Variant report

Variant	nsv833814
Chromosome Location	chr2:37643132-37840247
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2532)
CpG islands
(count:733)
Chromatin interactive
region (count:73)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2532 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37791509-37791839	K562	blood:	n/a	n/a
2	ARID3A	chr2:37788399-37789814	K562	blood:	n/a	n/a
3	ARID3A	chr2:37813485-37813599	K562	blood:	n/a	n/a
4	ATF1	chr2:37683295-37683405	K562	blood:	n/a	n/a
5	ATF1	chr2:37788766-37789778	K562	blood:	n/a	n/a
6	ATF1	chr2:37688108-37688338	K562	blood:	n/a	n/a
7	ATF1	chr2:37785928-37786123	K562	blood:	n/a	n/a
8	ATF1	chr2:37680213-37680384	K562	blood:	n/a	n/a
9	ATF1	chr2:37751020-37751314	K562	blood:	n/a	n/a
10	ATF1	chr2:37813344-37813675	K562	blood:	n/a	n/a
11	ATF1	chr2:37795814-37796120	K562	blood:	n/a	n/a
12	ATF1	chr2:37652581-37652908	K562	blood:	n/a	n/a
13	ATF2	chr2:37777167-37777705	GM12878	blood:	n/a	n/a
14	ATF2	chr2:37772609-37773228	GM12878	blood:	n/a	n/a
15	ATF2	chr2:37776602-37777831	GM12878	blood:	n/a	n/a
16	ATF2	chr2:37797556-37799195	GM12878	blood:	n/a	chr2:37798092-37798099
17	ATF2	chr2:37813152-37813759	GM12878	blood:	n/a	n/a
18	ATF2	chr2:37785796-37786291	GM12878	blood:	n/a	n/a
19	ATF2	chr2:37772606-37773191	GM12878	blood:	n/a	n/a
20	ATF2	chr2:37733520-37733938	GM12878	blood:	n/a	n/a
21	ATF2	chr2:37785747-37786347	GM12878	blood:	n/a	n/a
22	ATF2	chr2:37827809-37828379	GM12878	blood:	n/a	n/a
23	ATF2	chr2:37800861-37801410	GM12878	blood:	n/a	n/a
24	ATF2	chr2:37797402-37799149	GM12878	blood:	n/a	chr2:37798092-37798099
25	ATF2	chr2:37801045-37801610	GM12878	blood:	n/a	n/a
26	ATF3	chr2:37788816-37789002	GM12878	blood:	n/a	n/a
27	ATF3	chr2:37788706-37789086	GM12878	blood:	n/a	n/a
28	ATF3	chr2:37788765-37789063	K562	blood:	n/a	n/a
29	ATF3	chr2:37789375-37789814	K562	blood:	n/a	n/a
30	ATF3	chr2:37788654-37789254	K562	blood:	n/a	n/a
31	BACH1	chr2:37788843-37789230	K562	blood:	n/a	n/a
32	BATF	chr2:37829880-37830187	GM12878	blood:	n/a	n/a
33	BATF	chr2:37829881-37830169	GM12878	blood:	n/a	n/a
34	BATF	chr2:37827908-37828305	GM12878	blood:	n/a	chr2:37828080-37828091 chr2:37828085-37828095
35	BATF	chr2:37813371-37813678	GM12878	blood:	n/a	n/a
36	BATF	chr2:37733579-37733877	GM12878	blood:	n/a	chr2:37733764-37733775
37	BATF	chr2:37668219-37668493	GM12878	blood:	n/a	n/a
38	BATF	chr2:37675000-37675224	GM12878	blood:	n/a	n/a
39	BATF	chr2:37785888-37786232	GM12878	blood:	n/a	n/a
40	BATF	chr2:37797828-37798717	GM12878	blood:	n/a	chr2:37798392-37798401
41	BATF	chr2:37829221-37829480	GM12878	blood:	n/a	n/a
42	BATF	chr2:37827898-37828213	GM12878	blood:	n/a	chr2:37828080-37828091 chr2:37828085-37828095
43	BATF	chr2:37668968-37669292	GM12878	blood:	n/a	n/a
44	BATF	chr2:37797887-37798681	GM12878	blood:	n/a	chr2:37798392-37798401
45	BATF	chr2:37760165-37760345	GM12878	blood:	n/a	chr2:37760272-37760283
46	BCL11A	chr2:37785918-37786184	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:37733525-37733884	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:37797816-37798669	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:37827971-37828206	GM12878	blood:	n/a	chr2:37828084-37828093 chr2:37828083-37828092
50	BCL11A	chr2:37797919-37798609	GM12878	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37790618-37790668	AG04450	lung:	fetal
2	chr2:37790618-37790668	AG04450	lung:	fetal
3	chr2:37663730-37663780	GM06990	blood:	n/a
4	chr2:37815128-37815178	AG04449	skin:	fetal
5	chr2:37798344-37798394	HRPEpiC	eye:	n/a
6	chr2:37663730-37663780	HCF	heart:	n/a
7	chr2:37787889-37787939	K562	blood:	n/a
8	chr2:37703400-37703450	BE2_C	brain:	n/a
9	chr2:37790618-37790668	MCF-7	breast:	n/a
10	chr2:37699716-37699766	SK-N-MC	brain:	n/a
11	chr2:37787889-37787939	RPTEC	kidney:	n/a
12	chr2:37790618-37790668	GM12878	blood:	n/a
13	chr2:37663730-37663780	HL-60	blood:	n/a
14	chr2:37813553-37813603	HCM	heart:	n/a
15	chr2:37798344-37798394	HCF	heart:	n/a
16	chr2:37734390-37734440	RPTEC	kidney:	n/a
17	chr2:37703400-37703450	ovcar-3	ovarian:	n/a
18	chr2:37787889-37787939	PrEC	prostate:	n/a
19	chr2:37815128-37815178	HCT-116	colon:	n/a
20	chr2:37663730-37663780	AG04450	lung:	fetal
21	chr2:37813553-37813603	AG10803	skin:	n/a
22	chr2:37815128-37815178	PANC-1	pancreas:	n/a
23	chr2:37815128-37815178	HUVEC	blood vessel:	n/a
24	chr2:37703400-37703450	U87	brain:	n/a
25	chr2:37684473-37684523	ovcar-3	ovarian:	n/a
26	chr2:37734390-37734440	T-47D	breast:	n/a
27	chr2:37787889-37787939	HCM	heart:	n/a
28	chr2:37684473-37684523	PANC-1	pancreas:	n/a
29	chr2:37703400-37703450	PFSK-1	brain:	n/a
30	chr2:37798344-37798394	SK-N-SH	brain:	n/a
31	chr2:37703400-37703450	HEK293	kidney:	embryo
32	chr2:37798344-37798394	ProgFib	skin:	n/a
33	chr2:37815128-37815178	GM12891	blood:	n/a
34	chr2:37751449-37751499	BE2_C	brain:	n/a
35	chr2:37787889-37787939	AG09319	gingival:	n/a
36	chr2:37663730-37663780	AG09319	gingival:	n/a
37	chr2:37699716-37699766	CMK	blood:	n/a
38	chr2:37699716-37699766	NH-A	brain:	n/a
39	chr2:37816339-37816389	GM06990	blood:	n/a
40	chr2:37684473-37684523	SAEC	small airway:	n/a
41	chr2:37815128-37815178	GM19239	blood:	n/a
42	chr2:37699716-37699766	NHBE	bronchial:	n/a
43	chr2:37815128-37815178	GM12878	blood:	n/a
44	chr2:37813553-37813603	NHBE	bronchial:	n/a
45	chr2:37684473-37684523	IMR90	lung:	fetal
46	chr2:37798344-37798394	K562	blood:	n/a
47	chr2:37813553-37813603	U87	brain:	n/a
48	chr2:37734390-37734440	K562	blood:	n/a
49	chr2:37787889-37787939	ovcar-3	ovarian:	n/a
50	chr2:37815128-37815178	SK-N-SH	brain:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:37810267..37812004-chr2:37812621..37814787,2	MCF-7	breast:
2	chr2:37781860..37785625-chr2:37786304..37788972,4	K562	blood:
3	chr2:37816065..37817832-chr2:37818694..37820590,2	MCF-7	breast:
4	chr2:37796095..37797959-chr2:37798225..37800388,2	K562	blood:
5	chr2:37748014..37749874-chr2:37757456..37760173,2	MCF-7	breast:
6	chr2:37791325..37795155-chr2:37795900..37799036,5	K562	blood:
7	chr2:37807890..37810236-chr2:37813003..37815246,2	K562	blood:
8	chr2:37789729..37791788-chr2:37804945..37807693,2	K562	blood:
9	chr2:37839740..37841439-chr2:37842697..37845685,2	K562	blood:
10	chr2:37710296..37713273-chr2:37733233..37735732,2	MCF-7	breast:
11	chr1:149223828..149224363-chr2:37731909..37732409,2	MCF-7	breast:
12	chr2:37789512..37791972-chr2:37800860..37802829,2	K562	blood:
13	chr2:37748769..37750538-chr2:37760905..37763616,2	K562	blood:
14	chr2:37782232..37784356-chr2:37804122..37805641,2	MCF-7	breast:
15	chr2:37682465..37684139-chr2:37686739..37688333,2	K562	blood:
16	chr2:37796095..37797959-chr2:37798225..37800388,2	K562	blood:
17	chr2:37728444..37730701-chr2:37746195..37748553,2	MCF-7	breast:
18	chr2:37678097..37679683-chr2:37681687..37683352,2	K562	blood:
19	chr2:37795029..37797811-chr2:37802354..37805859,3	K562	blood:
20	chr2:37693807..37696751-chr2:37697172..37699448,2	MCF-7	breast:
21	chr2:37748014..37749874-chr2:37757456..37760173,2	MCF-7	breast:
22	chr2:37804698..37807657-chr2:37813185..37814836,2	K562	blood:
23	chr2:37765925..37767453-chr2:37769359..37772141,2	K562	blood:
24	chr2:37636169..37638142-chr2:37642427..37644282,2	K562	blood:
25	chr2:37700411..37701975-chr2:37710008..37711802,2	MCF-7	breast:
26	chr2:37641113..37643147-chr2:38035425..38037693,2	MCF-7	breast:
27	chr2:37810708..37813206-chr2:37814020..37815979,2	K562	blood:
28	chr2:37674288..37676337-chr2:37685737..37688675,2	K562	blood:
29	chr2:37786608..37790547-chr2:37791244..37795872,7	K562	blood:
30	chr2:37781860..37785625-chr2:37786304..37788972,4	K562	blood:
31	chr2:37678097..37679683-chr2:37681687..37683352,2	K562	blood:
32	chr2:37674288..37676337-chr2:37685737..37688675,2	K562	blood:
33	chr2:37807890..37810236-chr2:37813003..37815246,2	K562	blood:
34	chr2:37750494..37753126-chr2:37755282..37758180,2	MCF-7	breast:
35	chr2:37804698..37807657-chr2:37813185..37814836,2	K562	blood:
36	chr2:37728444..37730701-chr2:37746195..37748553,2	MCF-7	breast:
37	chr2:37779367..37783955-chr2:37786259..37791654,6	K562	blood:
38	chr2:37700411..37701975-chr2:37710008..37711802,2	MCF-7	breast:
39	chr2:37667647..37669347-chr2:37672463..37673987,2	K562	blood:
40	chr2:37813986..37816982-chr2:37818783..37822459,3	K562	blood:
41	chr2:37641385..37643169-chr2:38059236..38060312,7	MCF-7	breast:
42	chr2:37682465..37684139-chr2:37686739..37688333,2	K562	blood:
43	chr2:37710296..37713273-chr2:37733233..37735732,2	MCF-7	breast:
44	chr2:37799670..37802467-chr2:37802654..37804539,2	MCF-7	breast:
45	chr2:37810267..37812004-chr2:37812621..37814787,2	MCF-7	breast:
46	chr2:37785013..37788185-chr2:37797266..37800761,3	K562	blood:
47	chr2:37789512..37791972-chr2:37800860..37802829,2	K562	blood:
48	chr2:37828090..37830166-chr2:37831217..37833289,2	K562	blood:
49	chr2:37779367..37783955-chr2:37786259..37791654,6	K562	blood:
50	chr2:37791325..37795155-chr2:37795900..37799036,5	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-QPCT-3	chr2:37826300-37827505	NONHSAT070127
2	lnc-QPCT-3	chr2:37827279-37827505	ENSG00000236213.1
3	lnc-QPCT-3	chr2:37827040-37827505	XLOC_001430
4	lnc-QPCT-3	chr2:37827065-37827505	XLOC_001430
5	lnc-QPCT-2	chr2:37716639-37716724	XLOC_001429
6	lnc-CDC42EP3-4	chr2:37789433-37789882	NONHSAT070125
7	lnc-QPCT-2	chr2:37764138-37764397	XLOC_001429
8	lnc-QPCT-3	chr2:37831452-37831877	XLOC_001430
9	lnc-QPCT-3	chr2:37831452-37831572	NONHSAT070127
10	lnc-QPCT-4	chr2:37824980-37825290	NONHSAT070126
11	lnc-QPCT-3	chr2:37839316-37839401	ENSG00000236213.1
12	lnc-QPCT-3	chr2:37839316-37839573	XLOC_001430
13	lnc-QPCT-3	chr2:37832379-37870742	NONHSAT070127
14	lnc-QPCT-4	chr2:37827621-37827693	NONHSAT070126

No data

Variant related genes	Relation type
RNU6-1116P	TF binding region
ENSG00000236213	TF binding region
RNU6-1116P	CpG island
ENSG00000236213	CpG island
ENSG00000206737	chromatin interactions
LIMCH1	miRNA target sites

Extended variants
information (count: 8777 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:8777 , 50 per page) page: 1 2 3 4 5 6 7 ... 176

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551850393	chr2:37643147-37643148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538341026	chr2:37643194-37643195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191200567	chr2:37643206-37643207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549409576	chr2:37643212-37643213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143387230	chr2:37643219-37643220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs151311911	chr2:37643233-37643234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547050258	chr2:37643336-37643337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376301271	chr2:37643350-37643351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17020719	chr2:37643372-37643373	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539996991	chr2:37643373-37643374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558048703	chr2:37643376-37643377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570366845	chr2:37643389-37643390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs180835120	chr2:37643394-37643395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555800056	chr2:37643409-37643410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574042550	chr2:37643439-37643440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541550989	chr2:37643556-37643557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112158929	chr2:37643566-37643567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140658230	chr2:37643581-37643582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187577338	chr2:37643624-37643625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564118542	chr2:37643644-37643645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71398226	chr2:37643648-37643649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566702340	chr2:37643664-37643665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531548773	chr2:37643690-37643691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145354393	chr2:37643711-37643712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11680914	chr2:37643720-37643721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533747105	chr2:37643729-37643730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542953370	chr2:37643757-37643758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546944740	chr2:37643810-37643811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377103746	chr2:37643816-37643817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79981149	chr2:37643820-37643821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547112375	chr2:37643834-37643835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565796631	chr2:37643861-37643862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs137910095	chr2:37643879-37643880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190959482	chr2:37643912-37643913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570102724	chr2:37643978-37643979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183082368	chr2:37644029-37644030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142374475	chr2:37644127-37644128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567681810	chr2:37644194-37644195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535042208	chr2:37644209-37644210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553074647	chr2:37644221-37644222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140917547	chr2:37644246-37644247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545170094	chr2:37644304-37644305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376492767	chr2:37644354-37644355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115845771	chr2:37644456-37644457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150078693	chr2:37644459-37644460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543328047	chr2:37644463-37644464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576727135	chr2:37644543-37644544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561621638	chr2:37644554-37644555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544064902	chr2:37644577-37644578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs78518064	chr2:37644630-37644631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2624 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37641400-37643200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr2:37641600-37643200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr2:37641600-37643200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr2:37641800-37643200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:37641800-37643200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:37641800-37643200	Enhancers	HUVEC	blood vessel
7	chr2:37641800-37643200	Enhancers	NHDF-Ad	bronchial
8	chr2:37641800-37643400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr2:37641800-37643600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:37641800-37643800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:37641800-37645600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:37642000-37643200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:37642000-37643400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:37642200-37644400	Weak transcription	NH-A	brain
15	chr2:37642200-37649000	Weak transcription	Fetal Lung	lung
16	chr2:37642400-37644200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:37642400-37644400	Weak transcription	HSMMtube	muscle
18	chr2:37642400-37644600	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:37642400-37645600	Enhancers	Fetal Heart	heart
20	chr2:37642400-37648800	Weak transcription	Fetal Kidney	kidney
21	chr2:37642600-37643800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:37642600-37644200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:37642600-37644200	Weak transcription	HSMM	muscle
24	chr2:37642600-37644400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr2:37642600-37648800	Weak transcription	Fetal Stomach	stomach
26	chr2:37642800-37643200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:37642800-37643600	Enhancers	K562	blood
28	chr2:37642800-37644200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:37642800-37644200	Weak transcription	Osteobl	bone
30	chr2:37643000-37643200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:37643000-37648800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr2:37643200-37644200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:37643200-37644200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr2:37643200-37644200	Weak transcription	NHDF-Ad	bronchial
35	chr2:37643200-37644400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:37643200-37646200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr2:37643200-37651200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:37643400-37643800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr2:37643400-37644400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr2:37643800-37645600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:37643800-37645600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:37644200-37644600	Enhancers	HSMM	muscle
43	chr2:37644200-37645200	Enhancers	Muscle Satellite Cultured Cells	--
44	chr2:37644200-37645400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:37644200-37645400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:37644200-37645600	Enhancers	Osteobl	bone
47	chr2:37644200-37645800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr2:37644200-37645800	Enhancers	NHDF-Ad	bronchial
49	chr2:37644200-37647000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:37644400-37644600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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