Variant report

Variant	nsv535352
Chromosome Location	chr1:238188117-238574960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1459)
CpG islands
(count:305)
Chromatin interactive
region (count:20)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1459 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:238415600-238415834	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:238509171-238509547	HepG2	liver:	n/a	n/a
3	ATF1	chr1:238256429-238256482	K562	blood:	n/a	n/a
4	ATF1	chr1:238291470-238291619	K562	blood:	n/a	n/a
5	ATF1	chr1:238236482-238236623	K562	blood:	n/a	n/a
6	ATF1	chr1:238337127-238337233	K562	blood:	n/a	n/a
7	ATF2	chr1:238404899-238405298	GM12878	blood:	n/a	n/a
8	ATF2	chr1:238404955-238405231	GM12878	blood:	n/a	n/a
9	ATF2	chr1:238350498-238351209	GM12878	blood:	n/a	n/a
10	ATF2	chr1:238415615-238416037	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:238382619-238382748	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:238418308-238418677	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr1:238350488-238351096	GM12878	blood:	n/a	n/a
14	BATF	chr1:238226773-238227108	GM12878	blood:	n/a	chr1:238226950-238226960 chr1:238226949-238226960
15	BATF	chr1:238504382-238504631	GM12878	blood:	n/a	chr1:238504431-238504440 chr1:238504503-238504514 chr1:238504504-238504514 chr1:238504508-238504518
16	BATF	chr1:238362384-238362544	GM12878	blood:	n/a	n/a
17	BATF	chr1:238225506-238225892	GM12878	blood:	n/a	chr1:238225735-238225746
18	BATF	chr1:238225610-238225861	GM12878	blood:	n/a	chr1:238225735-238225746
19	BATF	chr1:238404830-238405291	GM12878	blood:	n/a	chr1:238405061-238405072
20	BATF	chr1:238386578-238386825	GM12878	blood:	n/a	chr1:238386730-238386741
21	BATF	chr1:238402640-238402935	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:238225481-238225876	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:238223441-238223672	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:238317302-238317549	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:238386648-238386894	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:238404807-238405328	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:238402612-238403059	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:238350484-238350874	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:238350471-238351213	GM12878	blood:	n/a	n/a
30	BCL3	chr1:238404959-238405191	GM12878	blood:	n/a	n/a
31	BCLAF1	chr1:238404974-238405204	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:238306489-238306640	GM12878	blood:	n/a	chr1:238306500-238306509 chr1:238306499-238306508 chr1:238306499-238306508 chr1:238306497-238306510 chr1:238306493-238306514
33	BHLHE40	chr1:238306486-238306677	K562	blood:	n/a	chr1:238306500-238306509 chr1:238306499-238306508 chr1:238306499-238306508 chr1:238306497-238306510 chr1:238306493-238306514
34	BHLHE40	chr1:238350542-238351079	GM12878	blood:	n/a	n/a
35	BHLHE40	chr1:238225228-238225834	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:238223413-238223753	GM12878	blood:	n/a	n/a
37	BRCA1	chr1:238476183-238476253	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr1:238511858-238511895	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr1:238415663-238415946	H1-hESC	embryonic stem cell:	n/a	n/a
40	CBX3	chr1:238402069-238402312	K562	blood:	n/a	n/a
41	CEBPB	chr1:238494889-238495170	K562	blood:	n/a	chr1:238495053-238495064
42	CEBPB	chr1:238396414-238396659	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:238494902-238495225	IMR90	lung:	n/a	chr1:238495053-238495064
44	CEBPB	chr1:238411798-238411978	A549	lung:	n/a	chr1:238411901-238411914 chr1:238411845-238411854 chr1:238411845-238411856
45	CEBPB	chr1:238338612-238338859	HepG2	liver:	n/a	chr1:238338795-238338806
46	CEBPB	chr1:238349168-238349440	A549	lung:	n/a	chr1:238349284-238349293 chr1:238349284-238349295 chr1:238349186-238349203 chr1:238349282-238349293 chr1:238349282-238349295 chr1:238349282-238349295
47	CEBPB	chr1:238559442-238559698	Hela-S3	cervix:	n/a	chr1:238559551-238559564 chr1:238559551-238559564 chr1:238559551-238559564 chr1:238559553-238559564 chr1:238559551-238559562 chr1:238559553-238559562
48	CEBPB	chr1:238486692-238487151	A549	lung:	n/a	chr1:238486969-238486980 chr1:238486968-238486981 chr1:238486970-238486979 chr1:238486970-238486979 chr1:238486970-238486979
49	CEBPB	chr1:238237026-238237285	K562	blood:	n/a	n/a
50	CEBPB	chr1:238568159-238568398	HepG2	liver:	n/a	chr1:238568324-238568335

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:238226289-238226339	NHBE	bronchial:	n/a
2	chr1:238417847-238417897	Caco-2	colon:	n/a
3	chr1:238490308-238490358	HMEC	breast:	n/a
4	chr1:238341559-238341609	SKMC	muscle:	n/a
5	chr1:238341559-238341609	A549	lung:	n/a
6	chr1:238341559-238341609	HRCEpiC	kidney:	n/a
7	chr1:238540640-238540690	NT2-D1	testis:	n/a
8	chr1:238226289-238226339	NHDF-neo	bronchial:	n/a
9	chr1:238226289-238226339	ECC-1	luminal epithelium:	n/a
10	chr1:238226289-238226339	ovcar-3	ovarian:	n/a
11	chr1:238226289-238226339	GM12892	blood:	n/a
12	chr1:238226289-238226339	HL-60	blood:	n/a
13	chr1:238490308-238490358	AG09309	skin:	n/a
14	chr1:238540640-238540690	Jurkat	blood:	n/a
15	chr1:238490308-238490358	CMK	blood:	n/a
16	chr1:238341559-238341609	GM12891	blood:	n/a
17	chr1:238226289-238226339	HIPEpiC	eye:	n/a
18	chr1:238540640-238540690	SK-N-SH_RA	brain:	n/a
19	chr1:238417847-238417897	H1-hESC	embryonic stem cell:	embryo
20	chr1:238490308-238490358	HNPCEpiC	eye:	n/a
21	chr1:238417847-238417897	AG09309	skin:	n/a
22	chr1:238490308-238490358	GM19239	blood:	n/a
23	chr1:238417847-238417897	U87	brain:	n/a
24	chr1:238540640-238540690	BJ	skin:	n/a
25	chr1:238417847-238417897	GM06990	blood:	n/a
26	chr1:238540640-238540690	SKMC	muscle:	n/a
27	chr1:238417847-238417897	HRCEpiC	kidney:	n/a
28	chr1:238226289-238226339	GM06990	blood:	n/a
29	chr1:238490308-238490358	ovcar-3	ovarian:	n/a
30	chr1:238341559-238341609	BE2_C	brain:	n/a
31	chr1:238341559-238341609	Caco-2	colon:	n/a
32	chr1:238540640-238540690	Hepatocyte	liver:	n/a
33	chr1:238417847-238417897	T-47D	breast:	n/a
34	chr1:238540640-238540690	NHBE	bronchial:	n/a
35	chr1:238417847-238417897	NB4	blood:	n/a
36	chr1:238490308-238490358	HUVEC	blood vessel:	n/a
37	chr1:238341559-238341609	LNCaP	prostate:	n/a
38	chr1:238540640-238540690	GM12878	blood:	n/a
39	chr1:238417847-238417897	HPAEpiC	pulmonary alveolar:	n/a
40	chr1:238540640-238540690	HRE	kidney:	n/a
41	chr1:238490308-238490358	Jurkat	blood:	n/a
42	chr1:238341559-238341609	CMK	blood:	n/a
43	chr1:238417847-238417897	GM12891	blood:	n/a
44	chr1:238341559-238341609	PrEC	prostate:	n/a
45	chr1:238341559-238341609	RPTEC	kidney:	n/a
46	chr1:238417847-238417897	HCT-116	colon:	n/a
47	chr1:238490308-238490358	Caco-2	colon:	n/a
48	chr1:238226289-238226339	MCF10A-Er-Src	breast:	n/a
49	chr1:238226289-238226339	H1-hESC	embryonic stem cell:	embryo
50	chr1:238540640-238540690	PFSK-1	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:238027519..238028172-chr1:238415271..238416018,2	MCF-7	breast:
2	chr1:238323741..238325866-chr1:238349570..238352017,2	MCF-7	breast:
3	chr1:238415665..238416312-chr1:239114796..239115754,2	MCF-7	breast:
4	chr1:238328791..238331678-chr1:238332085..238334237,2	K562	blood:
5	chr1:238457966..238460007-chr1:238462730..238464980,2	K562	blood:
6	chr1:238389177..238392116-chr1:238401287..238404252,2	K562	blood:
7	chr1:238323741..238325866-chr1:238349570..238352017,2	MCF-7	breast:
8	chr1:238328791..238331678-chr1:238332085..238334237,2	K562	blood:
9	chr1:238429285..238431857-chr1:238432645..238434405,2	K562	blood:
10	chr1:238401542..238402387-chr1:239114790..239115763,2	MCF-7	breast:
11	chr1:238252723..238255452-chr1:238273618..238275800,2	K562	blood:
12	chr1:238429285..238431857-chr1:238432645..238434405,2	K562	blood:
13	chr1:238493493..238495641-chr1:238497004..238499734,2	K562	blood:
14	chr1:238493493..238495641-chr1:238497004..238499734,2	K562	blood:
15	chr1:238389177..238392116-chr1:238401287..238404252,2	K562	blood:
16	chr1:238457966..238460007-chr1:238462730..238464980,2	K562	blood:
17	chr1:238569164..238571164-chr1:238574150..238576513,2	K562	blood:
18	chr1:238252723..238255452-chr1:238273618..238275800,2	K562	blood:
19	chr1:238569164..238571164-chr1:238574150..238576513,2	K562	blood:
20	chr1:238415693..238416233-chr1:238745605..238746502,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZP4-4	chr1:238271513-238271867	NONHSAT010452
2	lnc-RYR2-6	chr1:238486383-238486508	NONHSAT010457
3	lnc-RYR2-1	chr1:238439137-238439548	NONHSAT010455
4	lnc-RYR2-1	chr1:238439337-238439459	ENSG00000234464
5	lnc-RYR2-6	chr1:238535201-238535295	NONHSAT010457
6	lnc-ZP4-4	chr1:238271036-238271192	NONHSAT010452
7	lnc-RYR2-6	chr1:238489065-238489133	NONHSAT010457
8	lnc-RYR2-1	chr1:238450243-238450316	NONHSAT010455
9	lnc-RYR2-6	chr1:238489512-238489574	NONHSAT010457
10	lnc-RYR2-1	chr1:238450243-238450316	ENSG00000234464

No data

Variant related genes	Relation type
ENSG00000234464	TF binding region
ENSG00000232989	TF binding region
RNU6-725P	TF binding region
YWHAQP9	TF binding region
ENSG00000234464	CpG island
ENSG00000232989	CpG island
RNU6-725P	CpG island
YWHAQP9	CpG island

Extended variants
information (count: 10463 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:10463 , 50 per page) page: 1 2 3 4 5 6 7 ... 210

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570082173	chr1:238189658-238189659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537524762	chr1:238189708-238189709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184739301	chr1:238189729-238189730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374011865	chr1:238189748-238189749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574135255	chr1:238189853-238189854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541303216	chr1:238189872-238189873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553245976	chr1:238189875-238189876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577943646	chr1:238189888-238189889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189049719	chr1:238189916-238189917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539768005	chr1:238189969-238189970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114904352	chr1:238189981-238189982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192989134	chr1:238189999-238190000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74820032	chr1:238190015-238190016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558050004	chr1:238190023-238190024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576142050	chr1:238190061-238190062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560862256	chr1:238190104-238190105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146530590	chr1:238190197-238190198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149105475	chr1:238190275-238190276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368989196	chr1:238190330-238190331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373462882	chr1:238190353-238190354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532414015	chr1:238190369-238190370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570066708	chr1:238190390-238190391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550915211	chr1:238190410-238190411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545910756	chr1:238190484-238190485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368686010	chr1:238190549-238190550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569985948	chr1:238190577-238190578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143168831	chr1:238190600-238190601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555820616	chr1:238190628-238190629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116933509	chr1:238190694-238190695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185231063	chr1:238190702-238190703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs151202141	chr1:238190734-238190735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12131724	chr1:238190736-238190737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577829860	chr1:238190767-238190768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545252692	chr1:238190816-238190817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34954671	chr1:238190888-238190889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189705965	chr1:238190945-238190946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147875102	chr1:238190956-238190957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs67830893	chr1:238190957-238190958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141603856	chr1:238190958-238190959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200913688	chr1:238190959-238190960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201581283	chr1:238190961-238190962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575169355	chr1:238190966-238190967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542306987	chr1:238190973-238190974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147315008	chr1:238190985-238190986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555211227	chr1:238191012-238191013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74149816	chr1:238191053-238191054	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs534976174	chr1:238191094-238191095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140252075	chr1:238191130-238191131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565045868	chr1:238191167-238191168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142977788	chr1:238191173-238191174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Tetralogy of Fallot	22912587	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:658 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:238189600-238191400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr1:238190000-238191200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr1:238190000-238191400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr1:238190000-238191400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr1:238190600-238190800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr1:238190600-238190800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:238190600-238191200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr1:238190600-238191200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr1:238190600-238191400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr1:238190800-238192400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:238191200-238192400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr1:238191400-238192400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr1:238191400-238192400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr1:238191400-238192400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr1:238192400-238192800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:238192400-238193000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr1:238192400-238193000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr1:238192400-238193000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr1:238192400-238193200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr1:238192400-238193400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:238192600-238193000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr1:238192600-238193200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr1:238193000-238193400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:238193000-238193600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:238211800-238212000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:238212400-238212600	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr1:238213600-238216800	Enhancers	NHEK	skin
28	chr1:238214000-238216600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:238214000-238216800	Enhancers	HMEC	breast
30	chr1:238214200-238214400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:238214200-238214400	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr1:238214200-238216800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:238214400-238215000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:238214800-238215200	Enhancers	Esophagus	oesophagus
35	chr1:238214800-238215200	Active TSS	Fetal Kidney	kidney
36	chr1:238215000-238216800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:238215400-238215600	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr1:238215600-238216400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:238215600-238216400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr1:238216000-238216400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr1:238216400-238216600	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr1:238216800-238217200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:238216800-238217400	Weak transcription	HMEC	breast
44	chr1:238217200-238217800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:238217200-238217800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:238217800-238220800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr1:238220000-238220400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:238220800-238222000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:238221800-238222400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr1:238222000-238224600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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