Variant report

Variant	nsv977615
Chromosome Location	chr14:20643351-20673001
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:245)
CpG islands
(count:185)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20644582-20645133	K562	blood:	n/a	n/a
2	ARID3A	chr14:20645562-20646086	K562	blood:	n/a	n/a
3	ATF1	chr14:20645594-20645932	K562	blood:	n/a	n/a
4	ATF3	chr14:20645584-20645910	K562	blood:	n/a	n/a
5	BHLHE40	chr14:20645542-20646303	K562	blood:	n/a	n/a
6	BHLHE40	chr14:20653018-20653080	K562	blood:	n/a	n/a
7	CBX3	chr14:20645492-20645863	K562	blood:	n/a	n/a
8	CBX3	chr14:20645515-20645980	K562	blood:	n/a	n/a
9	CCNT2	chr14:20645714-20646195	K562	blood:	n/a	n/a
10	CEBPB	chr14:20644555-20644849	K562	blood:	n/a	chr14:20644780-20644791 chr14:20644718-20644735 chr14:20644780-20644791
11	CEBPB	chr14:20645573-20645988	K562	blood:	n/a	n/a
12	CEBPB	chr14:20659063-20659394	HepG2	liver:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
13	CEBPB	chr14:20668546-20668738	A549	lung:	n/a	n/a
14	CEBPB	chr14:20667271-20667577	Hela-S3	cervix:	n/a	chr14:20667443-20667454
15	CEBPB	chr14:20667283-20667629	HepG2	liver:	n/a	chr14:20667443-20667454
16	CEBPB	chr14:20667315-20667568	K562	blood:	n/a	chr14:20667443-20667454
17	CEBPB	chr14:20668608-20668745	K562	blood:	n/a	n/a
18	CEBPB	chr14:20643233-20643506	K562	blood:	n/a	chr14:20643311-20643324
19	CEBPB	chr14:20659170-20659372	K562	blood:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
20	CEBPB	chr14:20645527-20645985	K562	blood:	n/a	n/a
21	CEBPB	chr14:20667315-20667616	A549	lung:	n/a	chr14:20667443-20667454
22	CEBPB	chr14:20644548-20644852	K562	blood:	n/a	chr14:20644780-20644791 chr14:20644718-20644735 chr14:20644780-20644791
23	CEBPB	chr14:20652454-20652480	HepG2	liver:	n/a	n/a
24	CEBPD	chr14:20645540-20645977	K562	blood:	n/a	n/a
25	CEBPD	chr14:20645568-20646098	K562	blood:	n/a	n/a
26	CHD2	chr14:20662444-20662449	GM12878	blood:	n/a	n/a
27	CTCF	chr14:20669388-20669474	MCF-7	breast:	n/a	n/a
28	CTCF	chr14:20664241-20664344	ProgFib	skin:	n/a	n/a
29	CTCF	chr14:20664160-20664310	HEK293	kidney:	n/a	n/a
30	CTCF	chr14:20664194-20664358	MCF-7	breast:	n/a	n/a
31	CTCF	chr14:20664300-20664450	HCT-116	colon:	n/a	n/a
32	CTCF	chr14:20664140-20664290	HMEC	breast:	n/a	n/a
33	CTCF	chr14:20664080-20664230	HCT-116	colon:	n/a	n/a
34	CTCF	chr14:20664120-20664270	HepG2	liver:	n/a	n/a
35	CTCF	chr14:20664180-20664330	K562	blood:	n/a	n/a
36	CTCF	chr14:20664169-20664172	LNCaP	prostate:	n/a	n/a
37	CTCF	chr14:20664148-20664387	K562	blood:	n/a	n/a
38	CTCF	chr14:20658542-20658731	K562	blood:	n/a	n/a
39	CTCF	chr14:20664232-20664277	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr14:20664160-20664310	MCF-7	breast:	n/a	n/a
41	CTCF	chr14:20664200-20664350	NB4	blood:	n/a	n/a
42	CTCF	chr14:20664180-20664330	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr14:20643673-20643693	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr14:20664209-20664369	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:20664280-20664430	BE2_C	brain:	n/a	n/a
46	CTCF	chr14:20643633-20643708	LNCaP	prostate:	n/a	n/a
47	CTCF	chr14:20664160-20664310	HL-60	blood:	n/a	n/a
48	CTCF	chr14:20658599-20658709	K562	blood:	n/a	n/a
49	CTCF	chr14:20664260-20664410	K562	blood:	n/a	n/a
50	CTCF	chr14:20664220-20664370	MCF-7	breast:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20664580-20664630	HRCEpiC	kidney:	n/a
2	chr14:20664580-20664630	NH-A	brain:	n/a
3	chr14:20664580-20664630	HRCEpiC	kidney:	n/a
4	chr14:20664580-20664630	NH-A	brain:	n/a
5	chr14:20666088-20666138	K562	blood:	n/a
6	chr14:20664021-20664071	Caco-2	colon:	n/a
7	chr14:20666088-20666138	HCT-116	colon:	n/a
8	chr14:20664580-20664630	NB4	blood:	n/a
9	chr14:20664580-20664630	HEEpiC	esophagus:	n/a
10	chr14:20664580-20664630	ProgFib	skin:	n/a
11	chr14:20664580-20664630	AG04450	lung:	fetal
12	chr14:20666088-20666138	HRCEpiC	kidney:	n/a
13	chr14:20666088-20666138	PrEC	prostate:	n/a
14	chr14:20664021-20664071	GM12878	blood:	n/a
15	chr14:20666088-20666138	HAEpiC	amniotic membrane:	n/a
16	chr14:20664580-20664630	T-47D	breast:	n/a
17	chr14:20664021-20664071	MCF-7	breast:	n/a
18	chr14:20664580-20664630	GM12878	blood:	n/a
19	chr14:20664580-20664630	RPTEC	kidney:	n/a
20	chr14:20664580-20664630	GM12891	blood:	n/a
21	chr14:20666088-20666138	GM19239	blood:	n/a
22	chr14:20664580-20664630	GM12892	blood:	n/a
23	chr14:20666088-20666138	GM06990	blood:	n/a
24	chr14:20664021-20664071	HL-60	blood:	n/a
25	chr14:20666088-20666138	HNPCEpiC	eye:	n/a
26	chr14:20664021-20664071	SK-N-SH	brain:	n/a
27	chr14:20664580-20664630	HCM	heart:	n/a
28	chr14:20664021-20664071	SK-N-SH_RA	brain:	n/a
29	chr14:20664580-20664630	HCT-116	colon:	n/a
30	chr14:20664021-20664071	NHBE	bronchial:	n/a
31	chr14:20664580-20664630	SK-N-SH	brain:	n/a
32	chr14:20666088-20666138	T-47D	breast:	n/a
33	chr14:20664580-20664630	BE2_C	brain:	n/a
34	chr14:20664580-20664630	HPAEpiC	pulmonary alveolar:	n/a
35	chr14:20664021-20664071	HMEC	breast:	n/a
36	chr14:20664580-20664630	Jurkat	blood:	n/a
37	chr14:20666088-20666138	RPTEC	kidney:	n/a
38	chr14:20666088-20666138	NHBE	bronchial:	n/a
39	chr14:20664580-20664630	SK-N-SH_RA	brain:	n/a
40	chr14:20664021-20664071	HEEpiC	esophagus:	n/a
41	chr14:20664021-20664071	A549	lung:	n/a
42	chr14:20666088-20666138	MCF10A-Er-Src	breast:	n/a
43	chr14:20664021-20664071	U87	brain:	n/a
44	chr14:20664580-20664630	PrEC	prostate:	n/a
45	chr14:20664580-20664630	NT2-D1	testis:	n/a
46	chr14:20664021-20664071	NH-A	brain:	n/a
47	chr14:20664580-20664630	NHDF-neo	bronchial:	n/a
48	chr14:20664580-20664630	HRPEpiC	eye:	n/a
49	chr14:20664021-20664071	LNCaP	prostate:	n/a
50	chr14:20664580-20664630	Hepatocyte	liver:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20642540..20645135-chr14:20796578..20798741,2	K562	blood:
2	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
3	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:
4	chr14:20583619..20586533-chr14:20649310..20650931,2	K562	blood:
5	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
6	chr14:20645666..20648683-chr14:20649468..20653312,5	K562	blood:
7	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
8	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
9	chr14:20645875..20648132-chr14:20651152..20653312,3	K562	blood:
10	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
11	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
12	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
13	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:

No data

Variant related genes	Relation type
OR11H5P	TF binding region
OR11G1P	TF binding region
OR11G2	TF binding region
ENSG00000259095	TF binding region
OR11H5P	CpG island
OR11G1P	CpG island
OR11G2	CpG island
ENSG00000259095	CpG island
ENSG00000176230	chromatin interactions
ENSG00000258468	chromatin interactions
ENSG00000100814	chromatin interactions

Extended variants
information (count: 633 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536462347	chr14:20643356-20643357	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs536397071	chr14:20643357-20643358	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs376590597	chr14:20643381-20643382	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs555018983	chr14:20643389-20643390	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs573259965	chr14:20643404-20643405	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs60068674	chr14:20643409-20643410	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs148601023	chr14:20643422-20643423	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs576855621	chr14:20643423-20643424	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs544086340	chr14:20643440-20643441	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs117200913	chr14:20643443-20643444	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs529873309	chr14:20643461-20643462	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs548088506	chr14:20643467-20643468	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs116016431	chr14:20643556-20643557	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs537725211	chr14:20643564-20643565	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs181381050	chr14:20643568-20643569	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs113743445	chr14:20643570-20643571	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs552346049	chr14:20643599-20643600	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs186417638	chr14:20643605-20643606	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs562742645	chr14:20643612-20643613	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs537872104	chr14:20643624-20643625	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs551258926	chr14:20643634-20643635	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs191945428	chr14:20643638-20643639	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs202035624	chr14:20643681-20643682	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs75800027	chr14:20643685-20643686	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs554872098	chr14:20643731-20643732	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs567092552	chr14:20643737-20643738	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs534008409	chr14:20643774-20643775	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs7142335	chr14:20643775-20643776	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs576791960	chr14:20643841-20643842	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs71410211	chr14:20643843-20643844	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs7156279	chr14:20643847-20643848	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs182953734	chr14:20643864-20643865	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs187541661	chr14:20643898-20643899	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7160752	chr14:20643903-20643904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560088198	chr14:20643930-20643931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113524915	chr14:20643934-20643935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545897110	chr14:20643970-20643971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs527779499	chr14:20643976-20643977	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs986364	chr14:20644026-20644027	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs531304627	chr14:20644045-20644046	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs549514378	chr14:20644050-20644051	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs72669084	chr14:20644078-20644079	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs78032264	chr14:20644133-20644134	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs543678741	chr14:20644228-20644229	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs548893619	chr14:20644303-20644304	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs76954510	chr14:20644318-20644319	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs986365	chr14:20644322-20644323	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs115319720	chr14:20644357-20644358	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs570619100	chr14:20644388-20644389	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs986366	chr14:20644436-20644437	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20643000-20644000	Enhancers	K562	blood
2	chr14:20643400-20643600	Enhancers	Pancreas	Pancrea
3	chr14:20643400-20643800	Enhancers	Stomach Mucosa	stomach
4	chr14:20643800-20645200	Weak transcription	Pancreas	Pancrea
5	chr14:20644000-20644200	Flanking Active TSS	K562	blood
6	chr14:20644200-20644400	Enhancers	Stomach Mucosa	stomach
7	chr14:20644200-20644600	Enhancers	K562	blood
8	chr14:20644600-20644800	Flanking Active TSS	K562	blood
9	chr14:20644800-20645000	Enhancers	K562	blood
10	chr14:20645000-20645200	Flanking Active TSS	K562	blood
11	chr14:20645200-20645800	Enhancers	K562	blood
12	chr14:20645200-20646400	Enhancers	Pancreas	Pancrea
13	chr14:20645800-20646400	Flanking Active TSS	K562	blood
14	chr14:20646000-20648200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:20646000-20649000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr14:20646200-20646400	Enhancers	Primary hematopoietic stem cells	blood
17	chr14:20646400-20647400	Weak transcription	Pancreas	Pancrea
18	chr14:20646400-20648400	Enhancers	K562	blood
19	chr14:20646800-20647400	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr14:20647000-20647800	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr14:20647400-20647600	ZNF genes & repeats	Pancreas	Pancrea
22	chr14:20647400-20648200	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr14:20647400-20648400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr14:20647600-20648200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr14:20647600-20650400	Weak transcription	Pancreas	Pancrea
26	chr14:20647800-20648200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
27	chr14:20648000-20648400	Enhancers	Primary hematopoietic stem cells	blood
28	chr14:20648200-20649800	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr14:20648400-20648800	Weak transcription	K562	blood
30	chr14:20648400-20648800	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr14:20648800-20649000	Enhancers	K562	blood
32	chr14:20648800-20649200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr14:20649000-20650400	Weak transcription	K562	blood
34	chr14:20649200-20649600	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr14:20650000-20650400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr14:20650400-20651000	Enhancers	K562	blood
37	chr14:20651000-20652400	Weak transcription	K562	blood
38	chr14:20652400-20653200	Enhancers	K562	blood
39	chr14:20663200-20664600	Enhancers	K562	blood
40	chr14:20664200-20666400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr14:20665600-20666400	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr14:20665800-20666400	Enhancers	Primary neutrophils fromperipheralblood	blood

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