Variant report

Variant	nsv901480
Chromosome Location	chr14:22221211-22255090
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:22236446-22236646	K562	blood:	n/a	n/a
2	BACH1	chr14:22239915-22240160	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:22236428-22236693	K562	blood:	n/a	n/a
4	BHLHE40	chr14:22236359-22236692	GM12878	blood:	n/a	n/a
5	CEBPB	chr14:22249065-22249134	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:22249926-22250066	HepG2	liver:	n/a	n/a
7	CTCF	chr14:22236080-22236230	HRPEpiC	eye:	n/a	n/a
8	CTCF	chr14:22236460-22236610	GM12872	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
9	CTCF	chr14:22236500-22236650	RPTEC	kidney:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
10	CTCF	chr14:22236560-22236710	HCT-116	colon:	n/a	n/a
11	CTCF	chr14:22236480-22236630	GM12865	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
12	CTCF	chr14:22236460-22236610	GM12865	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
13	CTCF	chr14:22236441-22236685	Gliobla	brain:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
14	CTCF	chr14:22236509-22236686	GM19238	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
15	CTCF	chr14:22236475-22236687	A549	lung:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
16	CTCF	chr14:22236560-22236710	HAc	cerebellar:	n/a	n/a
17	CTCF	chr14:22236480-22236630	GM12801	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
18	CTCF	chr14:22236780-22236930	GM12874	blood:	n/a	n/a
19	CTCF	chr14:22236460-22236610	AG04449	skin:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
20	CTCF	chr14:22236367-22236749	K562	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
21	CTCF	chr14:22236440-22236590	GM12869	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
22	CTCF	chr14:22236500-22236650	HMF	breast:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
23	CTCF	chr14:22236480-22236630	RPTEC	kidney:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
24	CTCF	chr14:22236492-22236658	GM19240	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
25	CTCF	chr14:22236500-22236650	SAEC	small airway:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
26	CTCF	chr14:22236434-22236696	MCF-7	breast:	n/a	chr14:22236545-22236566 chr14:22236543-22236561 chr14:22236544-22236560
27	CTCF	chr14:22236480-22236630	GM12875	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
28	CTCF	chr14:22236500-22236650	Hela-S3	cervix:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
29	CTCF	chr14:22236500-22236650	NHLF	lung:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
30	CTCF	chr14:22236440-22236590	AG10803	skin:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
31	CTCF	chr14:22236520-22236670	GM12864	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
32	CTCF	chr14:22236480-22236630	GM12864	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
33	CTCF	chr14:22236480-22236630	MCF-7	breast:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
34	CTCF	chr14:22236467-22236624	SK-N-SH_RA	brain:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
35	CTCF	chr14:22236480-22236630	AoAF	blood vessel:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
36	CTCF	chr14:22236480-22236630	HPAF	blood vessel:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
37	CTCF	chr14:22236520-22236670	WERI-Rb-1	eye:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
38	CTCF	chr14:22236365-22236751	GM12878	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
39	CTCF	chr14:22236500-22236650	GM12867	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
40	CTCF	chr14:22236520-22236670	HCFaa	heart:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
41	CTCF	chr14:22236493-22236628	Pancreas_OC	pancreas:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
42	CTCF	chr14:22236440-22236590	HRE	kidney:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
43	CTCF	chr14:22236431-22236674	K562	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
44	CTCF	chr14:22236460-22236610	NHDF-neo	bronchial:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
45	CTCF	chr14:22236500-22236650	GM12872	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
46	CTCF	chr14:22236460-22236610	HEEpiC	esophagus:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
47	CTCF	chr14:22236466-22236732	K562	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
48	CTCF	chr14:22236460-22236610	GM12871	blood:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
49	CTCF	chr14:22236344-22236769	H1-hESC	embryonic stem cell:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566
50	CTCF	chr14:22236448-22236653	A549	lung:	n/a	chr14:22236543-22236561 chr14:22236544-22236560 chr14:22236545-22236566

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22241537-22241587	GM12891	blood:	n/a
2	chr14:22236018-22236068	AoSMC	blood vessel:	n/a
3	chr14:22236598-22236648	CMK	blood:	n/a
4	chr14:22236018-22236068	Jurkat	blood:	n/a
5	chr14:22236018-22236068	HUVEC	blood vessel:	n/a
6	chr14:22241537-22241587	Hela-S3	cervix:	n/a
7	chr14:22236018-22236068	SK-N-MC	brain:	n/a
8	chr14:22236598-22236648	RPTEC	kidney:	n/a
9	chr14:22241537-22241587	SKMC	muscle:	n/a
10	chr14:22241537-22241587	HAEpiC	amniotic membrane:	n/a
11	chr14:22236519-22236569	PFSK-1	brain:	n/a
12	chr14:22236018-22236068	K562	blood:	n/a
13	chr14:22236598-22236648	HAEpiC	amniotic membrane:	n/a
14	chr14:22241537-22241587	NHDF-neo	bronchial:	n/a
15	chr14:22241537-22241587	HEEpiC	esophagus:	n/a
16	chr14:22236018-22236068	HAEpiC	amniotic membrane:	n/a
17	chr14:22236598-22236648	GM12892	blood:	n/a
18	chr14:22236598-22236648	SAEC	small airway:	n/a
19	chr14:22236018-22236068	BJ	skin:	n/a
20	chr14:22236018-22236068	CMK	blood:	n/a
21	chr14:22236598-22236648	HUVEC	blood vessel:	n/a
22	chr14:22236519-22236569	PANC-1	pancreas:	n/a
23	chr14:22236598-22236648	HMEC	breast:	n/a
24	chr14:22236018-22236068	SK-N-SH	brain:	n/a
25	chr14:22236018-22236068	LNCaP	prostate:	n/a
26	chr14:22236018-22236068	HIPEpiC	eye:	n/a
27	chr14:22241537-22241587	AG04449	skin:	fetal
28	chr14:22236018-22236068	SKMC	muscle:	n/a
29	chr14:22241537-22241587	AG04450	lung:	fetal
30	chr14:22236598-22236648	Jurkat	blood:	n/a
31	chr14:22236598-22236648	GM19239	blood:	n/a
32	chr14:22236598-22236648	HIPEpiC	eye:	n/a
33	chr14:22236018-22236068	NHBE	bronchial:	n/a
34	chr14:22241537-22241587	HRPEpiC	eye:	n/a
35	chr14:22236018-22236068	PANC-1	pancreas:	n/a
36	chr14:22236598-22236648	BJ	skin:	n/a
37	chr14:22241537-22241587	ProgFib	skin:	n/a
38	chr14:22236598-22236648	HRCEpiC	kidney:	n/a
39	chr14:22236598-22236648	HepG2	liver:	n/a
40	chr14:22236519-22236569	AG04449	skin:	fetal
41	chr14:22236519-22236569	BE2_C	brain:	n/a
42	chr14:22236018-22236068	AG09319	gingival:	n/a
43	chr14:22236598-22236648	NB4	blood:	n/a
44	chr14:22236598-22236648	HNPCEpiC	eye:	n/a
45	chr14:22241537-22241587	NB4	blood:	n/a
46	chr14:22236018-22236068	HepG2	liver:	n/a
47	chr14:22241537-22241587	NH-A	brain:	n/a
48	chr14:22236018-22236068	ovcar-3	ovarian:	n/a
49	chr14:22236598-22236648	K562	blood:	n/a
50	chr14:22236519-22236569	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:22238003..22239945-chr14:22252615..22254697,2	MCF-7	breast:
2	chr14:22236090..22236721-chr14:22293035..22293909,3	MCF-7	breast:
3	chr14:22238003..22239945-chr14:22252615..22254697,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AE000662.92.1-10	chr14:22237068-22237313	NONHSAT035705

Variant related genes	Relation type
TRAV7	TF binding region
TRAV6	TF binding region
ENSG00000222776	TF binding region
TRAV7	CpG island
TRAV6	CpG island
ENSG00000222776	CpG island
ENSG00000211784	chromatin interactions

Extended variants
information (count: 908 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12434054	chr14:22221211-22221212	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531849788	chr14:22221265-22221266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74035048	chr14:22221275-22221276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs568485174	chr14:22221316-22221317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534457844	chr14:22221344-22221345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184133636	chr14:22221424-22221425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532368548	chr14:22221456-22221457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73574260	chr14:22221462-22221463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs539643922	chr14:22221512-22221513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147321544	chr14:22221559-22221560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527531413	chr14:22221564-22221565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368214895	chr14:22221639-22221640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537552576	chr14:22221746-22221747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529934891	chr14:22221819-22221820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140743096	chr14:22221878-22221879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574110651	chr14:22221915-22221916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540250525	chr14:22221920-22221921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11621081	chr14:22222017-22222018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs577108815	chr14:22222046-22222047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567259239	chr14:22222086-22222087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562673304	chr14:22222113-22222114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144588070	chr14:22222128-22222129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113548214	chr14:22222158-22222159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189461943	chr14:22222174-22222175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527665393	chr14:22222205-22222206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547819358	chr14:22222247-22222248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571049760	chr14:22222293-22222294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540136905	chr14:22222302-22222303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531025355	chr14:22222303-22222304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140476394	chr14:22222317-22222318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113187005	chr14:22222350-22222351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11621221	chr14:22222384-22222385	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs371785831	chr14:22222390-22222391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528794881	chr14:22222470-22222471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193039713	chr14:22222477-22222478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553739305	chr14:22222487-22222488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577015801	chr14:22222495-22222496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144412948	chr14:22222496-22222497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546905114	chr14:22222521-22222522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576286384	chr14:22222546-22222547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568387458	chr14:22222554-22222555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542076754	chr14:22222561-22222562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553876681	chr14:22222565-22222566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572161350	chr14:22222566-22222567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562162746	chr14:22222567-22222568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527829271	chr14:22222568-22222569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112956354	chr14:22222576-22222577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115428667	chr14:22222677-22222678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551115890	chr14:22222679-22222680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533430463	chr14:22222710-22222711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21364760	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22219000-22228600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:22228600-22228800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:22228600-22229000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr14:22228600-22229200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr14:22228800-22229000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:22236200-22236800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr14:22236200-22237000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr14:22236200-22237400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr14:22236200-22237400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr14:22236400-22236600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr14:22236400-22237000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr14:22236600-22236800	Enhancers	Primary T cells fromperipheralblood	blood
13	chr14:22236600-22237000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:22236600-22237000	Active TSS	Thymus	Thymus
15	chr14:22236600-22237400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr14:22236800-22237000	Enhancers	Fetal Thymus	thymus
17	chr14:22236800-22237200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr14:22236800-22237200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
19	chr14:22236800-22237400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr14:22236800-22237400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr14:22237000-22244600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr14:22237400-22239600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr14:22237400-22245000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr14:22239400-22240200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr14:22239600-22240200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:22239600-22240400	Enhancers	HMEC	breast
27	chr14:22239600-22240400	Enhancers	NHEK	skin
28	chr14:22239800-22240200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr14:22239800-22240400	Enhancers	Placenta Amnion	Placenta Amnion
30	chr14:22240000-22244600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr14:22241400-22242000	Enhancers	HepG2	liver
32	chr14:22244400-22245400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr14:22244400-22245600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr14:22244600-22245400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr14:22244600-22245400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr14:22244800-22245600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr14:22245000-22245200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr14:22245200-22245800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:22245400-22248600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr14:22245400-22248600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr14:22245400-22248600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr14:22245800-22246200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr14:22246200-22246400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr14:22246400-22246800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr14:22248600-22248800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr14:22248600-22248800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
47	chr14:22248600-22248800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr14:22248600-22248800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr14:22248600-22249000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr14:22248800-22249000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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