Variant report

Variant	nsv997638
Chromosome Location	chr2:172442205-172560406
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1379)
CpG islands
(count:1039)
Chromatin interactive
region (count:70)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1379 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:172455255-172455609	K562	blood:	n/a	n/a
2	ARID3A	chr2:172545111-172545114	K562	blood:	n/a	n/a
3	ARID3A	chr2:172487937-172488103	K562	blood:	n/a	n/a
4	ARID3A	chr2:172455256-172455598	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:172560121-172560443	K562	blood:	n/a	n/a
6	ARID3A	chr2:172543762-172544429	HepG2	liver:	n/a	n/a
7	ATF1	chr2:172543731-172544411	K562	blood:	n/a	n/a
8	ATF1	chr2:172487618-172488114	K562	blood:	n/a	n/a
9	ATF1	chr2:172524870-172525035	K562	blood:	n/a	n/a
10	ATF1	chr2:172539136-172539281	K562	blood:	n/a	n/a
11	ATF2	chr2:172543680-172544432	GM12878	blood:	n/a	n/a
12	ATF2	chr2:172487847-172488188	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr2:172543597-172544140	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr2:172543771-172544212	K562	blood:	n/a	n/a
15	ATF3	chr2:172544078-172544734	K562	blood:	n/a	chr2:172544372-172544381
16	ATF3	chr2:172543767-172544095	HepG2	liver:	n/a	n/a
17	BATF	chr2:172508950-172509189	GM12878	blood:	n/a	chr2:172509081-172509092
18	BATF	chr2:172508961-172509161	GM12878	blood:	n/a	chr2:172509081-172509092
19	BCL3	chr2:172543676-172544538	A549	lung:	n/a	chr2:172544519-172544528
20	BCLAF1	chr2:172543676-172544508	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:172543671-172544801	K562	blood:	n/a	n/a
22	BHLHE40	chr2:172455318-172455600	GM12878	blood:	n/a	n/a
23	BHLHE40	chr2:172545232-172545316	K562	blood:	n/a	n/a
24	BHLHE40	chr2:172487630-172488028	K562	blood:	n/a	n/a
25	BHLHE40	chr2:172543750-172544458	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:172543222-172543268	K562	blood:	n/a	n/a
27	BHLHE40	chr2:172457467-172457593	K562	blood:	n/a	n/a
28	BHLHE40	chr2:172452671-172452845	K562	blood:	n/a	n/a
29	BRCA1	chr2:172544303-172544404	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr2:172543678-172544448	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr2:172459657-172459751	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr2:172487573-172488289	K562	blood:	n/a	n/a
33	CBX3	chr2:172483320-172483868	K562	blood:	n/a	n/a
34	CBX3	chr2:172487792-172488338	HCT-116	colon:	n/a	n/a
35	CBX3	chr2:172487582-172488291	K562	blood:	n/a	n/a
36	CBX3	chr2:172508283-172508477	K562	blood:	n/a	n/a
37	CBX3	chr2:172543546-172544959	K562	blood:	n/a	n/a
38	CBX3	chr2:172487776-172488341	HCT-116	colon:	n/a	n/a
39	CBX3	chr2:172508206-172508529	K562	blood:	n/a	n/a
40	CBX3	chr2:172543618-172544354	K562	blood:	n/a	n/a
41	CBX3	chr2:172483438-172483828	K562	blood:	n/a	n/a
42	CCNT2	chr2:172544347-172544656	K562	blood:	n/a	n/a
43	CCNT2	chr2:172487755-172487990	K562	blood:	n/a	n/a
44	CEBPB	chr2:172486081-172486378	IMR90	lung:	n/a	chr2:172486228-172486239
45	CEBPB	chr2:172486224-172486251	H1-hESC	embryonic stem cell:	n/a	chr2:172486228-172486239
46	CEBPB	chr2:172530539-172530741	K562	blood:	n/a	chr2:172530600-172530611 chr2:172530637-172530650 chr2:172530600-172530613
47	CEBPB	chr2:172455320-172455590	A549	lung:	n/a	n/a
48	CEBPB	chr2:172444188-172444350	Hela-S3	cervix:	n/a	chr2:172444268-172444277 chr2:172444267-172444278 chr2:172444204-172444215 chr2:172444205-172444214 chr2:172444266-172444279 chr2:172444266-172444277
49	CEBPB	chr2:172516410-172516700	HepG2	liver:	n/a	chr2:172516543-172516554
50	CEBPB	chr2:172452365-172452771	IMR90	lung:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:172543902-172543952	HRCEpiC	kidney:	n/a
2	chr2:172542111-172542161	AoSMC	blood vessel:	n/a
3	chr2:172543902-172543952	HRCEpiC	kidney:	n/a
4	chr2:172542111-172542161	AoSMC	blood vessel:	n/a
5	chr2:172543902-172543952	HMEC	breast:	n/a
6	chr2:172543808-172543858	HRE	kidney:	n/a
7	chr2:172544429-172544479	PrEC	prostate:	n/a
8	chr2:172452502-172452552	NHBE	bronchial:	n/a
9	chr2:172452502-172452552	AG09309	skin:	n/a
10	chr2:172542111-172542161	AG09309	skin:	n/a
11	chr2:172543902-172543952	AG09309	skin:	n/a
12	chr2:172524214-172524264	HRCEpiC	kidney:	n/a
13	chr2:172543808-172543858	HIPEpiC	eye:	n/a
14	chr2:172543677-172543727	GM06990	blood:	n/a
15	chr2:172543677-172543727	HIPEpiC	eye:	n/a
16	chr2:172546870-172546920	A549	lung:	n/a
17	chr2:172452502-172452552	SK-N-SH	brain:	n/a
18	chr2:172452502-172452552	ProgFib	skin:	n/a
19	chr2:172544446-172544496	HEK293	kidney:	embryo
20	chr2:172544429-172544479	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:172542111-172542161	Hela-S3	cervix:	n/a
22	chr2:172543905-172543955	HEK293	kidney:	embryo
23	chr2:172544429-172544479	GM06990	blood:	n/a
24	chr2:172546870-172546920	K562	blood:	n/a
25	chr2:172546870-172546920	HEEpiC	esophagus:	n/a
26	chr2:172542111-172542161	T-47D	breast:	n/a
27	chr2:172544429-172544479	Hela-S3	cervix:	n/a
28	chr2:172452502-172452552	AG04449	skin:	fetal
29	chr2:172544446-172544496	SAEC	small airway:	n/a
30	chr2:172544336-172544386	HEK293	kidney:	embryo
31	chr2:172546870-172546920	CMK	blood:	n/a
32	chr2:172541622-172541672	GM12891	blood:	n/a
33	chr2:172544429-172544479	BJ	skin:	n/a
34	chr2:172544069-172544119	AoSMC	blood vessel:	n/a
35	chr2:172544429-172544479	HepG2	liver:	n/a
36	chr2:172543834-172543884	K562	blood:	n/a
37	chr2:172541622-172541672	HRE	kidney:	n/a
38	chr2:172543902-172543952	HL-60	blood:	n/a
39	chr2:172541622-172541672	AG10803	skin:	n/a
40	chr2:172452502-172452552	HEEpiC	esophagus:	n/a
41	chr2:172546870-172546920	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:172543946-172543996	NT2-D1	testis:	n/a
43	chr2:172543905-172543955	HCT-116	colon:	n/a
44	chr2:172544069-172544119	HCT-116	colon:	n/a
45	chr2:172543677-172543727	GM12878	blood:	n/a
46	chr2:172543834-172543884	AG04450	lung:	fetal
47	chr2:172543834-172543884	ovcar-3	ovarian:	n/a
48	chr2:172543743-172543793	PrEC	prostate:	n/a
49	chr2:172544773-172544823	HAEpiC	amniotic membrane:	n/a
50	chr2:172544773-172544823	HEEpiC	esophagus:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:172543765..172545467-chr2:172749369..172751686,2	MCF-7	breast:
2	chr2:172525954..172528530-chr2:172530857..172533373,2	MCF-7	breast:
3	chr2:172528852..172530373-chr2:172530761..172532541,2	MCF-7	breast:
4	chr2:172454943..172455628-chr2:172559838..172560666,2	MCF-7	breast:
5	chr2:172377472..172379940-chr2:172439801..172442864,3	K562	blood:
6	chr2:172457790..172459885-chr2:172470961..172473294,2	K562	blood:
7	chr2:172450683..172452462-chr2:172537710..172539428,2	K562	blood:
8	chr19:13049203..13049816-chr2:172543937..172544636,2	Hela-S3	cervix:
9	chr2:172440684..172442234-chr2:172455013..172456905,2	MCF-7	breast:
10	chr2:172528585..172533406-chr2:172536831..172539990,4	K562	blood:
11	chr2:172526794..172530696-chr2:172532860..172536577,3	K562	blood:
12	chr2:172440684..172442234-chr2:172455013..172456905,2	MCF-7	breast:
13	chr2:172454209..172457044-chr2:172571141..172573301,2	MCF-7	breast:
14	chr2:172508719..172510692-chr2:172541711..172543434,2	MCF-7	breast:
15	chr2:172531431..172533779-chr2:172542389..172544268,2	K562	blood:
16	chr1:11967533..11969732-chr2:172535151..172536653,2	MCF-7	breast:
17	chr2:172463472..172465048-chr2:172466718..172469351,2	K562	blood:
18	chr2:172443186..172445133-chr2:172451664..172453720,2	K562	blood:
19	chr2:172454943..172455628-chr2:172559838..172560666,2	MCF-7	breast:
20	chr2:172515976..172517510-chr2:172543277..172545672,3	K562	blood:
21	chr2:172535813..172538723-chr2:172541554..172544032,2	MCF-7	breast:
22	chr2:172542927..172544505-chr2:172566367..172569318,2	K562	blood:
23	chr2:172454934..172455567-chr2:172559837..172560822,3	MCF-7	breast:
24	chr2:172554984..172557454-chr2:172560773..172563069,2	K562	blood:
25	chr2:172536408..172538619-chr2:172539945..172541778,2	MCF-7	breast:
26	chr2:172557694..172560489-chr2:172560501..172562511,2	K562	blood:
27	chr2:172441930..172443679-chr2:172445766..172448276,2	K562	blood:
28	chr2:172544464..172546143-chr2:172776960..172779046,3	K562	blood:
29	chr2:172558785..172561244-chr2:172563256..172565056,2	K562	blood:
30	chr2:172432492..172434881-chr2:172445947..172448436,2	K562	blood:
31	chr2:172502107..172505045-chr2:172508679..172510845,2	K562	blood:
32	chr2:172528585..172533406-chr2:172536831..172539990,4	K562	blood:
33	chr2:172559867..172560730-chr2:172968303..172969236,3	K562	blood:
34	chr2:172560229..172560733-chr2:172991740..172992317,2	MCF-7	breast:
35	chr2:172487381..172489786-chr2:172492244..172493876,2	MCF-7	breast:
36	chr2:172457790..172459885-chr2:172470961..172473294,2	K562	blood:
37	chr2:172485890..172488054-chr2:172488273..172490180,2	MCF-7	breast:
38	chr2:172454934..172455567-chr2:172559837..172560822,3	MCF-7	breast:
39	chr2:172524778..172526890-chr2:172542769..172545112,2	K562	blood:
40	chr2:172558785..172561475-chr2:172562570..172565056,4	K562	blood:
41	chr2:172550811..172553362-chr2:172778656..172780423,2	MCF-7	breast:
42	chr2:172528852..172530373-chr2:172530761..172532541,2	MCF-7	breast:
43	chr2:172558563..172561388-chr2:172862907..172864950,2	K562	blood:
44	chr2:172450683..172452462-chr2:172537710..172539428,2	K562	blood:
45	chr17:59488177..59489729-chr2:172472876..172474445,2	MCF-7	breast:
46	chr2:172522193..172524881-chr2:172526221..172528057,2	K562	blood:
47	chr2:172525954..172528530-chr2:172530857..172533373,2	MCF-7	breast:
48	chr2:172508719..172510692-chr2:172541711..172543434,2	MCF-7	breast:
49	chr2:172522935..172524881-chr2:172525131..172528057,2	K562	blood:
50	chr2:172559872..172560770-chr2:173574898..173575445,2	K562	blood:

No data

Variant related genes	Relation type
RPL21P38	TF binding region
DYNC1I2	TF binding region
RPL21P38	CpG island
DYNC1I2	CpG island
ENSG00000233934	chromatin interactions
ENSG00000123600	chromatin interactions
ENSG00000172878	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000071967	chromatin interactions
ENSG00000179218	chromatin interactions
ENSG00000115827	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000115840	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000128708	chromatin interactions
ENSG00000077380	chromatin interactions
ENSG00000268821	chromatin interactions

Extended variants
information (count: 3711 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:3711 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551639531	chr2:172442243-172442244	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs372766246	chr2:172442244-172442245	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190655520	chr2:172442254-172442255	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375075324	chr2:172442268-172442269	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144337559	chr2:172442317-172442318	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565310974	chr2:172442350-172442351	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534323532	chr2:172442352-172442353	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148808996	chr2:172442353-172442354	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142437257	chr2:172442364-172442365	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs554686116	chr2:172442376-172442377	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573023143	chr2:172442392-172442393	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs183225313	chr2:172442404-172442405	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566902240	chr2:172442419-172442420	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs376841911	chr2:172442454-172442455	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs147881949	chr2:172442455-172442456	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs139831348	chr2:172442473-172442474	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs544468197	chr2:172442481-172442482	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs145340824	chr2:172442530-172442531	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs79903112	chr2:172442539-172442540	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs541649639	chr2:172442542-172442543	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560209027	chr2:172442613-172442614	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs78221949	chr2:172442665-172442666	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539938103	chr2:172442717-172442718	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs187580438	chr2:172442745-172442746	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531626178	chr2:172442753-172442754	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190714254	chr2:172442773-172442774	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375946640	chr2:172442798-172442799	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs115391836	chr2:172442843-172442844	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577000444	chr2:172442844-172442845	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548052506	chr2:172442888-172442889	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs566287142	chr2:172442891-172442892	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs1473995	chr2:172442904-172442905	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs372510653	chr2:172442942-172442943	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs147700392	chr2:172442963-172442964	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs576738138	chr2:172442966-172442967	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs140987818	chr2:172442979-172442980	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs556016226	chr2:172443012-172443013	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs566506776	chr2:172443043-172443044	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs574437633	chr2:172443062-172443063	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs114913545	chr2:172443101-172443102	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs559872237	chr2:172443118-172443119	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs115754229	chr2:172443153-172443154	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs527369580	chr2:172443193-172443194	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs182914735	chr2:172443213-172443214	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs73979406	chr2:172443263-172443264	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs531712853	chr2:172443265-172443266	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs76489408	chr2:172443292-172443293	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs187876452	chr2:172443343-172443344	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs562361964	chr2:172443353-172443354	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs190257876	chr2:172443387-172443388	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

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
Intellectual disability	22102821	CNVD
Cancer	20164919	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
Seminomas	18059402	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
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172439800-172442800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr2:172440800-172442600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr2:172442200-172443400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr2:172442600-172442800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:172442800-172443400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:172443400-172443800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:172443400-172443800	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr2:172443400-172445600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr2:172443400-172448400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:172443800-172444000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:172443800-172444400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr2:172444000-172444600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:172444400-172444800	Active TSS	Monocytes-CD14+_RO01746	blood
14	chr2:172444600-172448400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:172444800-172445000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr2:172445000-172445600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr2:172447000-172447200	ZNF genes & repeats	HSMMtube	muscle
18	chr2:172447200-172452000	Weak transcription	HSMMtube	muscle
19	chr2:172448200-172448400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr2:172448200-172448800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr2:172448200-172449000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr2:172448400-172448600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:172448400-172448600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:172448400-172448600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr2:172448400-172448800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr2:172448400-172448800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr2:172448400-172448800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:172448400-172449000	Active TSS	Osteobl	bone
29	chr2:172448400-172449200	Enhancers	Fetal Lung	lung
30	chr2:172448600-172448800	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:172448600-172448800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:172448600-172448800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr2:172448600-172448800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr2:172448600-172448800	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr2:172448600-172448800	Bivalent Enhancer	NHDF-Ad	bronchial
36	chr2:172448600-172448800	Flanking Bivalent TSS/Enh	NHLF	lung
37	chr2:172448600-172449000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:172448600-172449000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr2:172448600-172449000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr2:172448600-172449000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:172448600-172449000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr2:172448600-172449000	Active TSS	Adipose Nuclei	Adipose
43	chr2:172448600-172449000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr2:172448600-172449000	Active TSS	Right Atrium	heart
45	chr2:172448600-172449200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr2:172448600-172449200	Enhancers	Gastric	stomach
47	chr2:172448800-172449000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:172448800-172449000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr2:172448800-172452000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr2:172449000-172449200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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