Variant report

Variant	nsv7732
Chromosome Location	chr11:33429512-33474692
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	chr11:33467294-33467606	HepG2	liver:	n/a	n/a
2	CEBPB	chr11:33468747-33468988	IMR90	lung:	n/a	chr11:33468877-33468890 chr11:33468878-33468889
3	CEBPB	chr11:33468723-33468936	A549	lung:	n/a	chr11:33468877-33468890 chr11:33468878-33468889
4	CEBPB	chr11:33474376-33474661	IMR90	lung:	n/a	n/a
5	CEBPB	chr11:33468792-33469028	HepG2	liver:	n/a	chr11:33468877-33468890 chr11:33468878-33468889
6	CTCF	chr11:33474585-33474598	IMR90	lung:	n/a	n/a
7	CTCF	chr11:33467180-33467330	HPAF	blood vessel:	n/a	n/a
8	CTCF	chr11:33474560-33474710	AG09319	gingival:	n/a	n/a
9	CTCF	chr11:33467200-33467350	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr11:33474580-33474730	AG04449	skin:	n/a	n/a
11	CTCF	chr11:33459220-33459370	Caco-2	colon:	n/a	n/a
12	CTCF	chr11:33474620-33474770	BJ	skin:	n/a	n/a
13	CTCF	chr11:33474620-33474770	HMF	breast:	n/a	n/a
14	CTCF	chr11:33467120-33467270	HepG2	liver:	n/a	n/a
15	CTCF	chr11:33453043-33453114	GM10248	blood:	n/a	n/a
16	CTCF	chr11:33474500-33474650	BJ	skin:	n/a	n/a
17	CTCF	chr11:33474580-33474730	AG04450	lung:	n/a	n/a
18	CTCF	chr11:33474540-33474690	HMF	breast:	n/a	n/a
19	CTCF	chr11:33467200-33467350	HMF	breast:	n/a	n/a
20	CTCF	chr11:33467200-33467350	AG09319	gingival:	n/a	n/a
21	CTCF	chr11:33474655-33474687	ProgFib	skin:	n/a	n/a
22	CTCF	chr11:33467140-33467290	HMF	breast:	n/a	n/a
23	CTCF	chr11:33474580-33474730	AG09319	gingival:	n/a	n/a
24	CTCF	chr11:33432289-33432309	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr11:33437000-33437150	GM12873	blood:	n/a	n/a
26	E2F4	chr11:33470401-33470601	MCF10A-Er-Src	breast:	n/a	n/a
27	EP300	chr11:33466756-33467250	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr11:33466279-33467758	SK-N-SH	brain:	n/a	chr11:33466547-33466556
29	EP300	chr11:33471176-33471947	SK-N-SH	brain:	n/a	n/a
30	EP300	chr11:33474319-33474722	SK-N-SH_RA	brain:	n/a	chr11:33474486-33474499
31	EP300	chr11:33474300-33474722	SK-N-SH_RA	brain:	n/a	chr11:33474486-33474499
32	EP300	chr11:33465849-33467801	SK-N-SH	brain:	n/a	chr11:33466547-33466556
33	EP300	chr11:33466618-33467771	SK-N-SH	brain:	n/a	n/a
34	EP300	chr11:33474151-33474880	SK-N-SH	brain:	n/a	chr11:33474486-33474499
35	EP300	chr11:33466751-33467228	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr11:33472971-33473287	SK-N-SH_RA	brain:	n/a	chr11:33472994-33473004 chr11:33473132-33473142
37	EP300	chr11:33473044-33473261	SK-N-SH_RA	brain:	n/a	chr11:33473132-33473142
38	FOS	chr11:33474264-33474751	HUVEC	blood vessel:	n/a	chr11:33474511-33474519 chr11:33474510-33474520 chr11:33474533-33474544 chr11:33474509-33474520 chr11:33474510-33474520 chr11:33474535-33474542 chr11:33474530-33474541 chr11:33474632-33474644 chr11:33474510-33474520 chr11:33474510-33474520
39	FOS	chr11:33474330-33474975	MCF10A-Er-Src	breast:	n/a	chr11:33474511-33474519 chr11:33474510-33474520 chr11:33474533-33474544 chr11:33474509-33474520 chr11:33474510-33474520 chr11:33474535-33474542 chr11:33474530-33474541 chr11:33474632-33474644 chr11:33474510-33474520 chr11:33474510-33474520
40	FOS	chr11:33466426-33466686	MCF10A-Er-Src	breast:	n/a	chr11:33466547-33466557 chr11:33466544-33466555 chr11:33466547-33466557 chr11:33466547-33466557 chr11:33466546-33466557 chr11:33466548-33466557 chr11:33466547-33466557
41	FOS	chr11:33474344-33474692	MCF10A-Er-Src	breast:	n/a	chr11:33474511-33474519 chr11:33474510-33474520 chr11:33474533-33474544 chr11:33474509-33474520 chr11:33474510-33474520 chr11:33474535-33474542 chr11:33474530-33474541 chr11:33474632-33474644 chr11:33474510-33474520 chr11:33474510-33474520
42	FOS	chr11:33466394-33466686	MCF10A-Er-Src	breast:	n/a	chr11:33466547-33466557 chr11:33466544-33466555 chr11:33466547-33466557 chr11:33466547-33466557 chr11:33466546-33466557 chr11:33466548-33466557 chr11:33466547-33466557
43	FOS	chr11:33468837-33468945	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr11:33470172-33470680	HUVEC	blood vessel:	n/a	chr11:33470488-33470499 chr11:33470465-33470475 chr11:33470464-33470475 chr11:33470465-33470475 chr11:33470465-33470475
45	FOS	chr11:33466390-33467020	HUVEC	blood vessel:	n/a	chr11:33466547-33466557 chr11:33466544-33466555 chr11:33466547-33466557 chr11:33466547-33466557 chr11:33466546-33466557 chr11:33466548-33466557 chr11:33466547-33466557
46	FOS	chr11:33470321-33470609	MCF10A-Er-Src	breast:	n/a	chr11:33470488-33470499 chr11:33470465-33470475 chr11:33470464-33470475 chr11:33470465-33470475 chr11:33470465-33470475
47	FOS	chr11:33470289-33470710	MCF10A-Er-Src	breast:	n/a	chr11:33470488-33470499 chr11:33470465-33470475 chr11:33470464-33470475 chr11:33470465-33470475 chr11:33470465-33470475
48	FOS	chr11:33470311-33470607	MCF10A-Er-Src	breast:	n/a	chr11:33470488-33470499 chr11:33470465-33470475 chr11:33470464-33470475 chr11:33470465-33470475 chr11:33470465-33470475
49	FOS	chr11:33473255-33473299	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr11:33474332-33474708	MCF10A-Er-Src	breast:	n/a	chr11:33474511-33474519 chr11:33474510-33474520 chr11:33474533-33474544 chr11:33474509-33474520 chr11:33474510-33474520 chr11:33474535-33474542 chr11:33474530-33474541 chr11:33474632-33474644 chr11:33474510-33474520 chr11:33474510-33474520

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33442321-33442371	HCT-116	colon:	n/a
2	chr11:33442321-33442371	H1-hESC	embryonic stem cell:	embryo
3	chr11:33453389-33453439	HRCEpiC	kidney:	n/a
4	chr11:33453389-33453439	LNCaP	prostate:	n/a
5	chr11:33453389-33453439	NT2-D1	testis:	n/a
6	chr11:33474484-33474534	LNCaP	prostate:	n/a
7	chr11:33442321-33442371	CMK	blood:	n/a
8	chr11:33474484-33474534	AG04449	skin:	fetal
9	chr11:33474484-33474534	GM12892	blood:	n/a
10	chr11:33453389-33453439	HCT-116	colon:	n/a
11	chr11:33442321-33442371	AG10803	skin:	n/a
12	chr11:33474484-33474534	NHDF-neo	bronchial:	n/a
13	chr11:33442321-33442371	HEEpiC	esophagus:	n/a
14	chr11:33453389-33453439	HRE	kidney:	n/a
15	chr11:33442321-33442371	HL-60	blood:	n/a
16	chr11:33474484-33474534	ovcar-3	ovarian:	n/a
17	chr11:33442321-33442371	NHDF-neo	bronchial:	n/a
18	chr11:33442321-33442371	HRCEpiC	kidney:	n/a
19	chr11:33453389-33453439	NH-A	brain:	n/a
20	chr11:33453389-33453439	A549	lung:	n/a
21	chr11:33453389-33453439	AG10803	skin:	n/a
22	chr11:33474484-33474534	AG09319	gingival:	n/a
23	chr11:33474484-33474534	SK-N-MC	brain:	n/a
24	chr11:33474484-33474534	HCT-116	colon:	n/a
25	chr11:33474484-33474534	CMK	blood:	n/a
26	chr11:33474484-33474534	U87	brain:	n/a
27	chr11:33442321-33442371	HepG2	liver:	n/a
28	chr11:33442321-33442371	T-47D	breast:	n/a
29	chr11:33453389-33453439	SKMC	muscle:	n/a
30	chr11:33442321-33442371	SAEC	small airway:	n/a
31	chr11:33442321-33442371	ovcar-3	ovarian:	n/a
32	chr11:33453389-33453439	AG04450	lung:	fetal
33	chr11:33442321-33442371	AoSMC	blood vessel:	n/a
34	chr11:33474484-33474534	A549	lung:	n/a
35	chr11:33453389-33453439	Hela-S3	cervix:	n/a
36	chr11:33453389-33453439	NHBE	bronchial:	n/a
37	chr11:33442321-33442371	GM12891	blood:	n/a
38	chr11:33474484-33474534	HEK293	kidney:	embryo
39	chr11:33453389-33453439	HMEC	breast:	n/a
40	chr11:33453389-33453439	H1-hESC	embryonic stem cell:	embryo
41	chr11:33474484-33474534	Hela-S3	cervix:	n/a
42	chr11:33474484-33474534	SK-N-SH	brain:	n/a
43	chr11:33453389-33453439	MCF-7	breast:	n/a
44	chr11:33442321-33442371	MCF-7	breast:	n/a
45	chr11:33442321-33442371	HCPEpiC	choroid plexus:	n/a
46	chr11:33474484-33474534	GM19239	blood:	n/a
47	chr11:33453389-33453439	HIPEpiC	eye:	n/a
48	chr11:33474484-33474534	Caco-2	colon:	n/a
49	chr11:33453389-33453439	GM12891	blood:	n/a
50	chr11:33442321-33442371	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
2	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
3	chr11:33432981..33435559-chr11:33436354..33439310,2	K562	blood:
4	chr11:33426996..33428983-chr11:33431666..33434178,3	K562	blood:
5	chr11:33432981..33435559-chr11:33436354..33439310,2	K562	blood:
6	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
7	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
8	chr11:33428202..33430119-chr11:33432481..33434506,2	MCF-7	breast:
9	chr11:33422636..33425023-chr11:33427111..33429775,2	MCF-7	breast:
10	chr11:33428202..33430119-chr11:33432481..33434506,2	MCF-7	breast:
11	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
12	chr11:33450480..33453431-chr11:33470843..33473158,2	MCF-7	breast:
13	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
14	chr11:33421417..33423758-chr11:33435787..33437817,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf41-5	chr11:33472192-33472489	NONHSAT018701

Variant related genes	Relation type
ENSG00000255207	TF binding region
ENSG00000255207	CpG island
ENSG00000255207	chromatin interactions
ENSG00000254537	chromatin interactions

Extended variants
information (count: 1735 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1735 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368934845	chr11:33429579-33429580	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs4755589	chr11:33429598-33429599	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534853845	chr11:33429636-33429637	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs190669520	chr11:33429637-33429638	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147716601	chr11:33429664-33429665	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543764587	chr11:33429706-33429707	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563465704	chr11:33429801-33429802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532220114	chr11:33429810-33429811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182527125	chr11:33429811-33429812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566085760	chr11:33429817-33429818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528456146	chr11:33429818-33429819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368036868	chr11:33429885-33429886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550123175	chr11:33429903-33429904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187112131	chr11:33429906-33429907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200757801	chr11:33429909-33429910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568391192	chr11:33429925-33429926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189655878	chr11:33429989-33429990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141068418	chr11:33429990-33429991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141299631	chr11:33430007-33430008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552986914	chr11:33430009-33430010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551963001	chr11:33430031-33430032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138063173	chr11:33430035-33430036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34208718	chr11:33430036-33430037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4756678	chr11:33430037-33430038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200262359	chr11:33430039-33430040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150511957	chr11:33430056-33430057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58439063	chr11:33430057-33430058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35886017	chr11:33430061-33430062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188949896	chr11:33430125-33430126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566460718	chr11:33430143-33430144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558611012	chr11:33430144-33430145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370983709	chr11:33430226-33430227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572206330	chr11:33430241-33430242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs71480909	chr11:33430253-33430254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544645908	chr11:33430273-33430274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370014889	chr11:33430325-33430326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12286069	chr11:33430326-33430327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537601705	chr11:33430328-33430329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541006521	chr11:33430353-33430354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554577671	chr11:33430364-33430365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574503309	chr11:33430380-33430381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12272969	chr11:33430383-33430384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113295850	chr11:33430386-33430387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150259527	chr11:33430396-33430397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193106095	chr11:33430442-33430443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547873161	chr11:33430450-33430451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373691087	chr11:33430483-33430484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs60590374	chr11:33430484-33430485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs559404287	chr11:33430485-33430486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374096925	chr11:33430496-33430497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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	18451855	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33413400-33466200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:33415600-33434000	Weak transcription	Fetal Brain Female	brain
3	chr11:33423800-33433000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:33423800-33433400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:33423800-33434000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr11:33424000-33432400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:33424000-33440200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:33428200-33431400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr11:33428400-33432000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:33429200-33429800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:33429600-33433600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr11:33430800-33432000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr11:33431400-33432000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:33431400-33433600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr11:33431600-33433600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr11:33431800-33432600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:33431800-33432600	Enhancers	HSMM	muscle
18	chr11:33431800-33433000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr11:33431800-33433400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:33432000-33432800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr11:33432000-33433000	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr11:33432000-33433400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:33432400-33433000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:33432600-33444000	Weak transcription	HSMM	muscle
25	chr11:33432800-33433200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr11:33433000-33433600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr11:33433000-33435000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr11:33433200-33433400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:33433200-33433600	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr11:33433200-33434200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:33433400-33434200	Enhancers	Brain Cingulate Gyrus	brain
32	chr11:33433400-33434800	Enhancers	GM12878-XiMat	blood
33	chr11:33433400-33435000	Enhancers	HSMMtube	muscle
34	chr11:33433400-33435400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr11:33433400-33435800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr11:33433400-33442800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:33433600-33434600	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr11:33433800-33434200	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr11:33433800-33434400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:33433800-33434600	Enhancers	Osteobl	bone
41	chr11:33434000-33434200	Enhancers	Fetal Brain Female	brain
42	chr11:33434000-33434400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr11:33434000-33434400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr11:33434000-33434600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:33434000-33434800	Enhancers	NH-A	brain
46	chr11:33434000-33435600	Enhancers	NHDF-Ad	bronchial
47	chr11:33434600-33435000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr11:33435000-33435400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr11:33435000-33440000	Weak transcription	HSMMtube	muscle
50	chr11:33435000-33443600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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