Variant report

Variant	esv1851630
Chromosome Location	chr11:32972567-32986329
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:32975953-32975956	K562	blood:	n/a	n/a
2	BHLHE40	chr11:32982189-32982478	GM12878	blood:	n/a	n/a
3	CEBPB	chr11:32982015-32982083	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr11:32982220-32982370	HPF	lung:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
5	CTCF	chr11:32982193-32982417	LNCaP	prostate:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
6	CTCF	chr11:32982240-32982390	HEK293	kidney:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
7	CTCF	chr11:32982220-32982370	BE2_C	brain:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
8	CTCF	chr11:32982220-32982370	HBMEC	blood vessel:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
9	CTCF	chr11:32982220-32982370	HCFaa	heart:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
10	CTCF	chr11:32982220-32982370	BJ	skin:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
11	CTCF	chr11:32982000-32982150	NHEK	skin:	n/a	n/a
12	CTCF	chr11:32982240-32982390	SK-N-SH_RA	brain:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
13	CTCF	chr11:32982200-32982350	HUVEC	blood vessel:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
14	CTCF	chr11:32982201-32982429	GM12878	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
15	CTCF	chr11:32982220-32982370	GM12872	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
16	CTCF	chr11:32982240-32982390	RPTEC	kidney:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
17	CTCF	chr11:32981656-32981709	Fibrobl	skin:	n/a	n/a
18	CTCF	chr11:32982018-32982762	SK-N-SH	brain:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
19	CTCF	chr11:32982092-32982607	HCT-116	colon:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
20	CTCF	chr11:32982253-32982351	GM13976	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
21	CTCF	chr11:32982220-32982370	HMF	breast:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
22	CTCF	chr11:32982200-32982350	HBMEC	blood vessel:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
23	CTCF	chr11:32982240-32982390	HPAF	blood vessel:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
24	CTCF	chr11:32981389-32981400	A549	lung:	n/a	n/a
25	CTCF	chr11:32982180-32982330	GM12868	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
26	CTCF	chr11:32982208-32982412	GM10248	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
27	CTCF	chr11:32982220-32982370	K562	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
28	CTCF	chr11:32982193-32982426	Kidney_OC	kidney:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
29	CTCF	chr11:32982260-32982410	HAc	cerebellar:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
30	CTCF	chr11:32982221-32982399	A549	lung:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
31	CTCF	chr11:32982240-32982390	AG09319	gingival:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
32	CTCF	chr11:32982240-32982390	AG04449	skin:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
33	CTCF	chr11:32982040-32982190	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr11:32982220-32982370	GM12873	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
35	CTCF	chr11:32982240-32982390	GM12872	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
36	CTCF	chr11:32982200-32982350	SAEC	small airway:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
37	CTCF	chr11:32982260-32982410	GM06990	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
38	CTCF	chr11:32982200-32982350	Hela-S3	cervix:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
39	CTCF	chr11:32982180-32982330	GM12878	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
40	CTCF	chr11:32982166-32982453	HUVEC	blood vessel:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
41	CTCF	chr11:32982100-32982250	HCM	heart:	n/a	n/a
42	CTCF	chr11:32982240-32982390	HCT-116	colon:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
43	CTCF	chr11:32982103-32982532	GM12878	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
44	CTCF	chr11:32982220-32982370	HEEpiC	esophagus:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
45	CTCF	chr11:32982220-32982370	AG09319	gingival:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
46	CTCF	chr11:32982180-32982330	GM12867	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
47	CTCF	chr11:32982040-32982190	HAc	cerebellar:	n/a	n/a
48	CTCF	chr11:32982180-32982330	GM12864	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
49	CTCF	chr11:32982210-32982437	A549	lung:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318
50	CTCF	chr11:32982240-32982390	HL-60	blood:	n/a	chr11:32982307-32982325 chr11:32982308-32982324 chr11:32982309-32982330 chr11:32982311-32982318

No.	Distal block	Cell Line	Cell type
1	chr11:32982353..32983263-chr11:33086839..33087416,2	MCF-7	breast:
2	chr11:32970671..32972775-chr11:32979842..32982658,2	K562	blood:
3	chr11:32982056..32982733-chr11:33350989..33351739,2	K562	blood:
4	chr11:32915892..32917470-chr11:32980726..32982282,2	K562	blood:
5	chr11:32982327..32984023-chr11:33390393..33392493,2	K562	blood:
6	chr11:32914058..32916371-chr11:32975765..32977557,2	MCF-7	breast:
7	chr11:32982069..32982796-chr11:33086887..33087818,6	K562	blood:
8	chr11:32981687..32982746-chr11:33086877..33087798,8	MCF-7	breast:
9	chr11:32970671..32972775-chr11:32979842..32982658,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSTF3-1	chr11:32978271-32978312	NONHSAT018681
2	lnc-CSTF3-1	chr11:32977870-32978000	NONHSAT018681

Variant related genes	Relation type
QSER1	TF binding region
ENSG00000060749	chromatin interactions

Extended variants
information (count: 422 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7395350	chr11:32972567-32972568	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537147918	chr11:32972570-32972571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534089308	chr11:32972572-32972573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141334152	chr11:32972703-32972704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184067893	chr11:32972772-32972773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536375152	chr11:32972788-32972789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556260618	chr11:32972830-32972831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555773992	chr11:32972853-32972854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs55852973	chr11:32972886-32972887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187241292	chr11:32972889-32972890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567564113	chr11:32972951-32972952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79821042	chr11:32973089-32973090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143587612	chr11:32973090-32973091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572697645	chr11:32973108-32973109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534986655	chr11:32973140-32973141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541702340	chr11:32973221-32973222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs151013722	chr11:32973284-32973285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192545292	chr11:32973326-32973327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542618616	chr11:32973373-32973374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184350114	chr11:32973374-32973375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34354021	chr11:32973384-32973385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113407514	chr11:32973385-32973386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397703245	chr11:32973400-32973401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189637102	chr11:32973469-32973470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551331363	chr11:32973470-32973471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565079000	chr11:32973471-32973472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527621706	chr11:32973477-32973478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547268452	chr11:32973605-32973606	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116876723	chr11:32973678-32973679	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545644154	chr11:32973737-32973738	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536260863	chr11:32973787-32973788	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182051459	chr11:32973792-32973793	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570056610	chr11:32973831-32973832	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539122096	chr11:32973833-32973834	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184818694	chr11:32973836-32973837	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188848166	chr11:32973921-32973922	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535370157	chr11:32973930-32973931	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79097646	chr11:32973946-32973947	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397823615	chr11:32973947-32973948	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs397831412	chr11:32973949-32973950	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555326623	chr11:32973999-32974000	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142119610	chr11:32974013-32974014	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575153812	chr11:32974014-32974015	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76612822	chr11:32974015-32974016	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542655578	chr11:32974039-32974040	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556118402	chr11:32974083-32974084	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542366333	chr11:32974219-32974220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537332686	chr11:32974294-32974295	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368440623	chr11:32974349-32974350	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540825544	chr11:32974350-32974351	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32950400-32994400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr11:32953800-32978400	Weak transcription	Fetal Intestine Small	intestine
3	chr11:32954600-32990200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:32955400-32994200	Weak transcription	Gastric	stomach
5	chr11:32955400-32994400	Weak transcription	Esophagus	oesophagus
6	chr11:32955600-32987200	Weak transcription	Right Ventricle	heart
7	chr11:32955600-33000800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr11:32955600-33003800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr11:32956000-32975400	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr11:32956200-32979400	Weak transcription	Colon Smooth Muscle	Colon
11	chr11:32956200-32994200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:32956800-32975400	Weak transcription	Lung	lung
13	chr11:32956800-32975400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr11:32956800-32975400	Weak transcription	NHEK	skin
15	chr11:32956800-32977800	Weak transcription	Left Ventricle	heart
16	chr11:32956800-32977800	Weak transcription	Thymus	Thymus
17	chr11:32956800-32994200	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr11:32957000-32978400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr11:32957000-32978400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr11:32957200-32978800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr11:32957200-32979200	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr11:32957400-32975400	Weak transcription	Fetal Brain Male	brain
23	chr11:32957400-32975400	Weak transcription	HMEC	breast
24	chr11:32957400-32976400	Weak transcription	NHDF-Ad	bronchial
25	chr11:32957600-32978400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr11:32958000-32979600	Weak transcription	Fetal Kidney	kidney
27	chr11:32958400-32975400	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr11:32958600-32975200	Weak transcription	A549	lung
29	chr11:32958600-32980600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr11:32958800-32977800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr11:32958800-32978600	Weak transcription	NH-A	brain
32	chr11:32959200-32977800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr11:32959200-32977800	Weak transcription	Fetal Muscle Leg	muscle
34	chr11:32959200-32978000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:32959400-32975400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr11:32959600-32978400	Weak transcription	Brain Germinal Matrix	brain
37	chr11:32960000-32974600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr11:32960000-32975400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr11:32960200-32975400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:32960200-32975400	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr11:32960200-32975400	Weak transcription	Primary T cells from cord blood	blood
42	chr11:32960200-32975400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr11:32960200-32975400	Weak transcription	HepG2	liver
44	chr11:32960200-32975400	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr11:32960200-32978400	Weak transcription	K562	blood
46	chr11:32960200-32979600	Weak transcription	Fetal Brain Female	brain
47	chr11:32961800-32975400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr11:32962400-32994400	Weak transcription	Fetal Heart	heart
49	chr11:32962600-32975200	Weak transcription	Dnd41	blood
50	chr11:32963200-32973800	Weak transcription	H1 Cell Line	embryonic stem cell

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