Variant report

Variant	esv3524007
Chromosome Location	chr14:81876199-81882597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:24)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:24 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr14:81882467-81883015	K562	blood:	n/a	n/a
2	CEBPB	chr14:81878924-81879121	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr14:81878850-81879176	A549	lung:	n/a	n/a
4	CEBPB	chr14:81878895-81879151	K562	blood:	n/a	n/a
5	CEBPB	chr14:81878865-81879164	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr14:81878944-81879032	IMR90	lung:	n/a	n/a
7	CTCF	chr14:81879565-81879655	Lung_OC	lung:	n/a	n/a
8	CTCF	chr14:81879369-81879450	ProgFib	skin:	n/a	n/a
9	ELF1	chr14:81882593-81882843	K562	blood:	n/a	chr14:81882679-81882692 chr14:81882730-81882743
10	EP300	chr14:81882585-81883581	K562	blood:	n/a	chr14:81882733-81882742 chr14:81882681-81882695
11	ESR1	chr14:81879118-81879383	ECC-1	luminal epithelium:	n/a	n/a
12	IRF1	chr14:81882464-81883231	K562	blood:	n/a	chr14:81882687-81882698 chr14:81882686-81882700 chr14:81882686-81882696 chr14:81882685-81882694
13	MAFK	chr14:81882429-81882897	K562	blood:	n/a	chr14:81882648-81882662
14	MAZ	chr14:81881715-81881775	HepG2	liver:	n/a	n/a
15	MYC	chr14:81882526-81882756	K562	blood:	n/a	n/a
16	POLR2A	chr14:81882235-81882292	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr14:81876348-81876459	K562	blood:	n/a	n/a
18	POLR2A	chr14:81878168-81878329	K562	blood:	n/a	n/a
19	RCOR1	chr14:81882349-81883689	K562	blood:	n/a	n/a
20	SPI1	chr14:81882437-81882916	HL-60	blood:	n/a	chr14:81882686-81882695 chr14:81882731-81882744 chr14:81882730-81882743
21	TBL1XR1	chr14:81882532-81882717	K562	blood:	n/a	n/a
22	TEAD4	chr14:81882437-81882919	K562	blood:	n/a	n/a
23	YY1	chr14:81879145-81879402	ECC-1	luminal epithelium:	n/a	n/a
24	ZNF384	chr14:81876677-81876690	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81879375-81879425	PANC-1	pancreas:	n/a
2	chr14:81879247-81879297	SK-N-SH	brain:	n/a
3	chr14:81879375-81879425	T-47D	breast:	n/a
4	chr14:81879247-81879297	PANC-1	pancreas:	n/a
5	chr14:81879375-81879425	CMK	blood:	n/a
6	chr14:81879247-81879297	ProgFib	skin:	n/a
7	chr14:81879375-81879425	AG04450	lung:	fetal
8	chr14:81879247-81879297	SKMC	muscle:	n/a
9	chr14:81879247-81879297	HMEC	breast:	n/a
10	chr14:81879375-81879425	A549	lung:	n/a
11	chr14:81879375-81879425	H1-hESC	embryonic stem cell:	embryo
12	chr14:81879375-81879425	MCF10A-Er-Src	breast:	n/a
13	chr14:81879375-81879425	BE2_C	brain:	n/a
14	chr14:81879247-81879297	SAEC	small airway:	n/a
15	chr14:81879375-81879425	NHBE	bronchial:	n/a
16	chr14:81879247-81879297	BE2_C	brain:	n/a
17	chr14:81879247-81879297	AG09319	gingival:	n/a
18	chr14:81879247-81879297	SK-N-MC	brain:	n/a
19	chr14:81879247-81879297	AG10803	skin:	n/a
20	chr14:81879247-81879297	Hepatocyte	liver:	n/a
21	chr14:81879375-81879425	HL-60	blood:	n/a
22	chr14:81879247-81879297	HEEpiC	esophagus:	n/a
23	chr14:81879247-81879297	NB4	blood:	n/a
24	chr14:81879247-81879297	U87	brain:	n/a
25	chr14:81879247-81879297	HepG2	liver:	n/a
26	chr14:81879247-81879297	NH-A	brain:	n/a
27	chr14:81879375-81879425	GM12892	blood:	n/a
28	chr14:81879247-81879297	HRE	kidney:	n/a
29	chr14:81879247-81879297	NT2-D1	testis:	n/a
30	chr14:81879375-81879425	HepG2	liver:	n/a
31	chr14:81879375-81879425	HCPEpiC	choroid plexus:	n/a
32	chr14:81879247-81879297	LNCaP	prostate:	n/a
33	chr14:81879247-81879297	HEK293	kidney:	embryo
34	chr14:81879247-81879297	A549	lung:	n/a
35	chr14:81879375-81879425	NHDF-neo	bronchial:	n/a
36	chr14:81879375-81879425	Hela-S3	cervix:	n/a
37	chr14:81879247-81879297	T-47D	breast:	n/a
38	chr14:81879375-81879425	HNPCEpiC	eye:	n/a
39	chr14:81879375-81879425	HCM	heart:	n/a
40	chr14:81879375-81879425	MCF-7	breast:	n/a
41	chr14:81879375-81879425	HUVEC	blood vessel:	n/a
42	chr14:81879247-81879297	RPTEC	kidney:	n/a
43	chr14:81879247-81879297	Jurkat	blood:	n/a
44	chr14:81879247-81879297	PFSK-1	brain:	n/a
45	chr14:81879247-81879297	ECC-1	luminal epithelium:	n/a
46	chr14:81879375-81879425	HPAEpiC	pulmonary alveolar:	n/a
47	chr14:81879375-81879425	NB4	blood:	n/a
48	chr14:81879375-81879425	SK-N-SH_RA	brain:	n/a
49	chr14:81879375-81879425	AoSMC	blood vessel:	n/a
50	chr14:81879375-81879425	HAEpiC	amniotic membrane:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:81684469..81687360-chr14:81875537..81877645,3	K562	blood:
2	chr14:81876407..81878625-chr14:81895373..81897999,2	K562	blood:
3	chr14:81876702..81879078-chr14:81892366..81894170,2	K562	blood:
4	chr14:81871493..81873378-chr14:81876007..81877708,2	K562	blood:
5	chr14:81875040..81877398-chr14:81879695..81881536,2	K562	blood:
6	chr14:81875040..81877398-chr14:81879695..81881536,2	K562	blood:
7	chr14:81880605..81883337-chr14:81885961..81888667,2	K562	blood:
8	chr14:81871880..81873578-chr14:81882062..81884053,2	MCF-7	breast:
9	chr14:81685691..81688551-chr14:81879364..81882605,3	K562	blood:
10	chr14:81685671..81687321-chr14:81879290..81881702,3	MCF-7	breast:
11	chr14:81870339..81872408-chr14:81882068..81884278,2	K562	blood:
12	chr14:81684550..81687395-chr14:81881105..81883883,2	K562	blood:
13	chr14:81867720..81869556-chr14:81873808..81876587,2	MCF-7	breast:
14	chr14:81881608..81884227-chr14:81901358..81903544,2	K562	blood:
15	chr14:81867994..81870092-chr14:81876125..81877918,2	K562	blood:
16	chr14:81862798..81865439-chr14:81880673..81882798,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEL1L-11	chr14:81881291-81881385	NONHSAT038064

No data

Variant related genes	Relation type
ENSG00000258605	TF binding region
ENSG00000258605	CpG island
ENSG00000140022	chromatin interactions
ENSG00000165417	chromatin interactions

Extended variants
information (count: 248 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:248 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535035722	chr14:81876205-81876206	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs3844533	chr14:81876260-81876261	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541344447	chr14:81876297-81876298	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575120491	chr14:81876303-81876304	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569846844	chr14:81876335-81876336	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs377085828	chr14:81876357-81876358	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs28637476	chr14:81876368-81876369	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs3844534	chr14:81876396-81876397	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs71416867	chr14:81876437-81876438	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576032999	chr14:81876443-81876444	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs577935115	chr14:81876457-81876458	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs34661653	chr14:81876478-81876479	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140440306	chr14:81876497-81876498	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs8016935	chr14:81876515-81876516	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs576387235	chr14:81876575-81876576	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76903403	chr14:81876621-81876622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs559384117	chr14:81876642-81876643	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530046726	chr14:81876664-81876665	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541645071	chr14:81876672-81876673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs563528723	chr14:81876871-81876872	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs530641838	chr14:81876878-81876879	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs552672526	chr14:81876891-81876892	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs545943706	chr14:81876930-81876931	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs146438667	chr14:81876932-81876933	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs140752687	chr14:81876936-81876937	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs150116778	chr14:81876944-81876945	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs568900551	chr14:81876995-81876996	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs79456556	chr14:81877087-81877088	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs557390592	chr14:81877096-81877097	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs138426340	chr14:81877099-81877100	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs17111790	chr14:81877107-81877108	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs377493575	chr14:81877123-81877124	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs369886497	chr14:81877127-81877128	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs545702119	chr14:81877155-81877156	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs563704669	chr14:81877157-81877158	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs187537322	chr14:81877178-81877179	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs575409056	chr14:81877236-81877237	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs35663993	chr14:81877263-81877264	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs550138010	chr14:81877277-81877278	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542844093	chr14:81877317-81877318	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs540616000	chr14:81877330-81877331	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs552969302	chr14:81877351-81877352	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs531445258	chr14:81877355-81877356	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs561946643	chr14:81877370-81877371	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs542082318	chr14:81877371-81877372	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs8022070	chr14:81877382-81877383	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs377323156	chr14:81877439-81877440	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs530685912	chr14:81877473-81877474	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs546064735	chr14:81877493-81877494	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs564559995	chr14:81877509-81877510	Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81836400-81885800	Weak transcription	Gastric	stomach
2	chr14:81852800-81899800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:81861400-81889400	Weak transcription	Fetal Kidney	kidney
4	chr14:81862800-81881400	Weak transcription	Fetal Intestine Small	intestine
5	chr14:81864400-81893600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr14:81865000-81884600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:81865000-81885600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr14:81865000-81889400	Weak transcription	Ovary	ovary
9	chr14:81865000-81892400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr14:81867600-81892000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr14:81867800-81889800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr14:81868400-81884000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr14:81868800-81881600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr14:81868800-81893600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:81869200-81879200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr14:81869400-81880600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr14:81872200-81876800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr14:81873400-81879200	Weak transcription	Placenta	Placenta
19	chr14:81873400-81880400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr14:81873600-81878400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr14:81873600-81878400	Weak transcription	HSMMtube	muscle
22	chr14:81873600-81886000	Weak transcription	Fetal Muscle Leg	muscle
23	chr14:81874000-81876800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:81874000-81880400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr14:81874000-81880800	Weak transcription	Psoas Muscle	Psoas
26	chr14:81874000-81882800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr14:81874400-81882600	Weak transcription	Adipose Nuclei	Adipose
28	chr14:81874800-81892600	Weak transcription	Hela-S3	cervix
29	chr14:81875200-81876800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:81876000-81876200	Genic enhancers	K562	blood
31	chr14:81876200-81876400	Enhancers	K562	blood
32	chr14:81876400-81878600	Weak transcription	K562	blood
33	chr14:81876800-81877600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
34	chr14:81876800-81877800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:81876800-81877800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr14:81876800-81884200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr14:81877600-81879200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr14:81877800-81878600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr14:81877800-81879200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:81877800-81879200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr14:81878400-81879800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr14:81878600-81879600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
43	chr14:81878600-81881200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr14:81878600-81882000	Strong transcription	K562	blood
45	chr14:81878800-81879200	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr14:81878800-81879400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr14:81879200-81879400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr14:81879200-81879400	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr14:81879200-81879400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr14:81879200-81879400	Bivalent Enhancer	Placenta	Placenta

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