Variant report

Variant	nsv897403
Chromosome Location	chr11:48901553-48987539
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:861)
CpG islands
(count:916)
Chromatin interactive
region (count:1)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:861 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:48940082-48940286	K562	blood:	n/a	n/a
2	BACH1	chr11:48961635-48962346	K562	blood:	n/a	n/a
3	BACH1	chr11:48956270-48956471	K562	blood:	n/a	n/a
4	BATF	chr11:48916722-48917006	GM12878	blood:	n/a	chr11:48916904-48916914
5	BATF	chr11:48934117-48934343	GM12878	blood:	n/a	n/a
6	BATF	chr11:48985116-48985352	GM12878	blood:	n/a	n/a
7	BATF	chr11:48976038-48976262	GM12878	blood:	n/a	n/a
8	BATF	chr11:48976068-48976336	GM12878	blood:	n/a	n/a
9	BATF	chr11:48953227-48953611	GM12878	blood:	n/a	n/a
10	BATF	chr11:48934446-48934684	GM12878	blood:	n/a	n/a
11	BATF	chr11:48931968-48932274	GM12878	blood:	n/a	n/a
12	BATF	chr11:48953209-48953631	GM12878	blood:	n/a	n/a
13	BATF	chr11:48955305-48955628	GM12878	blood:	n/a	n/a
14	BATF	chr11:48940420-48940720	GM12878	blood:	n/a	n/a
15	BATF	chr11:48934181-48934321	GM12878	blood:	n/a	n/a
16	BATF	chr11:48946385-48946719	GM12878	blood:	n/a	n/a
17	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
18	BATF	chr11:48945095-48945310	GM12878	blood:	n/a	n/a
19	BATF	chr11:48906543-48906879	GM12878	blood:	n/a	chr11:48906618-48906628
20	BATF	chr11:48935181-48935425	GM12878	blood:	n/a	n/a
21	BATF	chr11:48945011-48945390	GM12878	blood:	n/a	n/a
22	BATF	chr11:48985042-48985405	GM12878	blood:	n/a	n/a
23	BATF	chr11:48946780-48947152	GM12878	blood:	n/a	n/a
24	BATF	chr11:48943793-48944288	GM12878	blood:	n/a	n/a
25	BATF	chr11:48916618-48916954	GM12878	blood:	n/a	chr11:48916904-48916914
26	BATF	chr11:48932107-48932317	GM12878	blood:	n/a	n/a
27	BATF	chr11:48934428-48934662	GM12878	blood:	n/a	n/a
28	BCL11A	chr11:48943783-48944180	GM12878	blood:	n/a	n/a
29	BCL11A	chr11:48932090-48932523	GM12878	blood:	n/a	n/a
30	BCL11A	chr11:48946416-48947156	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:48906540-48906875	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:48916622-48916957	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:48953316-48953636	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:48935779-48936353	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:48945083-48945369	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:48936607-48937112	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:48976050-48976264	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:48953233-48953595	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:48955311-48955544	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:48934158-48934314	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:48934450-48934655	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:48955295-48955655	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:48945083-48945411	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:48932094-48932265	GM12878	blood:	n/a	n/a
45	BHLHE40	chr11:48953193-48953630	HepG2	liver:	n/a	n/a
46	BHLHE40	chr11:48936109-48936382	HepG2	liver:	n/a	n/a
47	BHLHE40	chr11:48948266-48948511	HepG2	liver:	n/a	n/a
48	BHLHE40	chr11:48958418-48958674	HepG2	liver:	n/a	n/a
49	BRCA1	chr11:48942120-48942457	GM12878	blood:	n/a	n/a
50	BRCA1	chr11:48956269-48956471	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48902014-48902064	SK-N-SH	brain:	n/a
2	chr11:48902014-48902064	SK-N-SH	brain:	n/a
3	chr11:48922674-48922724	GM06990	blood:	n/a
4	chr11:48902014-48902064	ECC-1	luminal epithelium:	n/a
5	chr11:48977834-48977884	SKMC	muscle:	n/a
6	chr11:48977527-48977577	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:48923392-48923442	AG09319	gingival:	n/a
8	chr11:48923668-48923718	ovcar-3	ovarian:	n/a
9	chr11:48922741-48922791	H1-hESC	embryonic stem cell:	embryo
10	chr11:48923668-48923718	SK-N-SH	brain:	n/a
11	chr11:48924804-48924854	BE2_C	brain:	n/a
12	chr11:48987265-48987315	Jurkat	blood:	n/a
13	chr11:48923392-48923442	SAEC	small airway:	n/a
14	chr11:48901705-48901755	Caco-2	colon:	n/a
15	chr11:48923577-48923627	AG10803	skin:	n/a
16	chr11:48923392-48923442	BE2_C	brain:	n/a
17	chr11:48922269-48922319	NB4	blood:	n/a
18	chr11:48923668-48923718	U87	brain:	n/a
19	chr11:48923392-48923442	AG09309	skin:	n/a
20	chr11:48923668-48923718	BJ	skin:	n/a
21	chr11:48977527-48977577	GM19239	blood:	n/a
22	chr11:48923392-48923442	LNCaP	prostate:	n/a
23	chr11:48902014-48902064	H1-hESC	embryonic stem cell:	embryo
24	chr11:48923668-48923718	NH-A	brain:	n/a
25	chr11:48922674-48922724	ECC-1	luminal epithelium:	n/a
26	chr11:48923392-48923442	MCF-7	breast:	n/a
27	chr11:48923392-48923442	SK-N-SH_RA	brain:	n/a
28	chr11:48922269-48922319	AG10803	skin:	n/a
29	chr11:48923392-48923442	Caco-2	colon:	n/a
30	chr11:48901914-48901964	ECC-1	luminal epithelium:	n/a
31	chr11:48922271-48922321	HIPEpiC	eye:	n/a
32	chr11:48977834-48977884	HMEC	breast:	n/a
33	chr11:48977527-48977577	HUVEC	blood vessel:	n/a
34	chr11:48901914-48901964	AG09319	gingival:	n/a
35	chr11:48923668-48923718	SAEC	small airway:	n/a
36	chr11:48922741-48922791	Hela-S3	cervix:	n/a
37	chr11:48922269-48922319	MCF-7	breast:	n/a
38	chr11:48987265-48987315	AG09309	skin:	n/a
39	chr11:48901914-48901964	NHBE	bronchial:	n/a
40	chr11:48901705-48901755	BJ	skin:	n/a
41	chr11:48987265-48987315	HUVEC	blood vessel:	n/a
42	chr11:48922035-48922085	SK-N-SH_RA	brain:	n/a
43	chr11:48922271-48922321	SK-N-SH	brain:	n/a
44	chr11:48922271-48922321	Hela-S3	cervix:	n/a
45	chr11:48923392-48923442	MCF10A-Er-Src	breast:	n/a
46	chr11:48987265-48987315	AG04449	skin:	fetal
47	chr11:48923577-48923627	SK-N-SH_RA	brain:	n/a
48	chr11:48922741-48922791	PFSK-1	brain:	n/a
49	chr11:48922741-48922791	HCPEpiC	choroid plexus:	n/a
50	chr11:48923668-48923718	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:121484902..121485419-chr11:48946286..48946806,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC084851.1-4	chr11:48928655-48928750	NONHSAT021302
2	lnc-AC084851.1-5	chr11:48919940-48920255	NONHSAT021301
3	lnc-AC084851.1-2	chr11:48983254-48983362	NONHSAT021303
4	lnc-AC084851.1-5	chr11:48919540-48919822	NONHSAT021301
5	lnc-AC084851.1-4	chr11:48929840-48930498	NONHSAT021302
6	lnc-AC084851.1-2	chr11:48981480-48981636	NONHSAT021303
7	lnc-AC084851.1-5	chr11:48916513-48916636	NONHSAT021301
8	lnc-AC084851.1-2	chr11:48982485-48982577	NONHSAT021303
9	lnc-AC084851.1-5	chr11:48914808-48914900	NONHSAT021301
10	lnc-AC084851.1-2	chr11:48981775-48981855	NONHSAT021303

No data

Variant related genes	Relation type
ENSG00000255551	TF binding region
ENSG00000254920	TF binding region
ENSG00000254517	TF binding region
ENSG00000255527	TF binding region
TRIM51CP	TF binding region
ENSG00000254728	TF binding region
ENSG00000255551	CpG island
ENSG00000254920	CpG island
ENSG00000254517	CpG island
ENSG00000255527	CpG island
TRIM51CP	CpG island
ENSG00000254728	CpG island

Extended variants
information (count: 4516 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:4516 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570921895	chr11:48901637-48901638	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs114786920	chr11:48901640-48901641	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs185495613	chr11:48901651-48901652	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs570383685	chr11:48901656-48901657	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs190449516	chr11:48901669-48901670	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs556077902	chr11:48901692-48901693	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs371510893	chr11:48901702-48901703	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs534606123	chr11:48901715-48901716	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs557573875	chr11:48901724-48901725	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs532395641	chr11:48901725-48901726	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs113263077	chr11:48901727-48901728	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs375097209	chr11:48901728-48901729	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs556711176	chr11:48901732-48901733	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs149931229	chr11:48901734-48901735	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs181690644	chr11:48901735-48901736	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs374937498	chr11:48901742-48901743	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs559214108	chr11:48901744-48901745	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs368438190	chr11:48901745-48901746	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs144944254	chr11:48901763-48901764	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs541374463	chr11:48901780-48901781	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs56132995	chr11:48901799-48901800	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs549984939	chr11:48901811-48901812	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs111900241	chr11:48901818-48901819	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs529497783	chr11:48901828-48901829	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs115591810	chr11:48901849-48901850	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs564232435	chr11:48901854-48901855	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs111549660	chr11:48901858-48901859	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs1967411	chr11:48901867-48901868	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551323699	chr11:48901875-48901876	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs547841214	chr11:48901876-48901877	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs187100155	chr11:48901888-48901889	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs537180903	chr11:48901896-48901897	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs556623062	chr11:48901897-48901898	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs573541170	chr11:48901898-48901899	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs568057585	chr11:48901909-48901910	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs116166527	chr11:48901921-48901922	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs192452620	chr11:48901932-48901933	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs541087145	chr11:48901940-48901941	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs564531943	chr11:48901945-48901946	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs577942017	chr11:48901951-48901952	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs543971375	chr11:48901952-48901953	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs76428160	chr11:48901956-48901957	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs183954490	chr11:48901963-48901964	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs549560196	chr11:48901975-48901976	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs146657934	chr11:48901976-48901977	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs528758489	chr11:48901980-48901981	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs551768863	chr11:48901995-48901996	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs571256548	chr11:48901999-48902000	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs369204932	chr11:48902000-48902001	Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs532079666	chr11:48910217-48910218	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48901600-48902000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr11:48901600-48902000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:48901600-48902000	ZNF genes & repeats	Esophagus	oesophagus
4	chr11:48901800-48902000	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:48901800-48902000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:48921600-48922600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:48930400-48935800	Weak transcription	K562	blood
8	chr11:48931400-48933600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr11:48932200-48934000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr11:48932400-48932800	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
11	chr11:48932400-48932800	Active TSS	Aorta	Aorta
12	chr11:48932400-48933000	ZNF genes & repeats	Liver	Liver
13	chr11:48932600-48932800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
14	chr11:48932600-48932800	ZNF genes & repeats	HUVEC	blood vessel
15	chr11:48932600-48933000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:48932800-48933200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:48932800-48936200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr11:48933200-48935400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:48934200-48939800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:48935200-48947600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
21	chr11:48935400-48935800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:48935600-48936400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
23	chr11:48935600-48943800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:48935800-48936400	ZNF genes & repeats	K562	blood
25	chr11:48935800-48942400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
26	chr11:48936000-48936600	ZNF genes & repeats	HUVEC	blood vessel
27	chr11:48936000-48936600	ZNF genes & repeats	NH-A	brain
28	chr11:48936200-48936600	ZNF genes & repeats	HMEC	breast
29	chr11:48936400-48949200	Weak transcription	K562	blood
30	chr11:48936600-48940600	Weak transcription	NH-A	brain
31	chr11:48937400-48939000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
32	chr11:48938000-48949200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr11:48938200-48938400	ZNF genes & repeats	Left Ventricle	heart
34	chr11:48938200-48938400	ZNF genes & repeats	HUVEC	blood vessel
35	chr11:48938400-48939400	Weak transcription	HUVEC	blood vessel
36	chr11:48939400-48939800	ZNF genes & repeats	HUVEC	blood vessel
37	chr11:48940000-48940400	Active TSS	Small Intestine	intestine
38	chr11:48943200-48944000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
39	chr11:48947600-48948400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr11:48947600-48948400	ZNF genes & repeats	HUVEC	blood vessel
41	chr11:48949000-48949200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr11:48953000-48954400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:48953000-48959800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
44	chr11:48953200-48959800	Weak transcription	K562	blood
45	chr11:48955000-48959000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
46	chr11:48955200-48955600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:48956200-48963400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
48	chr11:48956600-48964400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:48957400-48958800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:48957800-48958400	ZNF genes & repeats	HUVEC	blood vessel

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