Variant report

Variant	nsv582498
Chromosome Location	chr2:97639135-97715154
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:1038)
Chromatin interactive
region (count:12)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:97678106-97678242	K562	blood:	n/a	n/a
2	ARID3A	chr2:97678092-97678206	HepG2	liver:	n/a	n/a
3	BACH1	chr2:97643257-97643537	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:97703210-97703532	GM12878	blood:	n/a	chr2:97703363-97703374
5	BATF	chr2:97703257-97703526	GM12878	blood:	n/a	chr2:97703363-97703374
6	BCL11A	chr2:97700319-97700488	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:97652345-97652458	K562	blood:	n/a	n/a
8	BRCA1	chr2:97659412-97659454	GM12878	blood:	n/a	n/a
9	CEBPB	chr2:97643679-97643973	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:97678094-97678135	K562	blood:	n/a	n/a
11	CEBPB	chr2:97678022-97678244	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:97643711-97643923	A549	lung:	n/a	n/a
13	CTCF	chr2:97678040-97678190	RPTEC	kidney:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
14	CTCF	chr2:97677973-97678266	Spleen_OC	spleen:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
15	CTCF	chr2:97678080-97678230	GM12871	blood:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
16	CTCF	chr2:97671974-97671998	GM10248	blood:	n/a	n/a
17	CTCF	chr2:97671283-97671327	MCF-7	breast:	n/a	n/a
18	CTCF	chr2:97671160-97671310	GM12864	blood:	n/a	n/a
19	CTCF	chr2:97678060-97678210	HL-60	blood:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
20	CTCF	chr2:97670360-97670510	GM12875	blood:	n/a	n/a
21	CTCF	chr2:97678040-97678190	HFF-Myc	foreskin:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
22	CTCF	chr2:97670420-97670570	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr2:97671200-97671350	RPTEC	kidney:	n/a	n/a
24	CTCF	chr2:97677608-97677629	GM10248	blood:	n/a	n/a
25	CTCF	chr2:97678040-97678190	HBMEC	blood vessel:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
26	CTCF	chr2:97678040-97678190	HPF	lung:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
27	CTCF	chr2:97671240-97671390	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr2:97678040-97678190	SAEC	small airway:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
29	CTCF	chr2:97678003-97678212	Gliobla	brain:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
30	CTCF	chr2:97678040-97678190	HAc	cerebellar:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
31	CTCF	chr2:97671220-97671370	HFF	foreskin:	n/a	n/a
32	CTCF	chr2:97678032-97678188	SK-N-SH_RA	brain:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
33	CTCF	chr2:97671160-97671310	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr2:97670400-97670550	GM12873	blood:	n/a	n/a
35	CTCF	chr2:97677985-97678216	H1-hESC	embryonic stem cell:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
36	CTCF	chr2:97671136-97671570	K562	blood:	n/a	n/a
37	CTCF	chr2:97671196-97671385	K562	blood:	n/a	n/a
38	CTCF	chr2:97671277-97671312	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:97671200-97671350	BJ	skin:	n/a	n/a
40	CTCF	chr2:97657935-97658031	LNCaP	prostate:	n/a	n/a
41	CTCF	chr2:97671160-97671310	GM12869	blood:	n/a	n/a
42	CTCF	chr2:97678035-97678218	GM13976	blood:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
43	CTCF	chr2:97671200-97671350	HepG2	liver:	n/a	n/a
44	CTCF	chr2:97671200-97671350	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr2:97678016-97678206	GM13977	blood:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
46	CTCF	chr2:97670360-97670510	Caco-2	colon:	n/a	n/a
47	CTCF	chr2:97671220-97671370	NHLF	lung:	n/a	n/a
48	CTCF	chr2:97672301-97672358	GM20000	blood:	n/a	n/a
49	CTCF	chr2:97678060-97678210	HPAF	blood vessel:	n/a	chr2:97678125-97678146 chr2:97678123-97678141
50	CTCF	chr2:97670360-97670510	GM12864	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:97652440-97652490	T-47D	breast:	n/a
2	chr2:97652440-97652490	T-47D	breast:	n/a
3	chr2:97653250-97653300	K562	blood:	n/a
4	chr2:97653250-97653300	PFSK-1	brain:	n/a
5	chr2:97655388-97655438	HNPCEpiC	eye:	n/a
6	chr2:97652440-97652490	MCF10A-Er-Src	breast:	n/a
7	chr2:97699471-97699521	HCPEpiC	choroid plexus:	n/a
8	chr2:97651765-97651815	SKMC	muscle:	n/a
9	chr2:97652491-97652541	HCM	heart:	n/a
10	chr2:97699471-97699521	HRE	kidney:	n/a
11	chr2:97652129-97652179	AG04450	lung:	fetal
12	chr2:97650711-97650761	AG04449	skin:	fetal
13	chr2:97700249-97700299	CMK	blood:	n/a
14	chr2:97652806-97652856	HRE	kidney:	n/a
15	chr2:97652249-97652299	AG09319	gingival:	n/a
16	chr2:97652806-97652856	K562	blood:	n/a
17	chr2:97651611-97651661	H1-hESC	embryonic stem cell:	embryo
18	chr2:97652249-97652299	AG10803	skin:	n/a
19	chr2:97699471-97699521	NHBE	bronchial:	n/a
20	chr2:97649526-97649576	SK-N-SH	brain:	n/a
21	chr2:97652129-97652179	SKMC	muscle:	n/a
22	chr2:97653560-97653610	AG04450	lung:	fetal
23	chr2:97653560-97653610	NB4	blood:	n/a
24	chr2:97653250-97653300	HCF	heart:	n/a
25	chr2:97700249-97700299	SAEC	small airway:	n/a
26	chr2:97655388-97655438	HRPEpiC	eye:	n/a
27	chr2:97653250-97653300	HIPEpiC	eye:	n/a
28	chr2:97652491-97652541	SK-N-SH	brain:	n/a
29	chr2:97651765-97651815	GM12891	blood:	n/a
30	chr2:97679964-97680014	HL-60	blood:	n/a
31	chr2:97652129-97652179	AoSMC	blood vessel:	n/a
32	chr2:97700249-97700299	SK-N-SH_RA	brain:	n/a
33	chr2:97650711-97650761	PANC-1	pancreas:	n/a
34	chr2:97653560-97653610	HCPEpiC	choroid plexus:	n/a
35	chr2:97700249-97700299	SKMC	muscle:	n/a
36	chr2:97652806-97652856	MCF-7	breast:	n/a
37	chr2:97649526-97649576	HMEC	breast:	n/a
38	chr2:97655388-97655438	LNCaP	prostate:	n/a
39	chr2:97650711-97650761	BJ	skin:	n/a
40	chr2:97651765-97651815	IMR90	lung:	fetal
41	chr2:97655388-97655438	AG10803	skin:	n/a
42	chr2:97700249-97700299	GM12892	blood:	n/a
43	chr2:97653560-97653610	HEEpiC	esophagus:	n/a
44	chr2:97651765-97651815	HNPCEpiC	eye:	n/a
45	chr2:97652491-97652541	Hepatocyte	liver:	n/a
46	chr2:97650711-97650761	HNPCEpiC	eye:	n/a
47	chr2:97652491-97652541	ECC-1	luminal epithelium:	n/a
48	chr2:97649526-97649576	AG04450	lung:	fetal
49	chr2:97650711-97650761	HCF	heart:	n/a
50	chr2:97652806-97652856	CMK	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:97522290..97524000-chr2:97650084..97651689,2	K562	blood:
2	chr2:97481579..97482495-chr2:97650048..97650628,3	MCF-7	breast:
3	chr2:97503295..97505354-chr2:97640763..97643321,2	MCF-7	breast:
4	chr2:97480657..97482301-chr2:97648745..97651504,3	MCF-7	breast:
5	chr2:97482890..97484803-chr2:97649558..97651545,2	MCF-7	breast:
6	chr2:97636377..97638575-chr2:97641382..97642951,2	K562	blood:
7	chr2:97481713..97482226-chr2:97650010..97650560,2	MCF-7	breast:
8	chr2:97632347..97633971-chr2:97643638..97646130,2	MCF-7	breast:
9	chr2:97480449..97482310-chr2:97649600..97651617,3	MCF-7	breast:
10	chr2:97481553..97482385-chr2:97650007..97650622,6	MCF-7	breast:
11	chr2:97677657..97678211-chr2:97777841..97778623,2	K562	blood:
12	chr2:97481522..97482261-chr2:97650059..97650610,3	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD36-8	chr2:97712325-97712628	NONHSAT072601
2	lnc-ANKRD36-9	chr2:97700179-97700443	NONHSAT072600
3	lnc-FAM178B-2	chr2:97696245-97696347	NONHSAT072599
4	lnc-FAM178B-2	chr2:97697265-97697373	NONHSAT072599
5	lnc-FAM178B-2	chr2:97693296-97693401	NONHSAT072599
6	lnc-FAM178B-2	chr2:97694949-97695180	NONHSAT072599
7	lnc-FAM178B-3	chr2:97706960-97707312	predAs_ge08_ZAP70_1
8	lnc-FAM178B-1	chr2:97684080-97684341	NONHSAT072598
9	lnc-FAM178B-2	chr2:97691718-97692195	NONHSAT072599

No data

Variant related genes	Relation type
FAM178B	TF binding region
ENSG00000248134	TF binding region
TRIM43CP	TF binding region
IGKV2OR2-2	TF binding region
ENSG00000230343	TF binding region
IGKV2OR2-1	TF binding region
ENSG00000238760	TF binding region
ENSG00000236847	TF binding region
FAM178B	CpG island
ENSG00000248134	CpG island
TRIM43CP	CpG island
IGKV2OR2-2	CpG island
ENSG00000230343	CpG island
IGKV2OR2-1	CpG island
ENSG00000238760	CpG island
ENSG00000236847	CpG island
ENSG00000168763	chromatin interactions
ENSG00000163126	chromatin interactions
ENSG00000213337	chromatin interactions

Extended variants
information (count: 1316 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1257017	chr2:97639135-97639136	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551558767	chr2:97639149-97639150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571727591	chr2:97639156-97639157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149388440	chr2:97639273-97639274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181844927	chr2:97639312-97639313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577794815	chr2:97639496-97639497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567546030	chr2:97639507-97639508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540096251	chr2:97639548-97639549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536598030	chr2:97639610-97639611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558698811	chr2:97639660-97639661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573160261	chr2:97639725-97639726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144732053	chr2:97639726-97639727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558856823	chr2:97639825-97639826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185400360	chr2:97639845-97639846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558478176	chr2:97639846-97639847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563335123	chr2:97639853-97639854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528891722	chr2:97639872-97639873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542598070	chr2:97639894-97639895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559692558	chr2:97639916-97639917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528358119	chr2:97639960-97639961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570199837	chr2:97639991-97639992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551572474	chr2:97640032-97640033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189966360	chr2:97640042-97640043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531076649	chr2:97640107-97640108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77424574	chr2:97640118-97640119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537628866	chr2:97640178-97640179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75514725	chr2:97640217-97640218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181266745	chr2:97640271-97640272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536258844	chr2:97640300-97640301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552914846	chr2:97640450-97640451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1257016	chr2:97640502-97640503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs367948830	chr2:97640530-97640531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144411092	chr2:97640553-97640554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184890444	chr2:97640556-97640557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575739409	chr2:97640607-97640608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111688742	chr2:97640625-97640626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190807904	chr2:97640634-97640635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556783839	chr2:97640635-97640636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184008773	chr2:97640664-97640665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12616466	chr2:97640671-97640672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs545618362	chr2:97640706-97640707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113322658	chr2:97640710-97640711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187399543	chr2:97640721-97640722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559361107	chr2:97640730-97640731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140195628	chr2:97640743-97640744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544966823	chr2:97640753-97640754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191741407	chr2:97640760-97640761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530623357	chr2:97640804-97640805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550712924	chr2:97640829-97640830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112107572	chr2:97640833-97640834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:97620800-97643600	Weak transcription	Right Atrium	heart
2	chr2:97633200-97643200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr2:97634600-97642200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:97636400-97643200	Weak transcription	Fetal Kidney	kidney
5	chr2:97636600-97643200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr2:97636600-97643400	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr2:97636800-97643000	Weak transcription	A549	lung
8	chr2:97637400-97643200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr2:97638200-97639200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr2:97638400-97647600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:97639200-97643200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr2:97641000-97643400	Weak transcription	Fetal Lung	lung
13	chr2:97641800-97643400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr2:97642200-97644200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:97642600-97643200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:97643000-97643200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr2:97643000-97643200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr2:97643000-97643200	Weak transcription	Brain Anterior Caudate	brain
19	chr2:97643000-97643200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr2:97643000-97643200	Enhancers	A549	lung
21	chr2:97643000-97643400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr2:97643000-97644000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr2:97643000-97644000	Enhancers	HMEC	breast
24	chr2:97643200-97643400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr2:97643200-97643400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr2:97643200-97643400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr2:97643200-97643400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr2:97643200-97643400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:97643200-97643400	Flanking Active TSS	Brain Anterior Caudate	brain
30	chr2:97643200-97643400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr2:97643200-97643400	Active TSS	Brain Substantia Nigra	brain
32	chr2:97643200-97643400	Enhancers	HSMM	muscle
33	chr2:97643200-97643400	Enhancers	K562	blood
34	chr2:97643200-97643400	Enhancers	NHDF-Ad	bronchial
35	chr2:97643200-97643600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr2:97643200-97643600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:97643200-97643600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr2:97643200-97643600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:97643200-97643600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr2:97643200-97643600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr2:97643200-97643600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr2:97643200-97643600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
43	chr2:97643200-97643600	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr2:97643200-97643600	Flanking Active TSS	Fetal Kidney	kidney
45	chr2:97643200-97643600	Enhancers	Rectal Smooth Muscle	rectum
46	chr2:97643200-97643600	Flanking Active TSS	A549	lung
47	chr2:97643200-97643600	Flanking Active TSS	HSMMtube	muscle
48	chr2:97643200-97643800	Active TSS	Brain Cingulate Gyrus	brain
49	chr2:97643200-97643800	Active TSS	Brain Hippocampus Middle	brain
50	chr2:97643200-97644000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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