Variant report

Variant	nsv510629
Chromosome Location	chr14:22134425-22215842
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	chr14:22179625-22179926	K562	blood:	n/a	n/a
2	ARID3A	chr14:22179625-22179949	HepG2	liver:	n/a	n/a
3	BACH1	chr14:22143914-22143985	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr14:22191831-22191884	HepG2	liver:	n/a	n/a
5	CEBPB	chr14:22179638-22180002	HepG2	liver:	n/a	chr14:22179946-22179959
6	CEBPB	chr14:22179110-22179134	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr14:22187935-22188129	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:22179643-22180005	K562	blood:	n/a	chr14:22179946-22179959
9	CEBPB	chr14:22179640-22179981	IMR90	lung:	n/a	chr14:22179946-22179959
10	CEBPB	chr14:22179639-22179945	A549	lung:	n/a	n/a
11	CEBPB	chr14:22179641-22179994	H1-hESC	embryonic stem cell:	n/a	chr14:22179946-22179959
12	CEBPB	chr14:22147887-22147981	H1-hESC	embryonic stem cell:	n/a	chr14:22147955-22147966
13	CEBPB	chr14:22171581-22171967	MCF-7	breast:	n/a	chr14:22171736-22171749
14	CEBPB	chr14:22162653-22162767	HepG2	liver:	n/a	chr14:22162686-22162697
15	CEBPB	chr14:22179540-22180055	MCF-7	breast:	n/a	chr14:22179946-22179959
16	CEBPB	chr14:22147801-22148121	HepG2	liver:	n/a	chr14:22147955-22147966
17	CEBPB	chr14:22179577-22179993	MCF-7	breast:	n/a	chr14:22179946-22179959
18	CEBPB	chr14:22162533-22162719	H1-hESC	embryonic stem cell:	n/a	chr14:22162686-22162697
19	CREB1	chr14:22191628-22192099	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr14:22191724-22192061	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr14:22202860-22203010	GM12865	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
22	CTCF	chr14:22191720-22191870	HAc	cerebellar:	n/a	chr14:22191842-22191860
23	CTCF	chr14:22202900-22203050	HRPEpiC	eye:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
24	CTCF	chr14:22179703-22179817	NHEK	skin:	n/a	chr14:22179774-22179795 chr14:22179773-22179789 chr14:22179772-22179790 chr14:22179775-22179788 chr14:22179775-22179788
25	CTCF	chr14:22179720-22179870	GM12868	blood:	n/a	chr14:22179774-22179795 chr14:22179773-22179789 chr14:22179772-22179790 chr14:22179775-22179788 chr14:22179775-22179788
26	CTCF	chr14:22191800-22191950	HCM	heart:	n/a	chr14:22191842-22191860
27	CTCF	chr14:22202813-22203061	LNCaP	prostate:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
28	CTCF	chr14:22179700-22179850	AG09319	gingival:	n/a	chr14:22179774-22179795 chr14:22179773-22179789 chr14:22179772-22179790 chr14:22179775-22179788 chr14:22179775-22179788
29	CTCF	chr14:22179360-22179510	HRE	kidney:	n/a	n/a
30	CTCF	chr14:22179680-22179830	GM12874	blood:	n/a	chr14:22179774-22179795 chr14:22179773-22179789 chr14:22179772-22179790 chr14:22179775-22179788 chr14:22179775-22179788
31	CTCF	chr14:22202880-22203030	GM12878	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
32	CTCF	chr14:22191780-22191930	HRPEpiC	eye:	n/a	chr14:22191842-22191860
33	CTCF	chr14:22179740-22179890	HMF	breast:	n/a	chr14:22179774-22179795 chr14:22179773-22179789 chr14:22179772-22179790 chr14:22179775-22179788 chr14:22179775-22179788
34	CTCF	chr14:22202795-22203078	K562	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
35	CTCF	chr14:22202861-22202988	Fibrobl	skin:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
36	CTCF	chr14:22202900-22203050	HUVEC	blood vessel:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
37	CTCF	chr14:22191760-22191910	GM12865	blood:	n/a	chr14:22191842-22191860
38	CTCF	chr14:22179720-22179870	GM12873	blood:	n/a	chr14:22179774-22179795 chr14:22179773-22179789 chr14:22179772-22179790 chr14:22179775-22179788 chr14:22179775-22179788
39	CTCF	chr14:22202880-22203030	HPAF	blood vessel:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
40	CTCF	chr14:22202918-22202963	GM19240	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
41	CTCF	chr14:22179680-22179830	GM12875	blood:	n/a	chr14:22179774-22179795 chr14:22179773-22179789 chr14:22179772-22179790 chr14:22179775-22179788 chr14:22179775-22179788
42	CTCF	chr14:22202840-22202990	K562	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
43	CTCF	chr14:22202820-22202970	AG10803	skin:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
44	CTCF	chr14:22191820-22191970	HUVEC	blood vessel:	n/a	chr14:22191842-22191860
45	CTCF	chr14:22191811-22191917	GM13976	blood:	n/a	chr14:22191842-22191860
46	CTCF	chr14:22179700-22179850	HCPEpiC	choroid plexus:	n/a	chr14:22179774-22179795 chr14:22179773-22179789 chr14:22179772-22179790 chr14:22179775-22179788 chr14:22179775-22179788
47	CTCF	chr14:22202820-22202970	GM12864	blood:	n/a	chr14:22202940-22202961 chr14:22202939-22202955 chr14:22202938-22202956
48	CTCF	chr14:22179600-22179750	NHLF	lung:	n/a	n/a
49	CTCF	chr14:22191710-22192014	MCF-7	breast:	n/a	chr14:22191842-22191860
50	CTCF	chr14:22180680-22180830	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22191382-22191432	NT2-D1	testis:	n/a
2	chr14:22191382-22191432	K562	blood:	n/a
3	chr14:22191382-22191432	HEEpiC	esophagus:	n/a
4	chr14:22191856-22191906	HRPEpiC	eye:	n/a
5	chr14:22191856-22191906	AG09319	gingival:	n/a
6	chr14:22191888-22191938	HRCEpiC	kidney:	n/a
7	chr14:22191888-22191938	HPAEpiC	pulmonary alveolar:	n/a
8	chr14:22191761-22191811	H1-hESC	embryonic stem cell:	embryo
9	chr14:22191827-22191877	Hela-S3	cervix:	n/a
10	chr14:22191827-22191877	AG09309	skin:	n/a
11	chr14:22191856-22191906	MCF-7	breast:	n/a
12	chr14:22191382-22191432	PrEC	prostate:	n/a
13	chr14:22191382-22191432	LNCaP	prostate:	n/a
14	chr14:22191382-22191432	GM19239	blood:	n/a
15	chr14:22191888-22191938	NH-A	brain:	n/a
16	chr14:22191856-22191906	T-47D	breast:	n/a
17	chr14:22191856-22191906	ProgFib	skin:	n/a
18	chr14:22191382-22191432	SAEC	small airway:	n/a
19	chr14:22191827-22191877	HepG2	liver:	n/a
20	chr14:22191382-22191432	GM12892	blood:	n/a
21	chr14:22191827-22191877	HCT-116	colon:	n/a
22	chr14:22191382-22191432	HEK293	kidney:	embryo
23	chr14:22191761-22191811	HCPEpiC	choroid plexus:	n/a
24	chr14:22191888-22191938	SK-N-MC	brain:	n/a
25	chr14:22191856-22191906	PFSK-1	brain:	n/a
26	chr14:22191761-22191811	GM12878	blood:	n/a
27	chr14:22191888-22191938	Hela-S3	cervix:	n/a
28	chr14:22191888-22191938	HL-60	blood:	n/a
29	chr14:22191856-22191906	AG10803	skin:	n/a
30	chr14:22191827-22191877	ovcar-3	ovarian:	n/a
31	chr14:22191856-22191906	HCM	heart:	n/a
32	chr14:22191827-22191877	Hepatocyte	liver:	n/a
33	chr14:22191761-22191811	ECC-1	luminal epithelium:	n/a
34	chr14:22191888-22191938	HNPCEpiC	eye:	n/a
35	chr14:22191382-22191432	SK-N-SH	brain:	n/a
36	chr14:22191856-22191906	SK-N-SH	brain:	n/a
37	chr14:22191761-22191811	BE2_C	brain:	n/a
38	chr14:22191827-22191877	PrEC	prostate:	n/a
39	chr14:22191856-22191906	K562	blood:	n/a
40	chr14:22191856-22191906	HPAEpiC	pulmonary alveolar:	n/a
41	chr14:22191827-22191877	SK-N-MC	brain:	n/a
42	chr14:22191856-22191906	PANC-1	pancreas:	n/a
43	chr14:22191888-22191938	SAEC	small airway:	n/a
44	chr14:22191382-22191432	HPAEpiC	pulmonary alveolar:	n/a
45	chr14:22191856-22191906	AoSMC	blood vessel:	n/a
46	chr14:22191856-22191906	HRCEpiC	kidney:	n/a
47	chr14:22191856-22191906	HCT-116	colon:	n/a
48	chr14:22191382-22191432	HMEC	breast:	n/a
49	chr14:22191827-22191877	GM06990	blood:	n/a
50	chr14:22191761-22191811	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:22081094..22083875-chr14:22197364..22199332,2	MCF-7	breast:
2	chr14:22109038..22109779-chr14:22179252..22179808,3	MCF-7	breast:
3	chr14:22191619..22192367-chr14:22202463..22203027,2	MCF-7	breast:
4	chr14:22140885..22141748-chr5:66767836..66768488,2	MCF-7	breast:
5	chr14:22179693..22180223-chr14:22202227..22202999,2	MCF-7	breast:
6	chr14:22179693..22180223-chr14:22202227..22202999,2	MCF-7	breast:
7	chr14:22202912..22203435-chr14:22216852..22217387,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR10G2-1	chr14:22184112-22184486	ENSG00000248358
2	lnc-OR10G2-1	chr14:22183018-22183212	ENSG00000248358

Variant related genes	Relation type
RPL4P1	TF binding region
TRAV3	TF binding region
TRAV2	TF binding region
TRAV4	TF binding region
TRAV5	TF binding region
ENSG00000248358	TF binding region
ENSG00000256350	TF binding region
OR4E1	TF binding region
RPL4P1	CpG island
TRAV3	CpG island
TRAV2	CpG island
TRAV4	CpG island
TRAV5	CpG island
ENSG00000248358	CpG island
ENSG00000256350	CpG island
OR4E1	CpG island
ENSG00000211777	chromatin interactions

Extended variants
information (count: 2035 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2035 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146925686	chr14:22135000-22135001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571838756	chr14:22135039-22135040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148028265	chr14:22135071-22135072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148013729	chr14:22135107-22135108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188839203	chr14:22135120-22135121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543925568	chr14:22135166-22135167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370160159	chr14:22135172-22135173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140760295	chr14:22135175-22135176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574386756	chr14:22135188-22135189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17108975	chr14:22135269-22135270	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs182053351	chr14:22135315-22135316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377506183	chr14:22135321-22135322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13329051	chr14:22135336-22135337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs17108979	chr14:22135352-22135353	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs186923343	chr14:22135389-22135390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531804534	chr14:22135397-22135398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548709934	chr14:22135424-22135425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189767228	chr14:22135428-22135429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150459084	chr14:22135440-22135441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7149624	chr14:22135508-22135509	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs13379393	chr14:22135515-22135516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571111709	chr14:22135534-22135535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181461156	chr14:22135579-22135580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557087838	chr14:22135611-22135612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556311831	chr14:22135636-22135637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185281075	chr14:22135680-22135681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374524434	chr14:22135723-22135724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368372129	chr14:22135743-22135744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559701786	chr14:22135745-22135746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554654591	chr14:22135746-22135747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574496456	chr14:22135749-22135750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376482732	chr14:22135863-22135864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527411791	chr14:22135876-22135877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138247948	chr14:22135887-22135888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149614564	chr14:22135896-22135897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189885024	chr14:22135932-22135933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575585156	chr14:22135968-22135969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562632235	chr14:22135979-22135980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183220181	chr14:22135982-22135983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186484628	chr14:22136122-22136123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12892066	chr14:22136149-22136150	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs564785849	chr14:22136169-22136170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543382830	chr14:22136177-22136178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145182560	chr14:22136180-22136181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114374936	chr14:22136220-22136221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs117557127	chr14:22136226-22136227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539710217	chr14:22136235-22136236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139005762	chr14:22136244-22136245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141981988	chr14:22136271-22136272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376841627	chr14:22136278-22136279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Breast cancer	21858162	CNVD
Autism	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22135000-22135200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:22135200-22140200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:22136200-22136400	Enhancers	NH-A	brain
4	chr14:22136200-22137400	Enhancers	HSMM	muscle
5	chr14:22136200-22137600	Enhancers	HUVEC	blood vessel
6	chr14:22137000-22137200	Enhancers	NH-A	brain
7	chr14:22137400-22138000	Enhancers	HepG2	liver
8	chr14:22137600-22140000	Weak transcription	HUVEC	blood vessel
9	chr14:22140000-22140800	Enhancers	HUVEC	blood vessel
10	chr14:22140200-22140400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:22148000-22148400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr14:22148000-22148400	Enhancers	HUVEC	blood vessel
13	chr14:22148000-22148800	Enhancers	HSMM	muscle
14	chr14:22154200-22154600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr14:22166000-22166200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:22166200-22168000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:22167000-22169000	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr14:22167600-22168400	Enhancers	Colonic Mucosa	Colon
19	chr14:22167600-22168600	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr14:22168000-22168200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr14:22168000-22168600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:22168600-22169800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr14:22169000-22171000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr14:22169800-22170000	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr14:22170000-22170400	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr14:22170400-22173600	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr14:22171000-22171400	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr14:22171400-22172400	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr14:22171800-22172800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr14:22171800-22172800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr14:22171800-22172800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr14:22171800-22173200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr14:22172000-22172600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr14:22172000-22172600	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr14:22172000-22173000	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr14:22172000-22173000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr14:22172000-22173000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr14:22172000-22173200	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr14:22172200-22172600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr14:22172200-22173600	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr14:22172400-22172800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr14:22172400-22172800	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr14:22172600-22180600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr14:22174800-22175400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr14:22179400-22179600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
46	chr14:22179600-22179800	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr14:22180000-22180200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr14:22180200-22180400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
49	chr14:22180200-22180600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr14:22180400-22180600	Bivalent/Poised TSS	Thymus	Thymus

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