chr3:140755601-140755602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572718970	chr3:140755612-140755613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539607962	chr3:140755628-140755629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558337834	chr3:140755669-140755670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576819359	chr3:140755722-140755723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544371523	chr3:140755750-140755751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562459916	chr3:140755763-140755764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574521810	chr3:140755789-140755790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542124028	chr3:140755792-140755793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567660789	chr3:140755808-140755809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560161177	chr3:140755821-140755822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527599330	chr3:140755831-140755832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552046480	chr3:140755860-140755861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564352804	chr3:140755945-140755946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116404413	chr3:140755979-140755980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549894934	chr3:140755987-140755988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9876562	chr3:140755988-140755989	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs529219537	chr3:140756016-140756017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547399604	chr3:140756027-140756028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566200554	chr3:140756028-140756029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35243333	chr3:140756043-140756044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368505459	chr3:140756073-140756074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35345445	chr3:140756083-140756084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540126539	chr3:140756092-140756093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Schizophrenia	17989066	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:746 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140754800-140755400	Enhancers	Brain Germinal Matrix	brain
2	chr3:140755400-140758400	Weak transcription	Brain Germinal Matrix	brain
3	chr3:140758400-140758800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr3:140758400-140758800	Enhancers	Brain Germinal Matrix	brain
5	chr3:140758600-140759200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr3:140758600-140759200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr3:140758600-140759200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr3:140759200-140764000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr3:140759200-140764000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr3:140763800-140764200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:140764000-140765200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr3:140764000-140765400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr3:140764000-140766000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr3:140764200-140764600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr3:140764400-140764800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr3:140764400-140764800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr3:140764400-140765000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr3:140764400-140765200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr3:140764600-140765200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr3:140764800-140765000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr3:140764800-140765200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr3:140764800-140769400	Weak transcription	Right Atrium	heart
23	chr3:140765200-140765400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr3:140765400-140767000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr3:140765800-140766600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr3:140765800-140766600	Enhancers	NHEK	skin
27	chr3:140765800-140766800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:140766000-140766600	Enhancers	HMEC	breast
29	chr3:140766200-140766800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:140766400-140766600	Bivalent Enhancer	Placenta	Placenta
31	chr3:140766400-140767000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr3:140766600-140766800	Bivalent Enhancer	HMEC	breast
33	chr3:140766600-140767000	Bivalent Enhancer	NHEK	skin
34	chr3:140767000-140767200	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr3:140767000-140769400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr3:140768800-140769000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
37	chr3:140769000-140769400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr3:140769000-140769400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
39	chr3:140769000-140769400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr3:140769000-140769400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:140769000-140769800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr3:140769000-140769800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
43	chr3:140769000-140770000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr3:140769000-140770000	Flanking Active TSS	Dnd41	blood
45	chr3:140769200-140769400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
46	chr3:140769200-140769400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
47	chr3:140769200-140769400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
48	chr3:140769200-140769400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
49	chr3:140769200-140769400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
50	chr3:140769200-140769400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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