Variant report

Variant	esv34706
Chromosome Location	chr2:205309211-205348724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:358)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:205334895-205335181	K562	blood:	n/a	n/a
2	ARID3A	chr2:205317329-205317588	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:205348269-205348449	K562	blood:	n/a	n/a
4	ATF1	chr2:205334924-205335186	K562	blood:	n/a	n/a
5	ATF1	chr2:205337198-205337490	K562	blood:	n/a	n/a
6	ATF3	chr2:205334933-205335237	K562	blood:	n/a	n/a
7	BATF	chr2:205344293-205344619	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:205316258-205316421	K562	blood:	n/a	n/a
9	BHLHE40	chr2:205348625-205348749	K562	blood:	n/a	n/a
10	BHLHE40	chr2:205337135-205337399	K562	blood:	n/a	n/a
11	BHLHE40	chr2:205319224-205319229	K562	blood:	n/a	n/a
12	BHLHE40	chr2:205348196-205348389	K562	blood:	n/a	n/a
13	BRCA1	chr2:205338012-205338332	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr2:205317187-205317387	K562	blood:	n/a	n/a
15	CCNT2	chr2:205334937-205335179	K562	blood:	n/a	n/a
16	CCNT2	chr2:205348218-205348734	K562	blood:	n/a	n/a
17	CEBPB	chr2:205333404-205333700	K562	blood:	n/a	chr2:205333577-205333588
18	CEBPB	chr2:205337148-205337456	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:205334865-205335319	K562	blood:	n/a	n/a
20	CEBPB	chr2:205347390-205347603	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:205333493-205333738	A549	lung:	n/a	chr2:205333577-205333588
22	CEBPB	chr2:205319524-205319674	HepG2	liver:	n/a	chr2:205319592-205319603
23	CEBPB	chr2:205337975-205338360	Hela-S3	cervix:	n/a	chr2:205338172-205338184
24	CEBPB	chr2:205334946-205335218	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:205334825-205335382	HCT-116	colon:	n/a	n/a
26	CEBPB	chr2:205344277-205344524	A549	lung:	n/a	n/a
27	CEBPB	chr2:205333405-205333765	K562	blood:	n/a	chr2:205333577-205333588
28	CEBPB	chr2:205333401-205334289	Hela-S3	cervix:	n/a	chr2:205333577-205333588
29	CEBPB	chr2:205334795-205335276	HCT-116	colon:	n/a	n/a
30	CEBPB	chr2:205319550-205319606	K562	blood:	n/a	chr2:205319592-205319603
31	CEBPB	chr2:205334815-205335330	K562	blood:	n/a	n/a
32	CEBPB	chr2:205317031-205317962	IMR90	lung:	n/a	chr2:205317146-205317159 chr2:205317303-205317314
33	CEBPB	chr2:205333405-205333747	HepG2	liver:	n/a	chr2:205333577-205333588
34	CEBPB	chr2:205334895-205335255	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:205344250-205344631	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:205333505-205333705	H1-hESC	embryonic stem cell:	n/a	chr2:205333577-205333588
37	CEBPB	chr2:205342382-205342697	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:205334907-205335215	K562	blood:	n/a	n/a
39	CEBPB	chr2:205333390-205334403	IMR90	lung:	n/a	chr2:205333577-205333588
40	CEBPB	chr2:205334862-205335282	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr2:205317385-205317435	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr2:205337331-205337350	K562	blood:	n/a	n/a
43	CTCF	chr2:205318720-205318870	HBMEC	blood vessel:	n/a	chr2:205318811-205318818
44	CTCF	chr2:205334944-205334958	GM10248	blood:	n/a	n/a
45	CTCF	chr2:205327676-205327775	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr2:205317300-205317450	AG10803	skin:	n/a	n/a
47	CTCF	chr2:205317460-205317610	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr2:205317340-205317490	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr2:205337216-205337502	K562	blood:	n/a	n/a
50	CTCF	chr2:205317300-205317450	HCPEpiC	choroid plexus:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:205333978-205334028	Hela-S3	cervix:	n/a
2	chr2:205333978-205334028	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:205333978-205334028	H1-hESC	embryonic stem cell:	embryo
4	chr2:205333978-205334028	ECC-1	luminal epithelium:	n/a
5	chr2:205333978-205334028	GM19239	blood:	n/a
6	chr2:205333978-205334028	HMEC	breast:	n/a
7	chr2:205333978-205334028	HRE	kidney:	n/a
8	chr2:205333978-205334028	HIPEpiC	eye:	n/a
9	chr2:205333978-205334028	MCF10A-Er-Src	breast:	n/a
10	chr2:205333978-205334028	HUVEC	blood vessel:	n/a
11	chr2:205333978-205334028	U87	brain:	n/a
12	chr2:205333978-205334028	AG09319	gingival:	n/a
13	chr2:205333978-205334028	BE2_C	brain:	n/a
14	chr2:205333978-205334028	ProgFib	skin:	n/a
15	chr2:205333978-205334028	HRCEpiC	kidney:	n/a
16	chr2:205333978-205334028	AG10803	skin:	n/a
17	chr2:205333978-205334028	HCT-116	colon:	n/a
18	chr2:205333978-205334028	SK-N-MC	brain:	n/a
19	chr2:205333978-205334028	GM06990	blood:	n/a
20	chr2:205333978-205334028	NT2-D1	testis:	n/a
21	chr2:205333978-205334028	BJ	skin:	n/a
22	chr2:205333978-205334028	HEK293	kidney:	embryo
23	chr2:205333978-205334028	HL-60	blood:	n/a
24	chr2:205333978-205334028	NH-A	brain:	n/a
25	chr2:205333978-205334028	CMK	blood:	n/a
26	chr2:205333978-205334028	MCF-7	breast:	n/a
27	chr2:205333978-205334028	SAEC	small airway:	n/a
28	chr2:205333978-205334028	HNPCEpiC	eye:	n/a
29	chr2:205333978-205334028	AG04450	lung:	fetal
30	chr2:205333978-205334028	NB4	blood:	n/a
31	chr2:205333978-205334028	SKMC	muscle:	n/a
32	chr2:205333978-205334028	K562	blood:	n/a
33	chr2:205333978-205334028	Jurkat	blood:	n/a
34	chr2:205333978-205334028	SK-N-SH	brain:	n/a
35	chr2:205333978-205334028	GM12892	blood:	n/a
36	chr2:205333978-205334028	NHDF-neo	bronchial:	n/a
37	chr2:205333978-205334028	PrEC	prostate:	n/a
38	chr2:205333978-205334028	HCM	heart:	n/a
39	chr2:205333978-205334028	PFSK-1	brain:	n/a
40	chr2:205333978-205334028	HCF	heart:	n/a
41	chr2:205333978-205334028	ovcar-3	ovarian:	n/a
42	chr2:205333978-205334028	Hepatocyte	liver:	n/a
43	chr2:205333978-205334028	Caco-2	colon:	n/a
44	chr2:205333978-205334028	GM12878	blood:	n/a
45	chr2:205333978-205334028	SK-N-SH_RA	brain:	n/a
46	chr2:205333978-205334028	IMR90	lung:	fetal
47	chr2:205333978-205334028	GM12891	blood:	n/a
48	chr2:205333978-205334028	AG04449	skin:	fetal
49	chr2:205333978-205334028	A549	lung:	n/a
50	chr2:205333978-205334028	PANC-1	pancreas:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:205314742..205317390-chr2:205323844..205326602,2	K562	blood:
2	chr2:205342371..205345502-chr2:205347551..205349331,3	MCF-7	breast:
3	chr2:205347876..205350145-chr2:205365321..205368902,4	K562	blood:
4	chr2:205314792..205317401-chr2:205318306..205319999,2	K562	blood:
5	chr2:205314792..205317401-chr2:205318306..205319999,2	K562	blood:
6	chr2:205317459..205320428-chr2:205333008..205336253,3	K562	blood:
7	chr2:205216295..205217937-chr2:205321013..205323112,2	K562	blood:
8	chr2:205318766..205320712-chr2:205322486..205325283,3	K562	blood:
9	chr2:205317294..205319471-chr2:205340816..205343787,2	K562	blood:
10	chr2:205317299..205320276-chr2:205333008..205336367,3	K562	blood:
11	chr2:205318766..205320712-chr2:205322486..205325283,3	K562	blood:
12	chr2:205269954..205272543-chr2:205315221..205317326,2	K562	blood:
13	chr2:205317299..205320276-chr2:205333008..205336367,3	K562	blood:
14	chr2:205345447..205347577-chr2:205349288..205350850,2	K562	blood:
15	chr2:205314742..205317390-chr2:205323844..205326602,2	K562	blood:
16	chr2:205342371..205345502-chr2:205347551..205349331,3	MCF-7	breast:
17	chr2:205317459..205320428-chr2:205333008..205336253,3	K562	blood:
18	chr2:205341764..205344115-chr2:205410157..205412057,2	MCF-7	breast:
19	chr2:205317294..205319471-chr2:205340816..205343787,2	K562	blood:
20	chr2:205334439..205337199-chr2:205337976..205341222,3	K562	blood:
21	chr2:205347876..205349851-chr2:205365321..205368563,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAPH1-3	chr2:205334799-205335174	XLOC_002470
2	lnc-RAPH1-3	chr2:205338349-205338560	XLOC_002470
3	lnc-PARD3B-1	chr2:205340079-205340346	XLOC_001815

No data

Variant related genes	Relation type
ENSG00000236634	TF binding region
ENSG00000237843	TF binding region
ENSG00000236634	CpG island
ENSG00000237843	CpG island
ENSG00000237843	chromatin interactions
ENSG00000116117	chromatin interactions
ENSG00000236634	chromatin interactions
CELSR3	miRNA target sites

Extended variants
information (count: 1145 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11690070	chr2:205309211-205309212	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574710102	chr2:205309214-205309215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527857487	chr2:205309258-205309259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552851440	chr2:205309280-205309281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76608425	chr2:205309286-205309287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138739303	chr2:205309336-205309337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs58713677	chr2:205309368-205309369	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs199628824	chr2:205309369-205309370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568456234	chr2:205309381-205309382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182424799	chr2:205309489-205309490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554287317	chr2:205309603-205309604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187101147	chr2:205309628-205309629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2121682	chr2:205309670-205309671	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs532384089	chr2:205309700-205309701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192868553	chr2:205309728-205309729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142790529	chr2:205309743-205309744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185442403	chr2:205309801-205309802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147405816	chr2:205309853-205309854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188758833	chr2:205309886-205309887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139729876	chr2:205309925-205309926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540752578	chr2:205309957-205309958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78436487	chr2:205309965-205309966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527897666	chr2:205310025-205310026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142672602	chr2:205310026-205310027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369412023	chr2:205310033-205310034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564702414	chr2:205310035-205310036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532088232	chr2:205310048-205310049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566880079	chr2:205310049-205310050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371588867	chr2:205310117-205310118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529277579	chr2:205310266-205310267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs202034506	chr2:205310272-205310273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76017501	chr2:205310292-205310293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1447494	chr2:205310411-205310412	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs565999203	chr2:205310432-205310433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193205911	chr2:205310453-205310454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551331084	chr2:205310463-205310464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114519417	chr2:205310472-205310473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77069015	chr2:205310493-205310494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150595854	chr2:205310512-205310513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573321755	chr2:205310534-205310535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139251158	chr2:205310559-205310560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375625140	chr2:205310591-205310592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553036855	chr2:205310595-205310596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577711939	chr2:205310627-205310628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184949530	chr2:205310663-205310664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564562734	chr2:205310664-205310665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188150015	chr2:205310669-205310670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4522588	chr2:205310670-205310671	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535834915	chr2:205310688-205310689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531463219	chr2:205310735-205310736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Cervical cancer	21062161	CNVD
Intracranial aneurysm	16715129	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205304000-205314200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr2:205312800-205314600	Enhancers	Rectal Smooth Muscle	rectum
3	chr2:205313600-205316600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:205313600-205316800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:205313800-205316000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:205313800-205317000	Enhancers	Colon Smooth Muscle	Colon
7	chr2:205314000-205314200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:205314000-205320000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr2:205314200-205316600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:205314200-205316800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:205314400-205314600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr2:205314400-205315600	Enhancers	Brain Hippocampus Middle	brain
13	chr2:205314600-205315400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:205314600-205315400	Weak transcription	Rectal Smooth Muscle	rectum
15	chr2:205314600-205319800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr2:205314800-205315600	Enhancers	Brain Anterior Caudate	brain
17	chr2:205314800-205315600	Enhancers	Brain Substantia Nigra	brain
18	chr2:205314800-205315800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:205315000-205315200	Enhancers	Fetal Brain Male	brain
20	chr2:205315000-205315600	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr2:205315200-205316000	Enhancers	K562	blood
22	chr2:205315400-205315600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:205315400-205315600	Enhancers	Rectal Smooth Muscle	rectum
24	chr2:205315400-205315800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr2:205315400-205316400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr2:205315400-205316600	Weak transcription	Fetal Brain Male	brain
27	chr2:205315600-205315800	Enhancers	Fetal Lung	lung
28	chr2:205315600-205316000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr2:205315600-205317400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:205315600-205318400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr2:205315600-205318400	Weak transcription	Brain Substantia Nigra	brain
32	chr2:205315600-205318800	Weak transcription	Brain Anterior Caudate	brain
33	chr2:205315800-205316200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:205315800-205316200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:205315800-205316400	Weak transcription	Fetal Lung	lung
36	chr2:205316000-205316400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:205316000-205316400	Weak transcription	K562	blood
38	chr2:205316000-205318400	Enhancers	Rectal Smooth Muscle	rectum
39	chr2:205316200-205316400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr2:205316200-205316400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:205316200-205316400	Enhancers	Lung	lung
42	chr2:205316200-205317600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr2:205316400-205316600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:205316400-205316600	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr2:205316400-205316800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:205316400-205316800	Enhancers	K562	blood
47	chr2:205316400-205316800	Enhancers	NHLF	lung
48	chr2:205316400-205317000	Enhancers	Fetal Lung	lung
49	chr2:205316400-205317000	Enhancers	HUVEC	blood vessel
50	chr2:205316400-205317200	Enhancers	A549	lung

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