Variant report

Variant	esv2830244
Chromosome Location	chr14:19035752-19461500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1539)
CpG islands
(count:611)
Chromatin interactive
region (count:0)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1539 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:19108228-19108420	K562	blood:	n/a	n/a
2	ATF1	chr14:19038969-19039342	K562	blood:	n/a	n/a
3	ATF1	chr14:19100486-19100700	K562	blood:	n/a	n/a
4	ATF1	chr14:19044418-19044791	K562	blood:	n/a	n/a
5	ATF1	chr14:19103184-19103383	K562	blood:	n/a	n/a
6	ATF1	chr14:19036176-19037332	K562	blood:	n/a	n/a
7	ATF1	chr14:19038248-19038629	K562	blood:	n/a	n/a
8	ATF1	chr14:19040731-19040981	K562	blood:	n/a	n/a
9	ATF1	chr14:19461425-19461537	K562	blood:	n/a	n/a
10	ATF1	chr14:19450073-19450214	K562	blood:	n/a	n/a
11	ATF1	chr14:19436953-19437483	K562	blood:	n/a	n/a
12	BACH1	chr14:19036232-19038897	K562	blood:	n/a	n/a
13	BACH1	chr14:19438368-19438886	K562	blood:	n/a	n/a
14	BACH1	chr14:19041796-19042864	K562	blood:	n/a	n/a
15	BATF	chr14:19038075-19038905	GM12878	blood:	n/a	n/a
16	BATF	chr14:19044988-19045347	GM12878	blood:	n/a	n/a
17	BATF	chr14:19135762-19136474	GM12878	blood:	n/a	n/a
18	BATF	chr14:19136515-19136845	GM12878	blood:	n/a	n/a
19	BATF	chr14:19038231-19038806	GM12878	blood:	n/a	n/a
20	BATF	chr14:19044473-19044720	GM12878	blood:	n/a	n/a
21	BATF	chr14:19183485-19183643	GM12878	blood:	n/a	chr14:19183575-19183586
22	BATF	chr14:19048060-19048470	GM12878	blood:	n/a	n/a
23	BATF	chr14:19040662-19040959	GM12878	blood:	n/a	n/a
24	BATF	chr14:19044389-19044783	GM12878	blood:	n/a	n/a
25	BATF	chr14:19054267-19054454	GM12878	blood:	n/a	n/a
26	BATF	chr14:19048063-19048406	GM12878	blood:	n/a	n/a
27	BATF	chr14:19068287-19068696	GM12878	blood:	n/a	n/a
28	BATF	chr14:19135407-19135704	GM12878	blood:	n/a	n/a
29	BATF	chr14:19036413-19036733	GM12878	blood:	n/a	n/a
30	BATF	chr14:19123750-19124046	GM12878	blood:	n/a	n/a
31	BATF	chr14:19047189-19047418	GM12878	blood:	n/a	n/a
32	BATF	chr14:19135459-19135699	GM12878	blood:	n/a	n/a
33	BATF	chr14:19183487-19183665	GM12878	blood:	n/a	chr14:19183575-19183586
34	BATF	chr14:19135785-19136194	GM12878	blood:	n/a	n/a
35	BATF	chr14:19092736-19092938	GM12878	blood:	n/a	n/a
36	BATF	chr14:19041961-19042330	GM12878	blood:	n/a	n/a
37	BATF	chr14:19041961-19042717	GM12878	blood:	n/a	n/a
38	BATF	chr14:19068281-19068796	GM12878	blood:	n/a	n/a
39	BCL11A	chr14:19041506-19041796	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:19038044-19038913	GM12878	blood:	n/a	n/a
41	BCL11A	chr14:19048070-19048424	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:19047142-19047425	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:19047122-19047351	GM12878	blood:	n/a	n/a
44	BCL11A	chr14:19068266-19068776	GM12878	blood:	n/a	n/a
45	BCL11A	chr14:19042068-19042440	GM12878	blood:	n/a	n/a
46	BCL11A	chr14:19074338-19074669	GM12878	blood:	n/a	n/a
47	BCL11A	chr14:19044525-19044699	GM12878	blood:	n/a	n/a
48	BCL11A	chr14:19036249-19036742	GM12878	blood:	n/a	n/a
49	BCL11A	chr14:19044398-19044718	GM12878	blood:	n/a	n/a
50	BCL11A	chr14:19038086-19038906	GM12878	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:19377109-19377159	SK-N-MC	brain:	n/a
2	chr14:19377109-19377159	SK-N-MC	brain:	n/a
3	chr14:19422337-19422387	HCPEpiC	choroid plexus:	n/a
4	chr14:19109438-19109488	PANC-1	pancreas:	n/a
5	chr14:19360878-19360928	HCPEpiC	choroid plexus:	n/a
6	chr14:19109768-19109818	ProgFib	skin:	n/a
7	chr14:19421688-19421738	LNCaP	prostate:	n/a
8	chr14:19109438-19109488	NB4	blood:	n/a
9	chr14:19360467-19360517	HNPCEpiC	eye:	n/a
10	chr14:19377109-19377159	GM12892	blood:	n/a
11	chr14:19360878-19360928	HMEC	breast:	n/a
12	chr14:19110297-19110347	HUVEC	blood vessel:	n/a
13	chr14:19413192-19413242	RPTEC	kidney:	n/a
14	chr14:19109768-19109818	H1-hESC	embryonic stem cell:	embryo
15	chr14:19109768-19109818	SK-N-MC	brain:	n/a
16	chr14:19402845-19402895	HUVEC	blood vessel:	n/a
17	chr14:19377109-19377159	AG04449	skin:	fetal
18	chr14:19402845-19402895	PFSK-1	brain:	n/a
19	chr14:19360878-19360928	HEK293	kidney:	embryo
20	chr14:19421688-19421738	K562	blood:	n/a
21	chr14:19360467-19360517	T-47D	breast:	n/a
22	chr14:19109438-19109488	NH-A	brain:	n/a
23	chr14:19109438-19109488	BJ	skin:	n/a
24	chr14:19360467-19360517	SKMC	muscle:	n/a
25	chr14:19110297-19110347	H1-hESC	embryonic stem cell:	embryo
26	chr14:19377109-19377159	MCF-7	breast:	n/a
27	chr14:19402845-19402895	HepG2	liver:	n/a
28	chr14:19110297-19110347	GM12878	blood:	n/a
29	chr14:19109768-19109818	SK-N-SH	brain:	n/a
30	chr14:19421688-19421738	GM19239	blood:	n/a
31	chr14:19422337-19422387	AG09309	skin:	n/a
32	chr14:19110297-19110347	SKMC	muscle:	n/a
33	chr14:19421688-19421738	NHBE	bronchial:	n/a
34	chr14:19422337-19422387	PFSK-1	brain:	n/a
35	chr14:19360878-19360928	Caco-2	colon:	n/a
36	chr14:19402845-19402895	Hepatocyte	liver:	n/a
37	chr14:19402845-19402895	HIPEpiC	eye:	n/a
38	chr14:19377109-19377159	AG09309	skin:	n/a
39	chr14:19422337-19422387	LNCaP	prostate:	n/a
40	chr14:19360878-19360928	RPTEC	kidney:	n/a
41	chr14:19110297-19110347	ProgFib	skin:	n/a
42	chr14:19377109-19377159	HRCEpiC	kidney:	n/a
43	chr14:19110297-19110347	AG09319	gingival:	n/a
44	chr14:19421688-19421738	HRPEpiC	eye:	n/a
45	chr14:19360467-19360517	HepG2	liver:	n/a
46	chr14:19421688-19421738	HAEpiC	amniotic membrane:	n/a
47	chr14:19413192-19413242	HRCEpiC	kidney:	n/a
48	chr14:19421688-19421738	GM06990	blood:	n/a
49	chr14:19109438-19109488	HCF	heart:	n/a
50	chr14:19402845-19402895	T-47D	breast:	n/a

No data

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEM-15	chr14:19459200-19459267	NONHSAT035446
2	lnc-OR11H12.1-6	chr14:19118171-19118336	NONHSAT035431
3	lnc-OR11H12.1-2	chr14:19339405-19339552	NONHSAT035436
4	lnc-OR11H12.1-2	chr14:19345173-19345267	NONHSAT035436
5	lnc-POTEM-9	chr14:19407015-19408008	NR_046104
6	lnc-OR11H12.1-1	chr14:19413561-19413898	ENSG00000258364.1
7	lnc-POTEM-9	chr14:19406795-19408008	ENSG00000257504
8	lnc-POTEM-9	chr14:19409942-19410111	ENSG00000257504
9	lnc-OR11H12.1-6	chr14:19114720-19114893	NONHSAT035431
10	lnc-POTEM-9	chr14:19409573-19409681	NR_046104
11	lnc-POTEM-10	chr14:19372736-19372787	ENSG00000257959.1
12	lnc-POTEM-9	chr14:19409573-19409681	ENSG00000257504
13	lnc-POTEM-9	chr14:19409942-19410111	NR_046104
14	lnc-POTEM-15	chr14:19458358-19458713	NONHSAT035446
15	lnc-OR11H12.1-6	chr14:19114450-19114555	NONHSAT035431
16	lnc-OR11H12.1-5	chr14:19195252-19195750	NONHSAT035433
17	lnc-OR11H12.1-2	chr14:19340299-19340388	NONHSAT035436
18	lnc-OR11H12.1-1	chr14:19412520-19412744	ENSG00000258364.1
19	lnc-OR11H12.1-2	chr14:19341921-19341993	NONHSAT035436
20	lnc-OR11H12.1-6	chr14:19110203-19110377	NONHSAT035431
21	lnc-POTEM-10	chr14:19332154-19332599	ENSG00000257959.1
22	lnc-OR11H12.1-6	chr14:19117091-19117203	NONHSAT035431

No data

Variant related genes	Relation type
ENSG00000257825	TF binding region
ENSG00000257959	TF binding region
ENSG00000258076	TF binding region
ENSG00000257558	TF binding region
ENSG00000238442	TF binding region
ENSG00000258364	TF binding region
ENSG00000257504	TF binding region
ENSG00000257175	TF binding region
ENSG00000257672	TF binding region
ENSG00000215398	TF binding region
ARHGAP42P5	TF binding region
RNU6-458P	TF binding region
ENSG00000257731	TF binding region
ENSG00000257171	TF binding region
ENSG00000258367	TF binding region
ENSG00000257356	TF binding region
ENSG00000257721	TF binding region
ENSG00000257644	TF binding region
OR11H12	TF binding region
ENSG00000257825	CpG island
ENSG00000257959	CpG island
ENSG00000258076	CpG island
ENSG00000257558	CpG island
ENSG00000238442	CpG island
ENSG00000258364	CpG island
ENSG00000257504	CpG island
ENSG00000257175	CpG island
ENSG00000257672	CpG island
ENSG00000215398	CpG island
ARHGAP42P5	CpG island
RNU6-458P	CpG island
ENSG00000257731	CpG island
ENSG00000257171	CpG island
ENSG00000258367	CpG island
ENSG00000257356	CpG island
ENSG00000257721	CpG island
ENSG00000257644	CpG island
OR11H12	CpG island

Extended variants
information (count: 4272 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4272 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28833015	chr14:19035752-19035753	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs369962102	chr14:19035757-19035758	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs555646209	chr14:19035764-19035765	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs201758625	chr14:19035770-19035771	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs199940945	chr14:19035772-19035773	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs200507816	chr14:19035774-19035775	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs574161582	chr14:19035785-19035786	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs145429433	chr14:19035799-19035800	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs187570810	chr14:19035803-19035804	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs534446750	chr14:19035823-19035824	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs137955847	chr14:19035837-19035838	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs113666007	chr14:19035843-19035844	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs372761129	chr14:19035844-19035845	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs577258017	chr14:19035846-19035847	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs544561526	chr14:19035852-19035853	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs556837769	chr14:19035860-19035861	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs575165546	chr14:19035871-19035872	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs146548420	chr14:19035878-19035879	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs542500261	chr14:19035886-19035887	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs201075519	chr14:19035894-19035895	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs202167177	chr14:19035897-19035898	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs560956322	chr14:19035902-19035903	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs149569217	chr14:19035914-19035915	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs370257434	chr14:19035920-19035921	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs190649816	chr14:19035923-19035924	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs199805523	chr14:19035926-19035927	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs376021218	chr14:19035927-19035928	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs370600591	chr14:19035929-19035930	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs528288192	chr14:19035940-19035941	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs541208363	chr14:19035948-19035949	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs201007898	chr14:19035952-19035953	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs559758987	chr14:19035959-19035960	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs201813535	chr14:19035963-19035964	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs533368904	chr14:19035964-19035965	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs111335001	chr14:19035973-19035974	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs201053587	chr14:19035980-19035981	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs202175075	chr14:19035984-19035985	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs146372358	chr14:19035985-19035986	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs200335425	chr14:19035992-19035993	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs112721102	chr14:19036018-19036019	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs139008541	chr14:19036021-19036022	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs112115488	chr14:19036025-19036026	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs113611888	chr14:19036034-19036035	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs28812507	chr14:19036041-19036042	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs148675248	chr14:19036073-19036074	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs146430480	chr14:19036084-19036085	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs201493211	chr14:19036089-19036090	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs544608649	chr14:19036092-19036093	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs138789952	chr14:19036099-19036100	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs199731233	chr14:19036103-19036104	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Lung cancer	18438408	CNVD
Schizophrenia	21399695	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
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	17640729	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
Schizophrenia	20967226	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20932292	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	17142309	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	20369283	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Incontinentia Pigmenti	22033527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	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
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ependymoma	20639864	CNVD
Williams Syndrome	20824207	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:19015000-19047800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr14:19026000-19049000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:19034400-19045200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr14:19034600-19047600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr14:19034800-19037200	ZNF genes & repeats	Liver	Liver
6	chr14:19034800-19037400	ZNF genes & repeats	HUVEC	blood vessel
7	chr14:19035000-19036000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr14:19035000-19039400	ZNF genes & repeats	Fetal Brain Male	brain
9	chr14:19035200-19037200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr14:19035200-19040000	ZNF genes & repeats	Primary T cells from cord blood	blood
11	chr14:19035200-19048000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
12	chr14:19036200-19038800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
13	chr14:19036200-19039400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:19036200-19042800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr14:19036400-19037000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
16	chr14:19037000-19037200	ZNF genes & repeats	GM12878-XiMat	blood
17	chr14:19037200-19038200	Weak transcription	GM12878-XiMat	blood
18	chr14:19037400-19038200	Weak transcription	HUVEC	blood vessel
19	chr14:19037800-19039400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
20	chr14:19038000-19038800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr14:19038000-19038800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
22	chr14:19038000-19040800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr14:19038000-19041400	ZNF genes & repeats	Liver	Liver
24	chr14:19038200-19038400	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr14:19038200-19038400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
26	chr14:19038200-19038400	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:19038200-19038400	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
28	chr14:19038200-19038400	ZNF genes & repeats	Right Ventricle	heart
29	chr14:19038200-19038400	ZNF genes & repeats	HSMM	muscle
30	chr14:19038200-19038400	ZNF genes & repeats	NHEK	skin
31	chr14:19038200-19038600	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr14:19038200-19038600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr14:19038200-19038600	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
34	chr14:19038200-19038600	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
35	chr14:19038200-19038600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
36	chr14:19038200-19038600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr14:19038200-19038600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
38	chr14:19038200-19038600	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
39	chr14:19038200-19038600	ZNF genes & repeats	Aorta	Aorta
40	chr14:19038200-19038600	ZNF genes & repeats	Brain Angular Gyrus	brain
41	chr14:19038200-19038600	ZNF genes & repeats	Brain Anterior Caudate	brain
42	chr14:19038200-19038600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
43	chr14:19038200-19038600	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
44	chr14:19038200-19038600	ZNF genes & repeats	Brain Substantia Nigra	brain
45	chr14:19038200-19038600	ZNF genes & repeats	Colonic Mucosa	Colon
46	chr14:19038200-19038600	ZNF genes & repeats	Colon Smooth Muscle	Colon
47	chr14:19038200-19038600	ZNF genes & repeats	Fetal Heart	heart
48	chr14:19038200-19038600	ZNF genes & repeats	Ovary	ovary
49	chr14:19038200-19038600	ZNF genes & repeats	Psoas Muscle	Psoas
50	chr14:19038200-19038600	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon

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