Variant report

Variant	nsv961690
Chromosome Location	chr2:54339295-54359290
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:834)
CpG islands
(count:549)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:834 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:54348943-54349803	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:54342214-54342674	K562	blood:	n/a	n/a
3	ARID3A	chr2:54342112-54343329	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:54350062-54350502	HepG2	liver:	n/a	n/a
5	ATF1	chr2:54350171-54350540	K562	blood:	n/a	n/a
6	ATF2	chr2:54342597-54343101	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:54342259-54343435	GM12878	blood:	n/a	n/a
8	ATF2	chr2:54342653-54343101	GM12878	blood:	n/a	n/a
9	ATF2	chr2:54342739-54343162	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr2:54342441-54343319	A549	lung:	n/a	chr2:54342686-54342706
11	ATF3	chr2:54342494-54343241	A549	lung:	n/a	chr2:54342686-54342706
12	ATF3	chr2:54342491-54342880	K562	blood:	n/a	chr2:54342686-54342706
13	BACH1	chr2:54344004-54344187	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:54342641-54343194	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr2:54342290-54342469	K562	blood:	n/a	n/a
16	BACH1	chr2:54342909-54343140	K562	blood:	n/a	n/a
17	BCL3	chr2:54342350-54343391	A549	lung:	n/a	chr2:54343027-54343036 chr2:54343022-54343035
18	BCL3	chr2:54342363-54343384	A549	lung:	n/a	chr2:54343027-54343036 chr2:54343022-54343035
19	BCLAF1	chr2:54342302-54343327	GM12878	blood:	n/a	chr2:54343027-54343036 chr2:54343022-54343035
20	BCLAF1	chr2:54342532-54343140	K562	blood:	n/a	chr2:54343027-54343036 chr2:54343022-54343035
21	BCLAF1	chr2:54342382-54343284	GM12878	blood:	n/a	chr2:54343027-54343036 chr2:54343022-54343035
22	BHLHE40	chr2:54351871-54352015	K562	blood:	n/a	n/a
23	BHLHE40	chr2:54342457-54343261	HepG2	liver:	n/a	chr2:54343156-54343172 chr2:54343022-54343038
24	BHLHE40	chr2:54342339-54343334	K562	blood:	n/a	chr2:54343156-54343172 chr2:54343022-54343038
25	BHLHE40	chr2:54350178-54350387	HepG2	liver:	n/a	n/a
26	BHLHE40	chr2:54342489-54343344	GM12878	blood:	n/a	chr2:54343156-54343172 chr2:54343022-54343038
27	BRCA1	chr2:54342560-54343076	GM12878	blood:	n/a	n/a
28	BRCA1	chr2:54342273-54343384	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr2:54342460-54343144	HepG2	liver:	n/a	n/a
30	BRCA1	chr2:54342604-54342752	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr2:54342721-54343433	K562	blood:	n/a	n/a
32	CBX3	chr2:54348068-54348581	K562	blood:	n/a	n/a
33	CBX3	chr2:54343541-54344165	HCT-116	colon:	n/a	n/a
34	CBX3	chr2:54343593-54344066	K562	blood:	n/a	n/a
35	CBX3	chr2:54342478-54344313	K562	blood:	n/a	n/a
36	CCNT2	chr2:54342484-54343202	K562	blood:	n/a	n/a
37	CEBPB	chr2:54342363-54343239	H1-hESC	embryonic stem cell:	n/a	chr2:54342374-54342385
38	CEBPB	chr2:54353992-54354196	K562	blood:	n/a	n/a
39	CEBPB	chr2:54342278-54342566	IMR90	lung:	n/a	chr2:54342338-54342349 chr2:54342374-54342385
40	CEBPB	chr2:54343776-54344021	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr2:54342213-54342556	A549	lung:	n/a	chr2:54342338-54342349 chr2:54342374-54342385
42	CEBPB	chr2:54342212-54343098	Hela-S3	cervix:	n/a	chr2:54342338-54342349 chr2:54342374-54342385
43	CEBPB	chr2:54342230-54342536	HepG2	liver:	n/a	chr2:54342338-54342349 chr2:54342374-54342385
44	CEBPB	chr2:54342212-54342570	K562	blood:	n/a	chr2:54342338-54342349 chr2:54342374-54342385
45	CEBPD	chr2:54342500-54343299	HepG2	liver:	n/a	n/a
46	CEBPD	chr2:54342588-54343256	HepG2	liver:	n/a	n/a
47	CHD1	chr2:54342377-54343177	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr2:54342426-54343266	GM12878	blood:	n/a	n/a
49	CHD1	chr2:54341903-54343457	IMR90	lung:	n/a	n/a
50	CHD2	chr2:54342376-54343307	GM12878	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:54340934-54340984	HMEC	breast:	n/a
2	chr2:54340934-54340984	PrEC	prostate:	n/a
3	chr2:54342961-54343011	PrEC	prostate:	n/a
4	chr2:54340298-54340348	SK-N-MC	brain:	n/a
5	chr2:54342651-54342701	H1-hESC	embryonic stem cell:	embryo
6	chr2:54345792-54345842	MCF10A-Er-Src	breast:	n/a
7	chr2:54342651-54342701	HCM	heart:	n/a
8	chr2:54350432-54350482	HUVEC	blood vessel:	n/a
9	chr2:54342806-54342856	AG09309	skin:	n/a
10	chr2:54342961-54343011	K562	blood:	n/a
11	chr2:54342584-54342634	HL-60	blood:	n/a
12	chr2:54340298-54340348	AG04449	skin:	fetal
13	chr2:54343179-54343229	NH-A	brain:	n/a
14	chr2:54342584-54342634	T-47D	breast:	n/a
15	chr2:54342961-54343011	IMR90	lung:	fetal
16	chr2:54343179-54343229	PFSK-1	brain:	n/a
17	chr2:54343179-54343229	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:54342651-54342701	PANC-1	pancreas:	n/a
19	chr2:54345792-54345842	GM12891	blood:	n/a
20	chr2:54343179-54343229	SK-N-SH_RA	brain:	n/a
21	chr2:54342806-54342856	HMEC	breast:	n/a
22	chr2:54342651-54342701	GM12891	blood:	n/a
23	chr2:54342584-54342634	IMR90	lung:	fetal
24	chr2:54340298-54340348	MCF10A-Er-Src	breast:	n/a
25	chr2:54350432-54350482	H1-hESC	embryonic stem cell:	embryo
26	chr2:54342806-54342856	HL-60	blood:	n/a
27	chr2:54342806-54342856	GM12878	blood:	n/a
28	chr2:54342651-54342701	K562	blood:	n/a
29	chr2:54345792-54345842	HCT-116	colon:	n/a
30	chr2:54342961-54343011	ovcar-3	ovarian:	n/a
31	chr2:54343179-54343229	AG09319	gingival:	n/a
32	chr2:54345792-54345842	HMEC	breast:	n/a
33	chr2:54342806-54342856	MCF10A-Er-Src	breast:	n/a
34	chr2:54350432-54350482	HEEpiC	esophagus:	n/a
35	chr2:54342584-54342634	PFSK-1	brain:	n/a
36	chr2:54340934-54340984	HRPEpiC	eye:	n/a
37	chr2:54342584-54342634	HCT-116	colon:	n/a
38	chr2:54342651-54342701	CMK	blood:	n/a
39	chr2:54342806-54342856	HepG2	liver:	n/a
40	chr2:54340934-54340984	SKMC	muscle:	n/a
41	chr2:54340934-54340984	Hela-S3	cervix:	n/a
42	chr2:54343179-54343229	GM06990	blood:	n/a
43	chr2:54343179-54343229	A549	lung:	n/a
44	chr2:54342584-54342634	GM12892	blood:	n/a
45	chr2:54342806-54342856	AG04449	skin:	fetal
46	chr2:54340934-54340984	NT2-D1	testis:	n/a
47	chr2:54350432-54350482	IMR90	lung:	fetal
48	chr2:54342651-54342701	HepG2	liver:	n/a
49	chr2:54345792-54345842	HEEpiC	esophagus:	n/a
50	chr2:54345792-54345842	AG09309	skin:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:20912054..20912881-chr2:54342309..54343237,2	Hela-S3	cervix:
2	chr2:54353860..54357435-chr2:54358249..54361624,3	K562	blood:
3	chr2:54333529..54340855-chr2:54341009..54344742,14	K562	blood:
4	chr2:54341176..54343229-chr2:54346629..54349067,2	K562	blood:
5	chr2:54342236..54343923-chr2:54879380..54882162,2	MCF-7	breast:
6	chr2:54335252..54336789-chr2:54355206..54357354,2	MCF-7	breast:
7	chr2:54343136..54344762-chr2:54350422..54352755,2	K562	blood:
8	chr2:54342079..54343052-chr5:109024930..109025777,2	Hela-S3	cervix:
9	chr2:54341515..54343973-chr2:55337394..55340042,2	MCF-7	breast:
10	chr17:79849578..79850209-chr2:54342411..54343037,2	Hela-S3	cervix:
11	chr2:54319207..54320818-chr2:54338574..54340927,2	K562	blood:
12	chr2:54341307..54344135-chr2:54557168..54559182,2	K562	blood:
13	chr2:54341659..54344698-chr2:54352246..54354996,3	MCF-7	breast:
14	chr2:54342420..54344092-chr20:46285600..46287785,2	MCF-7	breast:
15	chr2:54352052..54355360-chr2:54358848..54360965,3	K562	blood:
16	chr2:54356754..54359012-chr2:54361196..54364127,2	K562	blood:
17	chr19:48281526..48282040-chr2:54342571..54343371,2	NB4	blood:
18	chr2:54334014..54340621-chr2:54341231..54344595,11	MCF-7	breast:
19	chr2:54341216..54345253-chr2:54347980..54351307,5	MCF-7	breast:
20	chr2:54353860..54357435-chr2:54358249..54361624,3	K562	blood:
21	chr2:54340543..54343083-chr2:54350579..54352338,2	K562	blood:
22	chr15:76603595..76604138-chr2:54342354..54343006,2	HCT-116	colon:
23	chr2:54341795..54343300-chr2:54353986..54355682,2	K562	blood:
24	chr2:54343141..54345901-chr2:54421855..54423562,2	K562	blood:
25	chr2:54343136..54344762-chr2:54350422..54352755,2	K562	blood:
26	chr2:54341176..54344555-chr2:54346430..54350020,7	K562	blood:
27	chr2:54341520..54343821-chr2:54682367..54684141,3	MCF-7	breast:
28	chr2:54341806..54344770-chr2:54784235..54787039,2	MCF-7	breast:
29	chr2:54348914..54351934-chr2:54354542..54358580,3	K562	blood:
30	chr2:54294456..54296366-chr2:54347167..54348766,2	K562	blood:
31	chr2:54196743..54198781-chr2:54341566..54344110,2	K562	blood:
32	chr2:54340617..54344494-chr2:54480899..54484108,3	K562	blood:
33	chr2:54341443..54343043-chr2:54557751..54559883,2	MCF-7	breast:
34	chr2:54352052..54355360-chr2:54358848..54360965,3	K562	blood:
35	chr2:54341216..54345253-chr2:54347980..54351307,5	MCF-7	breast:
36	chr2:54316468..54319152-chr2:54339625..54341327,2	K562	blood:
37	chr2:54195752..54197966-chr2:54347709..54349839,3	K562	blood:
38	chr18:12947857..12948364-chr2:54342415..54343083,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
ACYP2	TF binding region
ACYP2	CpG island
ENSG00000140374	chromatin interactions
ENSG00000085415	chromatin interactions
ENSG00000178021	chromatin interactions
ENSG00000068878	chromatin interactions
ENSG00000178980	chromatin interactions
ENSG00000170634	chromatin interactions
ENSG00000177994	chromatin interactions
ENSG00000112893	chromatin interactions
ENSG00000141552	chromatin interactions
ENSG00000115306	chromatin interactions
ENSG00000102897	chromatin interactions
ENSG00000196562	chromatin interactions
ENSG00000115310	chromatin interactions

Extended variants
information (count: 950 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:950 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190166293	chr2:54339358-54339359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs535794167	chr2:54339369-54339370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs58371916	chr2:54339407-54339408	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548238587	chr2:54339474-54339475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs143790632	chr2:54339481-54339482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112853670	chr2:54339503-54339504	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs148214950	chr2:54339525-54339526	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs551028676	chr2:54339533-54339534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs4671857	chr2:54339535-54339536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs180959436	chr2:54339571-54339572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs151232013	chr2:54339576-54339577	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs374018922	chr2:54339577-54339578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574408437	chr2:54339617-54339618	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552967664	chr2:54339632-54339633	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs7561836	chr2:54339633-54339634	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs535605356	chr2:54339743-54339744	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375085573	chr2:54339763-54339764	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185186677	chr2:54339764-54339765	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs111328968	chr2:54339767-54339768	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs62137980	chr2:54339769-54339770	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs543600279	chr2:54339791-54339792	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs563427962	chr2:54339819-54339820	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7562055	chr2:54339831-54339832	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs546084605	chr2:54339875-54339876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559411679	chr2:54339958-54339959	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559758192	chr2:54339970-54339971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528070422	chr2:54339971-54339972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141221906	chr2:54339979-54339980	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191038971	chr2:54339981-54339982	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531056980	chr2:54339988-54339989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs551154921	chr2:54339994-54339995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113908757	chr2:54340001-54340002	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570670234	chr2:54340048-54340049	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552698509	chr2:54340051-54340052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539767411	chr2:54340062-54340063	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs150748778	chr2:54340136-54340137	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs138281291	chr2:54340152-54340153	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs370187169	chr2:54340153-54340154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566563664	chr2:54340155-54340156	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs137872787	chr2:54340171-54340172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562003445	chr2:54340177-54340178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs374939753	chr2:54340214-54340215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs562339370	chr2:54340221-54340222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs369105283	chr2:54340246-54340247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555627651	chr2:54340259-54340260	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371621904	chr2:54340260-54340261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537912481	chr2:54340339-54340340	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs557210200	chr2:54340359-54340360	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs60452262	chr2:54340378-54340379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111776995	chr2:54340408-54340409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:54291200-54342000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr2:54331200-54342000	Weak transcription	Psoas Muscle	Psoas
3	chr2:54331200-54342400	Weak transcription	Pancreas	Pancrea
4	chr2:54331400-54342200	Weak transcription	Aorta	Aorta
5	chr2:54333800-54341800	Weak transcription	K562	blood
6	chr2:54334800-54341600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:54334800-54341800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:54334800-54342000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr2:54335200-54341200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:54335600-54341800	Weak transcription	Fetal Heart	heart
11	chr2:54335800-54341200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr2:54335800-54341200	Weak transcription	Brain Substantia Nigra	brain
13	chr2:54335800-54341800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr2:54335800-54341800	Weak transcription	HSMM	muscle
15	chr2:54335800-54341800	Weak transcription	HSMMtube	muscle
16	chr2:54335800-54342000	Weak transcription	Fetal Muscle Leg	muscle
17	chr2:54336000-54341400	Weak transcription	Fetal Brain Male	brain
18	chr2:54336000-54341800	Weak transcription	Primary B cells from cord blood	blood
19	chr2:54336000-54341800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:54336000-54341800	Weak transcription	Brain Angular Gyrus	brain
21	chr2:54336000-54341800	Weak transcription	Brain Anterior Caudate	brain
22	chr2:54336000-54341800	Weak transcription	Brain Hippocampus Middle	brain
23	chr2:54336000-54341800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr2:54336000-54341800	Weak transcription	HMEC	breast
25	chr2:54336000-54342000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr2:54336000-54342000	Weak transcription	NHEK	skin
27	chr2:54340200-54341400	Weak transcription	HepG2	liver
28	chr2:54340800-54341200	Enhancers	Dnd41	blood
29	chr2:54341200-54341600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:54341200-54341800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:54341200-54341800	Enhancers	Brain Substantia Nigra	brain
32	chr2:54341200-54342200	Flanking Active TSS	Dnd41	blood
33	chr2:54341400-54341800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:54341400-54341800	Enhancers	Fetal Brain Male	brain
35	chr2:54341400-54342000	Enhancers	HepG2	liver
36	chr2:54341600-54341800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr2:54341600-54341800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:54341600-54341800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:54341600-54341800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr2:54341600-54341800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:54341600-54341800	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr2:54341600-54341800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr2:54341600-54342000	Enhancers	Liver	Liver
44	chr2:54341600-54342000	Enhancers	Fetal Thymus	thymus
45	chr2:54341600-54342000	Active TSS	Rectal Smooth Muscle	rectum
46	chr2:54341600-54342000	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr2:54341600-54342200	Enhancers	Primary T cells fromperipheralblood	blood
48	chr2:54341600-54342200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr2:54341600-54342200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr2:54341600-54342400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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