Variant report

Variant	nsv437346
Chromosome Location	chr1:223903781-223905532
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:223887434..223890501-chr1:223901110..223904266,3	K562	blood:
2	chr1:223891592..223893967-chr1:223903233..223904840,2	K562	blood:
3	chr1:223900439..223903816-chr1:223918326..223920507,3	MCF-7	breast:
4	chr1:223884407..223886063-chr1:223901694..223904527,2	K562	blood:
5	chr1:223903418..223905687-chr1:223928822..223931791,2	MCF-7	breast:
6	chr1:223902286..223903884-chr1:223996819..223998348,2	K562	blood:
7	chr1:223903451..223905300-chr1:223920938..223923297,2	MCF-7	breast:
8	chr1:223901725..223903941-chr1:223941728..223943865,2	MCF-7	breast:
9	chr1:223904247..223905976-chr1:223916920..223919197,2	MCF-7	breast:
10	chr1:223901394..223904242-chr1:223919607..223921227,2	K562	blood:
11	chr1:223885961..223896993-chr1:223898177..223910405,32	MCF-7	breast:
12	chr1:223895202..223897591-chr1:223904463..223906328,2	K562	blood:
13	chr1:223904423..223906015-chr1:223946207..223948782,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000162909	chromatin interactions

Extended variants
information (count: 77 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:77 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10495215	chr1:223903781-223903782	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142567789	chr1:223903817-223903818	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs28370017	chr1:223903826-223903827	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs574433784	chr1:223903828-223903829	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535687321	chr1:223903862-223903863	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs150546506	chr1:223903868-223903869	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576036139	chr1:223903891-223903892	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs16842040	chr1:223903926-223903927	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs75870440	chr1:223903940-223903941	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559036640	chr1:223903989-223903990	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs558225579	chr1:223904002-223904003	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs372582697	chr1:223904135-223904136	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182498810	chr1:223904198-223904199	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540577944	chr1:223904225-223904226	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562054052	chr1:223904233-223904234	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529358103	chr1:223904241-223904242	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139460747	chr1:223904242-223904243	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs563125546	chr1:223904259-223904260	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs28370018	chr1:223904277-223904278	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs75702065	chr1:223904313-223904314	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs17557288	chr1:223904323-223904324	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs534819445	chr1:223904334-223904335	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373575246	chr1:223904338-223904339	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs570677830	chr1:223904346-223904347	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs528083396	chr1:223904381-223904382	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554717895	chr1:223904382-223904383	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568085349	chr1:223904401-223904402	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535513616	chr1:223904406-223904407	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557624005	chr1:223904438-223904439	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569466091	chr1:223904461-223904462	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372604099	chr1:223904469-223904470	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs187000979	chr1:223904475-223904476	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147845688	chr1:223904508-223904509	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs60587982	chr1:223904577-223904578	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs28370019	chr1:223904578-223904579	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs10495216	chr1:223904595-223904596	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs28370020	chr1:223904606-223904607	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs563227374	chr1:223904694-223904695	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191533000	chr1:223904695-223904696	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs546779334	chr1:223904713-223904714	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145204191	chr1:223904724-223904725	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184229893	chr1:223904728-223904729	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576769530	chr1:223904760-223904761	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs147616603	chr1:223904810-223904811	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530621005	chr1:223904846-223904847	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs571428442	chr1:223904856-223904857	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149154722	chr1:223904857-223904858	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528359697	chr1:223904872-223904873	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546307506	chr1:223904876-223904877	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs540749887	chr1:223904920-223904921	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223900800-223904400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
2	chr1:223900800-223906000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr1:223901000-223903800	Flanking Active TSS	HUVEC	blood vessel
4	chr1:223901000-223904200	Flanking Active TSS	Stomach Smooth Muscle	stomach
5	chr1:223901000-223905200	Enhancers	Spleen	Spleen
6	chr1:223901000-223905800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr1:223901200-223904600	Enhancers	Small Intestine	intestine
8	chr1:223901200-223904800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:223901200-223905400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:223901400-223904400	Transcr. at gene 5' and 3'	NHLF	lung
11	chr1:223901400-223904800	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
12	chr1:223901400-223905600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:223901400-223907600	Transcr. at gene 5' and 3'	A549	lung
14	chr1:223901600-223903800	Enhancers	Primary T cells from cord blood	blood
15	chr1:223901600-223903800	Enhancers	Fetal Intestine Small	intestine
16	chr1:223901600-223904000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr1:223901600-223904200	Enhancers	Brain Angular Gyrus	brain
18	chr1:223901600-223904200	Enhancers	Placenta	Placenta
19	chr1:223901600-223904600	Enhancers	Brain Hippocampus Middle	brain
20	chr1:223901600-223905200	Transcr. at gene 5' and 3'	NHEK	skin
21	chr1:223901600-223905800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:223901600-223906200	Enhancers	Primary B cells from peripheral blood	blood
23	chr1:223901600-223906400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr1:223901800-223903800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr1:223901800-223904000	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:223901800-223904000	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr1:223901800-223904000	Weak transcription	Aorta	Aorta
28	chr1:223901800-223904000	Enhancers	Brain Cingulate Gyrus	brain
29	chr1:223901800-223904000	Enhancers	Fetal Intestine Large	intestine
30	chr1:223901800-223904000	Transcr. at gene 5' and 3'	Osteobl	bone
31	chr1:223901800-223904200	Enhancers	Lung	lung
32	chr1:223901800-223904400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr1:223901800-223904600	Enhancers	Right Atrium	heart
34	chr1:223901800-223904800	Enhancers	Fetal Brain Female	brain
35	chr1:223901800-223905000	Enhancers	Fetal Heart	heart
36	chr1:223901800-223905000	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr1:223901800-223905200	Enhancers	Placenta Amnion	Placenta Amnion
38	chr1:223901800-223905600	Genic enhancers	Fetal Muscle Trunk	muscle
39	chr1:223901800-223905800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr1:223901800-223906200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr1:223902000-223903800	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:223902000-223903800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr1:223902000-223904400	Enhancers	Brain Anterior Caudate	brain
44	chr1:223902000-223905000	Enhancers	Fetal Brain Male	brain
45	chr1:223902200-223904400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr1:223902200-223904600	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr1:223902200-223904800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr1:223902200-223904800	Genic enhancers	Fetal Stomach	stomach
49	chr1:223902200-223905200	Genic enhancers	Fetal Muscle Leg	muscle
50	chr1:223902200-223913400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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