Variant report

Variant	nsv427886
Chromosome Location	chr11:48850348-49185190
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2724)
CpG islands
(count:2626)
Chromatin interactive
region (count:4)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2724 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48892892-48893269	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:48880376-48880748	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48895975-48896341	HepG2	liver:	n/a	n/a
4	ATF1	chr11:48892890-48893270	K562	blood:	n/a	n/a
5	ATF1	chr11:48940082-48940286	K562	blood:	n/a	n/a
6	ATF1	chr11:48859189-48859770	K562	blood:	n/a	n/a
7	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
8	ATF1	chr11:48883351-48883720	K562	blood:	n/a	n/a
9	ATF1	chr11:48896850-48897050	K562	blood:	n/a	n/a
10	ATF1	chr11:48867583-48867993	K562	blood:	n/a	n/a
11	ATF1	chr11:48880374-48880748	K562	blood:	n/a	n/a
12	ATF3	chr11:48892858-48893151	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:48961635-48962346	K562	blood:	n/a	n/a
14	BACH1	chr11:48881669-48882080	K562	blood:	n/a	n/a
15	BACH1	chr11:48956270-48956471	K562	blood:	n/a	n/a
16	BATF	chr11:48946385-48946719	GM12878	blood:	n/a	n/a
17	BATF	chr11:48943793-48944288	GM12878	blood:	n/a	n/a
18	BATF	chr11:48866749-48866988	GM12878	blood:	n/a	n/a
19	BATF	chr11:48892880-48893156	GM12878	blood:	n/a	n/a
20	BATF	chr11:48934181-48934321	GM12878	blood:	n/a	n/a
21	BATF	chr11:48894524-48895290	GM12878	blood:	n/a	n/a
22	BATF	chr11:48955305-48955628	GM12878	blood:	n/a	n/a
23	BATF	chr11:48985116-48985352	GM12878	blood:	n/a	n/a
24	BATF	chr11:48885554-48885939	GM12878	blood:	n/a	n/a
25	BATF	chr11:48932107-48932317	GM12878	blood:	n/a	n/a
26	BATF	chr11:48877883-48878085	GM12878	blood:	n/a	n/a
27	BATF	chr11:48946780-48947152	GM12878	blood:	n/a	n/a
28	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
29	BATF	chr11:48953227-48953611	GM12878	blood:	n/a	n/a
30	BATF	chr11:48885664-48885889	GM12878	blood:	n/a	n/a
31	BATF	chr11:48976068-48976336	GM12878	blood:	n/a	n/a
32	BATF	chr11:48916722-48917006	GM12878	blood:	n/a	chr11:48916904-48916914
33	BATF	chr11:48854637-48855193	GM12878	blood:	n/a	n/a
34	BATF	chr11:48895950-48896265	GM12878	blood:	n/a	n/a
35	BATF	chr11:48886811-48887099	GM12878	blood:	n/a	n/a
36	BATF	chr11:48883215-48883597	GM12878	blood:	n/a	n/a
37	BATF	chr11:48856704-48856991	GM12878	blood:	n/a	n/a
38	BATF	chr11:48861740-48862096	GM12878	blood:	n/a	n/a
39	BATF	chr11:48877878-48878291	GM12878	blood:	n/a	n/a
40	BATF	chr11:48935181-48935425	GM12878	blood:	n/a	n/a
41	BATF	chr11:48906543-48906879	GM12878	blood:	n/a	chr11:48906618-48906628
42	BATF	chr11:48945011-48945390	GM12878	blood:	n/a	n/a
43	BATF	chr11:48940420-48940720	GM12878	blood:	n/a	n/a
44	BATF	chr11:48887996-48888565	GM12878	blood:	n/a	n/a
45	BATF	chr11:48934428-48934662	GM12878	blood:	n/a	n/a
46	BATF	chr11:48934117-48934343	GM12878	blood:	n/a	n/a
47	BATF	chr11:48895948-48896327	GM12878	blood:	n/a	n/a
48	BATF	chr11:48976038-48976262	GM12878	blood:	n/a	n/a
49	BATF	chr11:48856700-48857102	GM12878	blood:	n/a	n/a
50	BATF	chr11:48931968-48932274	GM12878	blood:	n/a	n/a

(count:2626 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:49124090-49124140	NHDF-neo	bronchial:	n/a
2	chr11:48989769-48989819	MCF-7	breast:	n/a
3	chr11:49072348-49072398	A549	lung:	n/a
4	chr11:49124090-49124140	NHDF-neo	bronchial:	n/a
5	chr11:48989769-48989819	MCF-7	breast:	n/a
6	chr11:49072348-49072398	A549	lung:	n/a
7	chr11:48880009-48880059	NH-A	brain:	n/a
8	chr11:48991619-48991669	NHBE	bronchial:	n/a
9	chr11:49071438-49071488	RPTEC	kidney:	n/a
10	chr11:48990484-48990534	HUVEC	blood vessel:	n/a
11	chr11:48990211-48990261	HRE	kidney:	n/a
12	chr11:49123970-49124020	BJ	skin:	n/a
13	chr11:48987265-48987315	SK-N-MC	brain:	n/a
14	chr11:48880009-48880059	HUVEC	blood vessel:	n/a
15	chr11:49071438-49071488	SK-N-MC	brain:	n/a
16	chr11:48922271-48922321	U87	brain:	n/a
17	chr11:49070231-49070281	GM06990	blood:	n/a
18	chr11:48990211-48990261	HEEpiC	esophagus:	n/a
19	chr11:48901914-48901964	GM12878	blood:	n/a
20	chr11:48923668-48923718	SKMC	muscle:	n/a
21	chr11:48922741-48922791	AoSMC	blood vessel:	n/a
22	chr11:48924804-48924854	GM12892	blood:	n/a
23	chr11:49070637-49070687	SK-N-MC	brain:	n/a
24	chr11:49016314-49016364	NB4	blood:	n/a
25	chr11:48902014-48902064	HCF	heart:	n/a
26	chr11:48923668-48923718	Hepatocyte	liver:	n/a
27	chr11:48990484-48990534	Jurkat	blood:	n/a
28	chr11:48923577-48923627	AG09319	gingival:	n/a
29	chr11:49124111-49124161	HIPEpiC	eye:	n/a
30	chr11:49070637-49070687	HL-60	blood:	n/a
31	chr11:49070231-49070281	GM19239	blood:	n/a
32	chr11:48922674-48922724	NHDF-neo	bronchial:	n/a
33	chr11:49070231-49070281	AG10803	skin:	n/a
34	chr11:49128127-49128177	Hepatocyte	liver:	n/a
35	chr11:49071763-49071813	AG10803	skin:	n/a
36	chr11:49124791-49124841	AG04450	lung:	fetal
37	chr11:48924804-48924854	GM19239	blood:	n/a
38	chr11:49071763-49071813	MCF-7	breast:	n/a
39	chr11:48977834-48977884	GM06990	blood:	n/a
40	chr11:48901705-48901755	HRCEpiC	kidney:	n/a
41	chr11:49124090-49124140	SK-N-MC	brain:	n/a
42	chr11:49071438-49071488	NHBE	bronchial:	n/a
43	chr11:49081540-49081590	HepG2	liver:	n/a
44	chr11:49049039-49049089	GM12891	blood:	n/a
45	chr11:48991619-48991669	CMK	blood:	n/a
46	chr11:48924804-48924854	AG04449	skin:	fetal
47	chr11:48977834-48977884	SAEC	small airway:	n/a
48	chr11:49003361-49003411	K562	blood:	n/a
49	chr11:48994113-48994163	NHBE	bronchial:	n/a
50	chr11:48922269-48922319	T-47D	breast:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:48862246..48863766-chr12:38036979..38038502,2	MCF-7	breast:
2	chr1:121484040..121484766-chr11:48865024..48865526,2	MCF-7	breast:
3	chr1:121484902..121485419-chr11:48946286..48946806,2	MCF-7	breast:
4	chr1:121484496..121485051-chr11:48865024..48865528,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC084851.1-5	chr11:48916513-48916636	NONHSAT021301
2	lnc-AC084851.1-4	chr11:48929840-48930498	NONHSAT021302
3	lnc-AC084851.1-5	chr11:48914808-48914900	NONHSAT021301
4	lnc-AC084851.1-1	chr11:49113956-49114319	NONHSAT021308
5	lnc-TRIM64C-1	chr11:49092304-49092552	NONHSAT021307
6	lnc-AC084851.1-5	chr11:48919540-48919822	NONHSAT021301
7	lnc-AC084851.1-2	chr11:48983254-48983362	NONHSAT021303
8	lnc-AC084851.1-4	chr11:48928655-48928750	NONHSAT021302
9	lnc-AC084851.1-2	chr11:48981480-48981636	NONHSAT021303
10	lnc-AC084851.1-2	chr11:48982485-48982577	NONHSAT021303
11	lnc-AC084851.1-2	chr11:48981775-48981855	NONHSAT021303
12	lnc-AC084851.1-3	chr11:49132308-49132772	NONHSAT021309
13	lnc-AC084851.1-5	chr11:48919940-48920255	NONHSAT021301
14	lnc-FOLH1-1	chr11:49155205-49156352	NONHSAT021310

No data

Variant related genes	Relation type
UBTFL7	TF binding region
ENSG00000205044	TF binding region
TRIM49B	TF binding region
ENSG00000255551	TF binding region
TRIM53CP	TF binding region
ENSG00000254920	TF binding region
ENSG00000254801	TF binding region
ENSG00000254567	TF binding region
FOLH1	TF binding region
ENSG00000254517	TF binding region
ENSG00000255527	TF binding region
TRIM51CP	TF binding region
TRIM51GP	TF binding region
TRIM64C	TF binding region
ENSG00000254412	TF binding region
ENSG00000254993	TF binding region
ENSG00000255452	TF binding region
ENSG00000254728	TF binding region
ENSG00000255338	TF binding region
UBTFL7	CpG island
ENSG00000205044	CpG island
TRIM49B	CpG island
ENSG00000255551	CpG island
TRIM53CP	CpG island
ENSG00000254920	CpG island
ENSG00000254801	CpG island
ENSG00000254567	CpG island
FOLH1	CpG island
ENSG00000254517	CpG island
ENSG00000255527	CpG island
TRIM51CP	CpG island
TRIM51GP	CpG island
TRIM64C	CpG island
ENSG00000254412	CpG island
ENSG00000254993	CpG island
ENSG00000255452	CpG island
ENSG00000254728	CpG island
ENSG00000255338	CpG island

Extended variants
information (count: 11383 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:11383 , 50 per page) page: 1 2 3 4 5 6 7 ... 228

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142916332	chr11:48850349-48850350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139809575	chr11:48850357-48850358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561894734	chr11:48850399-48850400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527678025	chr11:48850411-48850412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547960234	chr11:48850438-48850439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145528065	chr11:48850447-48850448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75058995	chr11:48850450-48850451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113471611	chr11:48850451-48850452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375533555	chr11:48850452-48850453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199524810	chr11:48850464-48850465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143681452	chr11:48850471-48850472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141278488	chr11:48850472-48850473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533578953	chr11:48850483-48850484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550366929	chr11:48850495-48850496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201758935	chr11:48850499-48850500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56391218	chr11:48850587-48850588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570329190	chr11:48850596-48850597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535732317	chr11:48850608-48850609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11040070	chr11:48850623-48850624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565585471	chr11:48850642-48850643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186424853	chr11:48850658-48850659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142896238	chr11:48850664-48850665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550187155	chr11:48850676-48850677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562619894	chr11:48850688-48850689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536869201	chr11:48850712-48850713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556833130	chr11:48850726-48850727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573891084	chr11:48850739-48850740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542599448	chr11:48850773-48850774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56135464	chr11:48850787-48850788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559597796	chr11:48850803-48850804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201708281	chr11:48850808-48850809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200076854	chr11:48850814-48850815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78828690	chr11:48850817-48850818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201580915	chr11:48850818-48850819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs36163696	chr11:48850822-48850823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61898474	chr11:48850841-48850842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199879564	chr11:48850851-48850852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200882542	chr11:48850855-48850856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572380177	chr11:48850865-48850866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201849863	chr11:48850884-48850885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375722225	chr11:48850886-48850887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61898475	chr11:48850887-48850888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61898476	chr11:48850889-48850890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112817018	chr11:48850905-48850906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541399862	chr11:48850908-48850909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564590605	chr11:48850919-48850920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533415737	chr11:48850924-48850925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139822357	chr11:48850946-48850947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs151299319	chr11:48850950-48850951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs118062006	chr11:48850952-48850953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Medulloblastoma	21163964	CNVD
early-passage human iPS cells	21368824	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48848800-48851000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr11:48849600-48853400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr11:48851000-48851600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:48851000-48868000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr11:48851400-48851800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:48851600-48853000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:48851800-48854600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:48852400-48859400	Weak transcription	NHLF	lung
9	chr11:48853000-48853800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr11:48853000-48862600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
11	chr11:48853000-48868800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
12	chr11:48853200-48853600	Weak transcription	K562	blood
13	chr11:48853200-48868800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:48853400-48853800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:48853400-48853800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:48853400-48853800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:48853400-48853800	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
18	chr11:48853400-48853800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
19	chr11:48853400-48854000	ZNF genes & repeats	Fetal Brain Male	brain
20	chr11:48853400-48862800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
21	chr11:48853600-48868200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
22	chr11:48854600-48855000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:48854600-48855400	Weak transcription	Colon Smooth Muscle	Colon
24	chr11:48854600-48855600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
25	chr11:48854600-48855800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
26	chr11:48854800-48855000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
27	chr11:48854800-48855000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
28	chr11:48854800-48855000	Bivalent/Poised TSS	Gastric	stomach
29	chr11:48854800-48855000	ZNF genes & repeats	K562	blood
30	chr11:48855200-48857400	Weak transcription	K562	blood
31	chr11:48855800-48856200	Active TSS	Aorta	Aorta
32	chr11:48855800-48856400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
33	chr11:48856000-48856400	ZNF genes & repeats	Gastric	stomach
34	chr11:48856400-48859200	Weak transcription	Colon Smooth Muscle	Colon
35	chr11:48856400-48859200	Weak transcription	Gastric	stomach
36	chr11:48856800-48857000	ZNF genes & repeats	NH-A	brain
37	chr11:48856800-48857800	ZNF genes & repeats	HUVEC	blood vessel
38	chr11:48857000-48859200	Weak transcription	NH-A	brain
39	chr11:48857400-48859800	ZNF genes & repeats	Adipose Nuclei	Adipose
40	chr11:48857600-48857800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
41	chr11:48858800-48861400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr11:48859000-48859200	Enhancers	HSMMtube	muscle
43	chr11:48859000-48859600	ZNF genes & repeats	HepG2	liver
44	chr11:48859000-48861000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
45	chr11:48859200-48859400	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
46	chr11:48859200-48859400	Bivalent Enhancer	Aorta	Aorta
47	chr11:48859200-48859400	Bivalent/Poised TSS	Psoas Muscle	Psoas
48	chr11:48859200-48859400	Flanking Active TSS	HSMMtube	muscle
49	chr11:48859200-48859600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr11:48859200-48859600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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