Variant report

Variant	nsv897918
Chromosome Location	chr11:74757641-74798928
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:0)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:74797336-74797572	K562	blood:	n/a	n/a
2	ARID3A	chr11:74797976-74798342	K562	blood:	n/a	n/a
3	ARID3A	chr11:74770354-74770744	K562	blood:	n/a	n/a
4	ARID3A	chr11:74798550-74799308	K562	blood:	n/a	n/a
5	ATF3	chr11:74789276-74789456	K562	blood:	n/a	n/a
6	BHLHE40	chr11:74798454-74798668	K562	blood:	n/a	n/a
7	BHLHE40	chr11:74777236-74777328	K562	blood:	n/a	n/a
8	CBX3	chr11:74763431-74763841	K562	blood:	n/a	n/a
9	CBX3	chr11:74770312-74770748	K562	blood:	n/a	n/a
10	CCNT2	chr11:74770396-74770687	K562	blood:	n/a	n/a
11	CEBPB	chr11:74784555-74784879	K562	blood:	n/a	n/a
12	CEBPB	chr11:74784581-74784859	A549	lung:	n/a	n/a
13	CEBPB	chr11:74784551-74784892	IMR90	lung:	n/a	n/a
14	CEBPB	chr11:74764557-74764606	A549	lung:	n/a	n/a
15	CEBPB	chr11:74766611-74766903	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:74784621-74784748	K562	blood:	n/a	n/a
17	CEBPB	chr11:74784563-74784815	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr11:74767920-74768228	K562	blood:	n/a	chr11:74768054-74768065 chr11:74768067-74768078
19	CEBPB	chr11:74767886-74768246	Hela-S3	cervix:	n/a	chr11:74768054-74768065 chr11:74768067-74768078
20	CEBPB	chr11:74784555-74784893	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:74784575-74784840	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:74766597-74766887	A549	lung:	n/a	n/a
23	CEBPB	chr11:74795904-74795972	K562	blood:	n/a	n/a
24	CEBPB	chr11:74766601-74766844	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:74766731-74766786	K562	blood:	n/a	n/a
26	CEBPB	chr11:74767914-74768216	A549	lung:	n/a	chr11:74768054-74768065 chr11:74768067-74768078
27	CEBPB	chr11:74770514-74770757	K562	blood:	n/a	n/a
28	CEBPB	chr11:74767882-74768226	HepG2	liver:	n/a	chr11:74768054-74768065 chr11:74768067-74768078
29	CEBPB	chr11:74784590-74784861	MCF-7	breast:	n/a	n/a
30	CEBPD	chr11:74757755-74758002	K562	blood:	n/a	n/a
31	CTCF	chr11:74784980-74785130	GM12873	blood:	n/a	chr11:74785062-74785075 chr11:74785030-74785039
32	CTCF	chr11:74784920-74785070	HBMEC	blood vessel:	n/a	chr11:74785030-74785039
33	CTCF	chr11:74784980-74785130	HPAF	blood vessel:	n/a	chr11:74785062-74785075 chr11:74785030-74785039
34	CTCF	chr11:74784940-74785090	HepG2	liver:	n/a	chr11:74785062-74785075 chr11:74785030-74785039
35	CTCF	chr11:74784990-74785112	H1-hESC	embryonic stem cell:	n/a	chr11:74785062-74785075 chr11:74785030-74785039
36	CTCF	chr11:74785000-74785150	AoAF	blood vessel:	n/a	chr11:74785062-74785075 chr11:74785030-74785039
37	CTCF	chr11:74784880-74785030	GM12873	blood:	n/a	n/a
38	CTCF	chr11:74785000-74785150	HA-sp	spinal cord:	n/a	chr11:74785062-74785075 chr11:74785030-74785039
39	CTCF	chr11:74784847-74785241	K562	blood:	n/a	chr11:74785062-74785075 chr11:74785030-74785039
40	CTCF	chr11:74784740-74784890	RPTEC	kidney:	n/a	n/a
41	CTCF	chr11:74790780-74790930	GM12874	blood:	n/a	n/a
42	CTCF	chr11:74798480-74798662	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:74784900-74785050	GM12874	blood:	n/a	chr11:74785030-74785039
44	CTCF	chr11:74798416-74798715	K562	blood:	n/a	n/a
45	CTCF	chr11:74784798-74785265	K562	blood:	n/a	chr11:74785062-74785075 chr11:74785030-74785039
46	CTCF	chr11:74777460-74777610	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:74785000-74785150	HRPEpiC	eye:	n/a	chr11:74785062-74785075 chr11:74785030-74785039
48	CTCF	chr11:74798480-74798630	K562	blood:	n/a	n/a
49	CTCF	chr11:74798340-74798490	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr11:74784940-74785090	GM12872	blood:	n/a	chr11:74785062-74785075 chr11:74785030-74785039

No data

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:74796178..74800020-chr11:74800917..74805286,4	K562	blood:
2	chr11:74761657..74763854-chr11:74765493..74768337,2	K562	blood:
3	chr11:74781895..74783678-chr11:74787128..74789596,2	K562	blood:
4	chr11:74795794..74798553-chr11:74813017..74814712,2	K562	blood:
5	chr11:74777918..74780984-chr11:74782589..74785289,3	K562	blood:
6	chr11:74742464..74743172-chr11:74783405..74784082,2	K562	blood:
7	chr11:74764412..74766619-chr11:74774749..74776362,2	MCF-7	breast:
8	chr11:74770127..74772846-chr11:74773872..74776209,2	K562	blood:
9	chr11:74775284..74777125-chr11:74778388..74781145,2	K562	blood:
10	chr11:74772361..74774427-chr11:74774616..74776750,2	K562	blood:
11	chr11:74775844..74777522-chr11:74789368..74791115,2	K562	blood:
12	chr11:74772361..74774427-chr11:74774616..74776750,2	K562	blood:
13	chr11:74699633..74701606-chr11:74779257..74781418,2	K562	blood:
14	chr11:74761657..74763854-chr11:74765493..74768337,2	K562	blood:
15	chr11:74775284..74777125-chr11:74778388..74781145,2	K562	blood:
16	chr11:74767988..74770673-chr11:75062198..75065029,2	K562	blood:
17	chr11:74764412..74766619-chr11:74774749..74776362,2	MCF-7	breast:
18	chr11:74773998..74776628-chr11:74806307..74808054,2	K562	blood:
19	chr11:74768855..74771237-chr11:74780461..74783497,3	MCF-7	breast:
20	chr11:74777918..74781426-chr11:74782589..74786387,4	K562	blood:
21	chr11:74776958..74778685-chr11:74780199..74782834,2	MCF-7	breast:
22	chr11:74770400..74772058-chr11:74780541..74783446,2	K562	blood:
23	chr11:74733675..74734283-chr11:74784742..74785495,2	MCF-7	breast:
24	chr11:74762519..74764058-chr11:74769921..74771618,2	K562	blood:
25	chr11:74770127..74772846-chr11:74773872..74776209,2	K562	blood:
26	chr11:74784418..74786926-chr11:74788706..74790951,2	K562	blood:
27	chr11:74784418..74786926-chr11:74788706..74790951,2	K562	blood:
28	chr11:74775986..74778736-chr11:74786345..74788649,2	K562	blood:
29	chr11:74776958..74778685-chr11:74780199..74782834,2	MCF-7	breast:
30	chr11:74775844..74777522-chr11:74789368..74791115,2	K562	blood:
31	chr11:74798344..74800296-chr11:74811269..74812884,2	K562	blood:
32	chr11:74762519..74764058-chr11:74769921..74771618,2	K562	blood:
33	chr11:74720213..74722321-chr11:74770764..74773550,2	K562	blood:
34	chr11:74775986..74778736-chr11:74786345..74788649,2	K562	blood:
35	chr11:74769145..74771076-chr11:74811146..74813456,2	K562	blood:

No data

Variant related genes	Relation type
NPM1P50	TF binding region
OR2AT2P	TF binding region
ENSG00000137491	chromatin interactions
ENSG00000234611	chromatin interactions
ENSG00000162139	chromatin interactions
ENSG00000137486	chromatin interactions

Extended variants
information (count: 1331 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1331 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7941838	chr11:74757641-74757642	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373570824	chr11:74757660-74757661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567740742	chr11:74757664-74757665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551431706	chr11:74757675-74757676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11236307	chr11:74757786-74757787	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs185459664	chr11:74757800-74757801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555987959	chr11:74757823-74757824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141634582	chr11:74757832-74757833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370972501	chr11:74757857-74757858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546707078	chr11:74757864-74757865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575626113	chr11:74757875-74757876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555515001	chr11:74757888-74757889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144517554	chr11:74757900-74757901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555091256	chr11:74757991-74757992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7929665	chr11:74757999-74758000	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs190121760	chr11:74758046-74758047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148451638	chr11:74758059-74758060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572824239	chr11:74758080-74758081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544571435	chr11:74758086-74758087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182076131	chr11:74758121-74758122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530558894	chr11:74758127-74758128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550403983	chr11:74758134-74758135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561081303	chr11:74758156-74758157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530278530	chr11:74758157-74758158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185134723	chr11:74758220-74758221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541041997	chr11:74758226-74758227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112392957	chr11:74758245-74758246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113132290	chr11:74758249-74758250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556290940	chr11:74758270-74758271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116794028	chr11:74758275-74758276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569154682	chr11:74758372-74758373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374078764	chr11:74758403-74758404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538278589	chr11:74758417-74758418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554724466	chr11:74758457-74758458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183968655	chr11:74758487-74758488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs118104118	chr11:74758504-74758505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552766832	chr11:74758566-74758567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572735897	chr11:74758568-74758569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544954146	chr11:74758602-74758603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565232536	chr11:74758672-74758673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575124059	chr11:74758770-74758771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544205912	chr11:74758840-74758841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376680586	chr11:74758917-74758918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367887627	chr11:74758979-74758980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188912615	chr11:74759003-74759004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529827769	chr11:74759101-74759102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141750286	chr11:74759167-74759168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7112525	chr11:74759185-74759186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs193084779	chr11:74759301-74759302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552584866	chr11:74759325-74759326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74756200-74761200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:74756400-74758000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:74756400-74758000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:74756600-74759000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:74757000-74757800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr11:74757000-74762200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:74757200-74758000	Weak transcription	Placenta	Placenta
8	chr11:74757200-74758400	Enhancers	K562	blood
9	chr11:74758000-74758200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr11:74758000-74758200	Enhancers	Placenta	Placenta
11	chr11:74758000-74758400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr11:74758000-74758400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr11:74758000-74758400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr11:74758200-74758600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:74759400-74761800	Enhancers	GM12878-XiMat	blood
16	chr11:74760400-74761200	Enhancers	Primary B cells from cord blood	blood
17	chr11:74760400-74762200	Enhancers	Primary B cells from peripheral blood	blood
18	chr11:74761200-74761400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr11:74761200-74762000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr11:74761400-74762400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:74761800-74762600	ZNF genes & repeats	GM12878-XiMat	blood
22	chr11:74762000-74762400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr11:74762200-74762400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr11:74762400-74766200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr11:74762400-74771000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:74765200-74765600	Enhancers	HSMMtube	muscle
27	chr11:74766200-74766800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr11:74766200-74767400	Enhancers	Placenta	Placenta
29	chr11:74766800-74767200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr11:74767200-74767400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr11:74767200-74768200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr11:74767400-74771000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr11:74768200-74769400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr11:74769400-74770200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr11:74769400-74771000	Enhancers	K562	blood
36	chr11:74769600-74771400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr11:74771000-74771200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:74771000-74771200	Flanking Active TSS	K562	blood
39	chr11:74771000-74771400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr11:74771200-74771600	Enhancers	K562	blood
41	chr11:74771400-74773400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:74771400-74774800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr11:74773400-74773800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:74773600-74773800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:74773800-74774800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:74773800-74782200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr11:74774800-74775200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:74774800-74775400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr11:74775000-74775200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:74775000-74775200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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