Variant report

Variant	esv14836
Chromosome Location	chr2:152435775-152463970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:236)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:236 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:152437230-152437561	GM12878	blood:	n/a	n/a
2	BATF	chr2:152447781-152448112	GM12878	blood:	n/a	n/a
3	BATF	chr2:152458334-152458665	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:152447799-152448098	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:152437248-152437547	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:152458352-152458651	GM12878	blood:	n/a	n/a
7	CEBPB	chr2:152443242-152443477	K562	blood:	n/a	n/a
8	CEBPB	chr2:152453747-152454114	K562	blood:	n/a	n/a
9	CEBPB	chr2:152453798-152454061	K562	blood:	n/a	n/a
10	CEBPB	chr2:152443187-152443552	K562	blood:	n/a	n/a
11	CEBPD	chr2:152448226-152448506	K562	blood:	n/a	n/a
12	CTCF	chr2:152448155-152448157	GM10248	blood:	n/a	n/a
13	CTCF	chr2:152437311-152437586	GM10266	blood:	n/a	n/a
14	CTCF	chr2:152458406-152458670	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr2:152447841-152448151	GM10248	blood:	n/a	n/a
16	CTCF	chr2:152448460-152448610	RPTEC	kidney:	n/a	n/a
17	CTCF	chr2:152447721-152448208	A549	lung:	n/a	n/a
18	CTCF	chr2:152447859-152448128	LNCaP	prostate:	n/a	n/a
19	CTCF	chr2:152438771-152438845	GM10248	blood:	n/a	n/a
20	CTCF	chr2:152437270-152437607	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr2:152448240-152448390	HCM	heart:	n/a	n/a
22	CTCF	chr2:152458215-152458321	GM20000	blood:	n/a	n/a
23	CTCF	chr2:152447780-152447930	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr2:152437314-152437388	Gliobla	brain:	n/a	n/a
25	CTCF	chr2:152447858-152447944	A549	lung:	n/a	n/a
26	CTCF	chr2:152437284-152437589	A549	lung:	n/a	n/a
27	CTCF	chr2:152447760-152448171	A549	lung:	n/a	n/a
28	CTCF	chr2:152447855-152448131	GM10266	blood:	n/a	n/a
29	CTCF	chr2:152437298-152437583	LNCaP	prostate:	n/a	n/a
30	CTCF	chr2:152447857-152447958	Gliobla	brain:	n/a	n/a
31	CTCF	chr2:152453898-152453928	Medullo	brain:	n/a	n/a
32	CTCF	chr2:152447780-152447930	AG09309	skin:	n/a	n/a
33	CTCF	chr2:152447720-152447870	HEK293	kidney:	n/a	n/a
34	CTCF	chr2:152443192-152443631	A549	lung:	n/a	n/a
35	CTCF	chr2:152458310-152458695	K562	blood:	n/a	n/a
36	CTCF	chr2:152437303-152437589	GM13977	blood:	n/a	n/a
37	CTCF	chr2:152458407-152458680	LNCaP	prostate:	n/a	n/a
38	CTCF	chr2:152448240-152448390	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr2:152453805-152454059	A549	lung:	n/a	n/a
40	CTCF	chr2:152437303-152437602	Lung_OC	lung:	n/a	n/a
41	CTCF	chr2:152458415-152458693	GM13977	blood:	n/a	n/a
42	CTCF	chr2:152448240-152448390	AG04450	lung:	n/a	n/a
43	CTCF	chr2:152458274-152458761	A549	lung:	n/a	n/a
44	CTCF	chr2:152447828-152448153	Medullo	brain:	n/a	n/a
45	CTCF	chr2:152436283-152436344	Lung_OC	lung:	n/a	n/a
46	CTCF	chr2:152448240-152448390	AG10803	skin:	n/a	n/a
47	CTCF	chr2:152447835-152448140	A549	lung:	n/a	n/a
48	CTCF	chr2:152458330-152458702	A549	lung:	n/a	n/a
49	CTCF	chr2:152437301-152437580	GM13976	blood:	n/a	n/a
50	CTCF	chr2:152458411-152458494	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152440445-152440495	HMEC	breast:	n/a
2	chr2:152440445-152440495	SKMC	muscle:	n/a
3	chr2:152440445-152440495	HUVEC	blood vessel:	n/a
4	chr2:152440445-152440495	SK-N-MC	brain:	n/a
5	chr2:152440445-152440495	IMR90	lung:	fetal
6	chr2:152440445-152440495	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:152440445-152440495	SK-N-SH_RA	brain:	n/a
8	chr2:152440445-152440495	Hepatocyte	liver:	n/a
9	chr2:152440445-152440495	HAEpiC	amniotic membrane:	n/a
10	chr2:152440445-152440495	CMK	blood:	n/a
11	chr2:152440445-152440495	HRPEpiC	eye:	n/a
12	chr2:152440445-152440495	SAEC	small airway:	n/a
13	chr2:152440445-152440495	NHBE	bronchial:	n/a
14	chr2:152440445-152440495	PrEC	prostate:	n/a
15	chr2:152440445-152440495	HCPEpiC	choroid plexus:	n/a
16	chr2:152440445-152440495	LNCaP	prostate:	n/a
17	chr2:152440445-152440495	AG04449	skin:	fetal
18	chr2:152440445-152440495	AG04450	lung:	fetal
19	chr2:152440445-152440495	MCF-7	breast:	n/a
20	chr2:152440445-152440495	GM12891	blood:	n/a
21	chr2:152440445-152440495	NH-A	brain:	n/a
22	chr2:152440445-152440495	AG09319	gingival:	n/a
23	chr2:152440445-152440495	NHDF-neo	bronchial:	n/a
24	chr2:152440445-152440495	NB4	blood:	n/a
25	chr2:152440445-152440495	HCT-116	colon:	n/a
26	chr2:152440445-152440495	H1-hESC	embryonic stem cell:	embryo
27	chr2:152440445-152440495	GM12892	blood:	n/a
28	chr2:152440445-152440495	HNPCEpiC	eye:	n/a
29	chr2:152440445-152440495	RPTEC	kidney:	n/a
30	chr2:152440445-152440495	T-47D	breast:	n/a
31	chr2:152440445-152440495	HL-60	blood:	n/a
32	chr2:152440445-152440495	Jurkat	blood:	n/a
33	chr2:152440445-152440495	SK-N-SH	brain:	n/a
34	chr2:152440445-152440495	HIPEpiC	eye:	n/a
35	chr2:152440445-152440495	HRCEpiC	kidney:	n/a
36	chr2:152440445-152440495	AG10803	skin:	n/a
37	chr2:152440445-152440495	NT2-D1	testis:	n/a
38	chr2:152440445-152440495	U87	brain:	n/a
39	chr2:152440445-152440495	ProgFib	skin:	n/a
40	chr2:152440445-152440495	A549	lung:	n/a
41	chr2:152440445-152440495	PFSK-1	brain:	n/a
42	chr2:152440445-152440495	HCF	heart:	n/a
43	chr2:152440445-152440495	HCM	heart:	n/a
44	chr2:152440445-152440495	ECC-1	luminal epithelium:	n/a
45	chr2:152440445-152440495	Hela-S3	cervix:	n/a
46	chr2:152440445-152440495	PANC-1	pancreas:	n/a
47	chr2:152440445-152440495	GM06990	blood:	n/a
48	chr2:152440445-152440495	MCF10A-Er-Src	breast:	n/a
49	chr2:152440445-152440495	HEEpiC	esophagus:	n/a
50	chr2:152440445-152440495	AG09309	skin:	n/a

No data

Variant related genes	Relation type
NEB	TF binding region
NEB	CpG island

Extended variants
information (count: 258 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62174689	chr2:152435840-152435841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs3815853	chr2:152435852-152435853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542945412	chr2:152435861-152435862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559268680	chr2:152435866-152435867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200703673	chr2:152435886-152435887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113439353	chr2:152435887-152435888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564867595	chr2:152435903-152435904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201111610	chr2:152435919-152435920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370756582	chr2:152435920-152435921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182029307	chr2:152435934-152435935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199521496	chr2:152435960-152435961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62174690	chr2:152436012-152436013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200602229	chr2:152436014-152436015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567524588	chr2:152436101-152436102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536508687	chr2:152436106-152436107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546992311	chr2:152436107-152436108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577964703	chr2:152436274-152436275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201365821	chr2:152436899-152436900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199650389	chr2:152437054-152437055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200658908	chr2:152437135-152437136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573677087	chr2:152437706-152437707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566828890	chr2:152437752-152437753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561161116	chr2:152437753-152437754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531818635	chr2:152437771-152437772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374879543	chr2:152437832-152437833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558993290	chr2:152437956-152437957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575688720	chr2:152437963-152437964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537240072	chr2:152437980-152437981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367881797	chr2:152437986-152437987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573898757	chr2:152437991-152437992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542916866	chr2:152438012-152438013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559417107	chr2:152438057-152438058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572782313	chr2:152438068-152438069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185166179	chr2:152438126-152438127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189923104	chr2:152438147-152438148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530477924	chr2:152438148-152438149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550272381	chr2:152438160-152438161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182498474	chr2:152438180-152438181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565039008	chr2:152438188-152438189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530250693	chr2:152438197-152438198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528116521	chr2:152438206-152438207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188291055	chr2:152438237-152438238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372122164	chr2:152438419-152438420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539013946	chr2:152438469-152438470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552334918	chr2:152438470-152438471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201767726	chr2:152438480-152438481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569276450	chr2:152439687-152439688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538299812	chr2:152439692-152439693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555124282	chr2:152439705-152439706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573859524	chr2:152439737-152439738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	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
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	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
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152409400-152437000	Weak transcription	Psoas Muscle	Psoas
2	chr2:152434000-152466200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr2:152434200-152448200	Weak transcription	HSMMtube	muscle
4	chr2:152434800-152447600	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr2:152434800-152448200	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr2:152435600-152465400	Weak transcription	Fetal Muscle Leg	muscle
7	chr2:152447600-152448800	Strong transcription	Skeletal Muscle Female	skeletal muscle
8	chr2:152448200-152448400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
9	chr2:152448200-152448600	Enhancers	Liver	Liver
10	chr2:152448200-152448800	Strong transcription	HSMMtube	muscle
11	chr2:152448400-152448800	Strong transcription	Skeletal Muscle Male	skeletal muscle
12	chr2:152448800-152460200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr2:152448800-152466000	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr2:152448800-152466200	Weak transcription	HSMMtube	muscle
15	chr2:152460200-152463800	Strong transcription	Skeletal Muscle Female	skeletal muscle
16	chr2:152460600-152489200	Weak transcription	Psoas Muscle	Psoas
17	chr2:152463800-152464000	Genic enhancers	Skeletal Muscle Female	skeletal muscle

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