Variant report

Variant	nsv933979
Chromosome Location	chr11:67374045-67374409
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:634)
CpG islands
(count:244)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:67374041-67374553	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:67374108-67374566	K562	blood:	n/a	n/a
3	ATF1	chr11:67374081-67374597	K562	blood:	n/a	n/a
4	ATF2	chr11:67374266-67374561	GM12878	blood:	n/a	n/a
5	ATF2	chr11:67374118-67374518	GM12878	blood:	n/a	n/a
6	ATF3	chr11:67374149-67374594	H1-hESC	embryonic stem cell:	n/a	chr11:67374348-67374368 chr11:67374373-67374393 chr11:67374373-67374384
7	ATF3	chr11:67373993-67374574	K562	blood:	n/a	chr11:67374348-67374368 chr11:67374373-67374393 chr11:67374373-67374384
8	ATF3	chr11:67374144-67374589	H1-hESC	embryonic stem cell:	n/a	chr11:67374348-67374368 chr11:67374373-67374393 chr11:67374373-67374384
9	ATF3	chr11:67374155-67374502	HepG2	liver:	n/a	chr11:67374348-67374368 chr11:67374373-67374393 chr11:67374373-67374384
10	ATF3	chr11:67374172-67374550	A549	lung:	n/a	chr11:67374348-67374368 chr11:67374373-67374393 chr11:67374373-67374384
11	ATF3	chr11:67373996-67374565	GM12878	blood:	n/a	chr11:67374348-67374368 chr11:67374373-67374393 chr11:67374373-67374384
12	ATF3	chr11:67374217-67374574	K562	blood:	n/a	chr11:67374348-67374368 chr11:67374373-67374393 chr11:67374373-67374384
13	ATF3	chr11:67374237-67374463	GM12878	blood:	n/a	chr11:67374348-67374368 chr11:67374373-67374393 chr11:67374373-67374384
14	BACH1	chr11:67374266-67374563	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCLAF1	chr11:67374001-67374627	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:67372856-67374573	K562	blood:	n/a	n/a
17	BHLHE40	chr11:67374196-67374535	HepG2	liver:	n/a	n/a
18	BHLHE40	chr11:67374146-67374583	GM12878	blood:	n/a	n/a
19	BRCA1	chr11:67373978-67374412	HepG2	liver:	n/a	n/a
20	BRCA1	chr11:67374249-67374557	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr11:67374196-67374580	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr11:67373619-67374645	K562	blood:	n/a	n/a
23	CCNT2	chr11:67374152-67374681	K562	blood:	n/a	n/a
24	CEBPB	chr11:67373906-67374578	GM12878	blood:	n/a	n/a
25	CEBPB	chr11:67374363-67374437	K562	blood:	n/a	n/a
26	CEBPB	chr11:67374216-67374519	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr11:67374083-67374560	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr11:67374057-67374582	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr11:67374120-67374597	HepG2	liver:	n/a	n/a
30	CHD2	chr11:67374067-67374652	GM12878	blood:	n/a	n/a
31	CHD2	chr11:67374212-67374536	K562	blood:	n/a	n/a
32	CREB1	chr11:67373983-67374802	K562	blood:	n/a	n/a
33	CREB1	chr11:67374096-67374748	ECC-1	luminal epithelium:	n/a	n/a
34	CREB1	chr11:67374025-67374744	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr11:67374032-67374660	A549	lung:	n/a	n/a
36	CREB1	chr11:67373822-67374837	GM12878	blood:	n/a	n/a
37	CREB1	chr11:67373866-67374766	HepG2	liver:	n/a	n/a
38	CREB1	chr11:67374185-67374585	A549	lung:	n/a	n/a
39	CREB1	chr11:67373900-67374881	GM12878	blood:	n/a	n/a
40	CREB1	chr11:67374074-67374773	ECC-1	luminal epithelium:	n/a	n/a
41	CREB1	chr11:67373969-67374870	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr11:67373739-67374835	HepG2	liver:	n/a	n/a
43	CREB1	chr11:67373971-67374931	K562	blood:	n/a	n/a
44	CTCF	chr11:67374300-67374450	BJ	skin:	n/a	chr11:67374388-67374404
45	CTCF	chr11:67374320-67374470	AG04450	lung:	n/a	chr11:67374388-67374404
46	CTCF	chr11:67374123-67374595	H1-hESC	embryonic stem cell:	n/a	chr11:67374212-67374225 chr11:67374388-67374404 chr11:67374299-67374312
47	CTCF	chr11:67374400-67374550	GM12873	blood:	n/a	n/a
48	CTCF	chr11:67374242-67374531	NHEK	skin:	n/a	chr11:67374388-67374404 chr11:67374299-67374312
49	CTCF	chr11:67374265-67374496	H1-hESC	embryonic stem cell:	n/a	chr11:67374388-67374404 chr11:67374299-67374312
50	CTCF	chr11:67374260-67374410	HEK293	kidney:	n/a	chr11:67374388-67374404 chr11:67374299-67374312

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67374151-67374201	HNPCEpiC	eye:	n/a
2	chr11:67374151-67374201	GM12892	blood:	n/a
3	chr11:67374151-67374201	T-47D	breast:	n/a
4	chr11:67374388-67374438	HEK293	kidney:	embryo
5	chr11:67374151-67374201	AG09319	gingival:	n/a
6	chr11:67374154-67374204	A549	lung:	n/a
7	chr11:67374151-67374201	U87	brain:	n/a
8	chr11:67374154-67374204	HCF	heart:	n/a
9	chr11:67374388-67374438	MCF-7	breast:	n/a
10	chr11:67374151-67374201	HUVEC	blood vessel:	n/a
11	chr11:67374388-67374438	NHBE	bronchial:	n/a
12	chr11:67374388-67374438	K562	blood:	n/a
13	chr11:67374151-67374201	Hepatocyte	liver:	n/a
14	chr11:67374388-67374438	PANC-1	pancreas:	n/a
15	chr11:67374213-67374263	BJ	skin:	n/a
16	chr11:67374151-67374201	GM12878	blood:	n/a
17	chr11:67374151-67374201	HCT-116	colon:	n/a
18	chr11:67374154-67374204	SAEC	small airway:	n/a
19	chr11:67374154-67374204	NHDF-neo	bronchial:	n/a
20	chr11:67374388-67374438	A549	lung:	n/a
21	chr11:67374213-67374263	HNPCEpiC	eye:	n/a
22	chr11:67374151-67374201	AoSMC	blood vessel:	n/a
23	chr11:67374154-67374204	PFSK-1	brain:	n/a
24	chr11:67374213-67374263	K562	blood:	n/a
25	chr11:67374151-67374201	NB4	blood:	n/a
26	chr11:67374151-67374201	AG10803	skin:	n/a
27	chr11:67374388-67374438	ProgFib	skin:	n/a
28	chr11:67374154-67374204	AG09319	gingival:	n/a
29	chr11:67374213-67374263	NH-A	brain:	n/a
30	chr11:67374388-67374438	GM12891	blood:	n/a
31	chr11:67374388-67374438	LNCaP	prostate:	n/a
32	chr11:67374213-67374263	BE2_C	brain:	n/a
33	chr11:67374154-67374204	AoSMC	blood vessel:	n/a
34	chr11:67374213-67374263	AG04449	skin:	fetal
35	chr11:67374213-67374263	Hepatocyte	liver:	n/a
36	chr11:67374388-67374438	HCT-116	colon:	n/a
37	chr11:67374154-67374204	GM19239	blood:	n/a
38	chr11:67374388-67374438	HNPCEpiC	eye:	n/a
39	chr11:67374213-67374263	A549	lung:	n/a
40	chr11:67374213-67374263	PANC-1	pancreas:	n/a
41	chr11:67374388-67374438	NHDF-neo	bronchial:	n/a
42	chr11:67374213-67374263	PFSK-1	brain:	n/a
43	chr11:67374213-67374263	HCM	heart:	n/a
44	chr11:67374388-67374438	BJ	skin:	n/a
45	chr11:67374151-67374201	A549	lung:	n/a
46	chr11:67374213-67374263	SAEC	small airway:	n/a
47	chr11:67374213-67374263	HPAEpiC	pulmonary alveolar:	n/a
48	chr11:67374151-67374201	AG09309	skin:	n/a
49	chr11:67374154-67374204	AG10803	skin:	n/a
50	chr11:67374213-67374263	LNCaP	prostate:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67372725..67386378-chr11:67392399..67400639,29	K562	blood:
2	chr11:67370584..67375680-chr11:67395595..67400853,11	MCF-7	breast:
3	chr11:67374284..67374841-chr15:65588149..65588820,2	HCT-116	colon:
4	chr11:67347249..67355748-chr11:67372717..67377095,16	K562	blood:
5	chr11:67250506..67252570-chr11:67374037..67375559,2	K562	blood:
6	chr11:67371375..67376389-chr11:67395488..67399117,10	K562	blood:
7	chr11:62620807..62623183-chr11:67373400..67376083,2	MCF-7	breast:
8	chr11:67274110..67276658-chr11:67374314..67376513,2	K562	blood:
9	chr11:67372115..67374476-chr17:19649917..19652325,2	MCF-7	breast:
10	chr11:67272696..67275492-chr11:67373280..67375901,2	MCF-7	breast:
11	chr11:67351259..67353873-chr11:67373020..67375265,2	MCF-7	breast:
12	chr11:67347575..67355744-chr11:67372717..67376912,13	K562	blood:
13	chr11:67271788..67274805-chr11:67372108..67375948,3	K562	blood:
14	chr11:67372621..67374795-chr17:19647401..19649907,2	MCF-7	breast:
15	chr11:67373358..67378331-chr11:67393882..67398214,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFV1-1	chr11:67373831-67374113	ENSG00000255119.1

No data

Variant related genes	Relation type
NDUFV1	TF binding region
C11orf72	TF binding region
NDUFV1	CpG island
C11orf72	CpG island
ENSG00000167799	chromatin interactions
ENSG00000255318	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000110711	chromatin interactions
ENSG00000108602	chromatin interactions
ENSG00000255717	chromatin interactions
ENSG00000084207	chromatin interactions
ENSG00000110697	chromatin interactions

Extended variants
information (count: 19 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560738622	chr11:67374095-67374096	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
2	rs73490567	chr11:67374105-67374106	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534692328	chr11:67374108-67374109	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
4	rs78309947	chr11:67374110-67374111	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
5	rs183695375	chr11:67374123-67374124	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs544906375	chr11:67374154-67374155	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs2514013	chr11:67374156-67374157	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575253948	chr11:67374178-67374179	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs376659189	chr11:67374230-67374231	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs542647739	chr11:67374244-67374245	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs560927277	chr11:67374252-67374253	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs145205309	chr11:67374279-67374280	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs540715639	chr11:67374292-67374293	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs565349535	chr11:67374293-67374294	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs149128474	chr11:67374330-67374331	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs551314520	chr11:67374347-67374348	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs563140258	chr11:67374365-67374366	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs373383800	chr11:67374402-67374403	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs549025720	chr11:67374408-67374409	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67373000-67374200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
2	chr11:67373200-67374200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr11:67373400-67374200	Flanking Active TSS	NHLF	lung
4	chr11:67373600-67374200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:67373600-67374200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:67373600-67374200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr11:67373600-67374200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
8	chr11:67373600-67374200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:67373600-67374200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:67373600-67374200	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr11:67373600-67374200	Flanking Active TSS	Liver	Liver
12	chr11:67373600-67374200	Flanking Active TSS	Brain Germinal Matrix	brain
13	chr11:67373600-67374200	Flanking Active TSS	Fetal Brain Male	brain
14	chr11:67373600-67374200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
15	chr11:67373600-67374200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
16	chr11:67373600-67374200	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr11:67373600-67374200	Flanking Active TSS	Dnd41	blood
18	chr11:67373600-67374200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr11:67373600-67374400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:67373600-67374800	Active TSS	Primary T helper naive cells from peripheral blood	blood
21	chr11:67373600-67374800	Active TSS	Fetal Brain Female	brain
22	chr11:67373600-67374800	Active TSS	Psoas Muscle	Psoas
23	chr11:67373600-67374800	Active TSS	Rectal Mucosa Donor 31	rectum
24	chr11:67373600-67375000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:67373600-67375000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
26	chr11:67373600-67375200	Active TSS	H9 Cell Line	embryonic stem cell
27	chr11:67373600-67375400	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr11:67373600-67375600	Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr11:67373600-67375600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chr11:67373800-67374200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
31	chr11:67373800-67374200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr11:67373800-67374200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr11:67373800-67374200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr11:67373800-67374200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:67373800-67374200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr11:67373800-67374200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr11:67373800-67374200	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr11:67373800-67374200	Flanking Active TSS	Primary hematopoietic stem cells	blood
39	chr11:67373800-67374200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
40	chr11:67373800-67374200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr11:67373800-67374200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr11:67373800-67374200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr11:67373800-67374200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr11:67373800-67374200	Flanking Active TSS	Fetal Muscle Trunk	muscle
45	chr11:67373800-67374200	Flanking Active TSS	Fetal Muscle Leg	muscle
46	chr11:67373800-67374200	Flanking Active TSS	Fetal Thymus	thymus
47	chr11:67373800-67374200	Flanking Active TSS	Hela-S3	cervix
48	chr11:67373800-67374200	Flanking Active TSS	HSMMtube	muscle
49	chr11:67373800-67374200	Flanking Active TSS	NH-A	brain
50	chr11:67373800-67374200	Flanking Active TSS	Osteobl	bone

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