Variant report

Variant	esv3341635
Chromosome Location	chr1:228466379-228469177
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	HMGN3	chr1:228467014-228467068	K562	blood:	n/a	n/a
2	HNF4A	chr1:228467144-228467520	HepG2	liver:	n/a	chr1:228467192-228467205 chr1:228467192-228467204 chr1:228467192-228467204 chr1:228467193-228467205 chr1:228467191-228467206 chr1:228467189-228467207 chr1:228467192-228467204
3	HNF4A	chr1:228467147-228467423	HepG2	liver:	n/a	chr1:228467192-228467205 chr1:228467192-228467204 chr1:228467192-228467204 chr1:228467193-228467205 chr1:228467191-228467206 chr1:228467189-228467207 chr1:228467192-228467204
4	HNF4A	chr1:228467133-228467519	HepG2	liver:	n/a	chr1:228467192-228467205 chr1:228467192-228467204 chr1:228467192-228467204 chr1:228467193-228467205 chr1:228467191-228467206 chr1:228467189-228467207 chr1:228467192-228467204
5	JUND	chr1:228468139-228468282	HepG2	liver:	n/a	chr1:228468148-228468155 chr1:228468145-228468156 chr1:228468147-228468156
6	POLR2A	chr1:228466702-228467117	K562	blood:	n/a	n/a
7	POLR2A	chr1:228466913-228466916	K562	blood:	n/a	n/a
8	POLR2A	chr1:228469110-228469415	K562	blood:	n/a	n/a
9	POLR2A	chr1:228467504-228467868	K562	blood:	n/a	n/a
10	POLR2A	chr1:228467267-228467474	K562	blood:	n/a	n/a
11	POLR2A	chr1:228467212-228467232	K562	blood:	n/a	n/a
12	RCOR1	chr1:228467219-228467220	HepG2	liver:	n/a	n/a
13	RXRA	chr1:228467170-228467463	HepG2	liver:	n/a	n/a
14	ZNF263	chr1:228467951-228468282	HEK293-T-REx	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228466523-228466573	NH-A	brain:	n/a
2	chr1:228466523-228466573	NH-A	brain:	n/a
3	chr1:228468399-228468449	HL-60	blood:	n/a
4	chr1:228466616-228466666	SK-N-SH_RA	brain:	n/a
5	chr1:228468624-228468674	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:228466789-228466839	H1-hESC	embryonic stem cell:	embryo
7	chr1:228466523-228466573	SK-N-SH	brain:	n/a
8	chr1:228468399-228468449	IMR90	lung:	fetal
9	chr1:228467995-228468045	NB4	blood:	n/a
10	chr1:228468281-228468331	GM06990	blood:	n/a
11	chr1:228467988-228468038	ovcar-3	ovarian:	n/a
12	chr1:228466971-228467021	AoSMC	blood vessel:	n/a
13	chr1:228466789-228466839	AG04449	skin:	fetal
14	chr1:228467995-228468045	U87	brain:	n/a
15	chr1:228468624-228468674	GM12891	blood:	n/a
16	chr1:228466523-228466573	MCF10A-Er-Src	breast:	n/a
17	chr1:228468399-228468449	BE2_C	brain:	n/a
18	chr1:228468624-228468674	HCPEpiC	choroid plexus:	n/a
19	chr1:228468624-228468674	GM19239	blood:	n/a
20	chr1:228466616-228466666	U87	brain:	n/a
21	chr1:228467988-228468038	HAEpiC	amniotic membrane:	n/a
22	chr1:228468399-228468449	LNCaP	prostate:	n/a
23	chr1:228466481-228466531	AG09309	skin:	n/a
24	chr1:228468281-228468331	Hela-S3	cervix:	n/a
25	chr1:228466789-228466839	HCM	heart:	n/a
26	chr1:228466481-228466531	NB4	blood:	n/a
27	chr1:228466971-228467021	SK-N-SH	brain:	n/a
28	chr1:228468281-228468331	ECC-1	luminal epithelium:	n/a
29	chr1:228467995-228468045	RPTEC	kidney:	n/a
30	chr1:228466523-228466573	HAEpiC	amniotic membrane:	n/a
31	chr1:228468624-228468674	AG09309	skin:	n/a
32	chr1:228466616-228466666	MCF10A-Er-Src	breast:	n/a
33	chr1:228467988-228468038	NT2-D1	testis:	n/a
34	chr1:228466481-228466531	H1-hESC	embryonic stem cell:	embryo
35	chr1:228466616-228466666	Hepatocyte	liver:	n/a
36	chr1:228468624-228468674	HRPEpiC	eye:	n/a
37	chr1:228466616-228466666	HRE	kidney:	n/a
38	chr1:228467995-228468045	NHBE	bronchial:	n/a
39	chr1:228467988-228468038	Caco-2	colon:	n/a
40	chr1:228467995-228468045	BE2_C	brain:	n/a
41	chr1:228466789-228466839	HNPCEpiC	eye:	n/a
42	chr1:228466616-228466666	BE2_C	brain:	n/a
43	chr1:228467995-228468045	ProgFib	skin:	n/a
44	chr1:228466616-228466666	SK-N-SH	brain:	n/a
45	chr1:228467995-228468045	AG09309	skin:	n/a
46	chr1:228466971-228467021	AG04450	lung:	fetal
47	chr1:228466523-228466573	Jurkat	blood:	n/a
48	chr1:228466789-228466839	HRPEpiC	eye:	n/a
49	chr1:228467988-228468038	HL-60	blood:	n/a
50	chr1:228468399-228468449	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:228461911..228467066-chr1:228644143..228647181,7	K562	blood:
2	chr1:228451031..228452706-chr1:228468801..228471254,2	K562	blood:
3	chr1:228326053..228331395-chr1:228462710..228467617,6	K562	blood:
4	chr1:228461911..228467066-chr1:228644125..228647181,7	K562	blood:
5	chr1:228463910..228466494-chr1:228485377..228488310,3	K562	blood:
6	chr1:228466929..228469506-chr1:228481575..228484301,2	MCF-7	breast:

Variant related genes	Relation type
OBSCN	TF binding region
ENSG00000269890	TF binding region
ENSG00000269934	TF binding region
OBSCN	CpG island
ENSG00000269890	CpG island
ENSG00000269934	CpG island
ENSG00000196890	chromatin interactions
ENSG00000143774	chromatin interactions
ENSG00000154358	chromatin interactions
ENSG00000181218	chromatin interactions

Extended variants
information (count: 217 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:217 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372842796	chr1:228466381-228466382	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs375626143	chr1:228466382-228466383	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs370223099	chr1:228466394-228466395	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs375460960	chr1:228466404-228466405	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs199507178	chr1:228466407-228466408	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs556474884	chr1:228466411-228466412	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs371160335	chr1:228466426-228466427	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs575123570	chr1:228466473-228466474	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs374417116	chr1:228466474-228466475	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs368289371	chr1:228466481-228466482	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs371888438	chr1:228466491-228466492	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs376880740	chr1:228466492-228466493	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs367606070	chr1:228466505-228466506	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs563978931	chr1:228466523-228466524	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs533059830	chr1:228466524-228466525	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs540397543	chr1:228466530-228466531	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs419175	chr1:228466559-228466560	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs368389773	chr1:228466560-228466561	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs371487293	chr1:228466571-228466572	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs376684253	chr1:228466586-228466587	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs370014164	chr1:228466595-228466596	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs373620357	chr1:228466600-228466601	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs375410104	chr1:228466612-228466613	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs369587737	chr1:228466619-228466620	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs528950822	chr1:228466620-228466621	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs148070926	chr1:228466628-228466629	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs569176475	chr1:228466650-228466651	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs376056036	chr1:228466681-228466682	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs370105619	chr1:228466697-228466698	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs3795782	chr1:228466750-228466751	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs571615372	chr1:228466772-228466773	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs534322266	chr1:228466778-228466779	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs553875844	chr1:228466780-228466781	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs567507396	chr1:228466789-228466790	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs368265701	chr1:228466790-228466791	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs536490162	chr1:228466795-228466796	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs556436243	chr1:228466797-228466798	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs115119380	chr1:228466819-228466820	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs116738258	chr1:228466820-228466821	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs372702062	chr1:228466831-228466832	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs377494197	chr1:228466842-228466843	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs142671595	chr1:228466843-228466844	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs200479271	chr1:228466850-228466851	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs374415752	chr1:228466852-228466853	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs576766508	chr1:228466856-228466857	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs540311240	chr1:228466857-228466858	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs3820627	chr1:228466862-228466863	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs368201148	chr1:228466864-228466865	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs371033495	chr1:228466868-228466869	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs542843632	chr1:228466880-228466881	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Endometrioid adenocarcinoma	16974079	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
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228455400-228484800	Weak transcription	A549	lung
2	chr1:228456400-228485800	Weak transcription	Hela-S3	cervix
3	chr1:228457200-228472000	Weak transcription	Fetal Heart	heart
4	chr1:228459800-228469600	Weak transcription	HSMMtube	muscle
5	chr1:228463800-228481400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:228464000-228472200	Weak transcription	Small Intestine	intestine
7	chr1:228464200-228466400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr1:228464200-228470400	Weak transcription	HMEC	breast
9	chr1:228464200-228470600	Weak transcription	Aorta	Aorta
10	chr1:228464200-228473800	Weak transcription	Psoas Muscle	Psoas
11	chr1:228464200-228473800	Weak transcription	NHEK	skin
12	chr1:228464200-228478000	Strong transcription	Dnd41	blood
13	chr1:228464200-228491600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr1:228464400-228466400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr1:228464400-228466400	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr1:228464400-228467000	Weak transcription	Brain Cingulate Gyrus	brain
17	chr1:228464400-228467600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:228464400-228468000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr1:228464400-228468400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr1:228464400-228469200	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr1:228464400-228470600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr1:228464400-228470600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr1:228464400-228471800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:228464400-228472000	Genic enhancers	Skeletal Muscle Female	skeletal muscle
25	chr1:228464400-228473000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr1:228464400-228478400	Strong transcription	Thymus	Thymus
27	chr1:228464400-228479600	Weak transcription	Right Atrium	heart
28	chr1:228464400-228481400	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr1:228464400-228482000	Weak transcription	Fetal Kidney	kidney
30	chr1:228464400-228489200	Strong transcription	Left Ventricle	heart
31	chr1:228464600-228466600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr1:228464600-228466600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:228464600-228467200	Weak transcription	Duodenum Mucosa	Duodenum
34	chr1:228464600-228467400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
35	chr1:228464600-228467800	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr1:228464600-228467800	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr1:228464600-228468400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:228464600-228468800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr1:228464600-228470800	Weak transcription	Adipose Nuclei	Adipose
40	chr1:228464600-228473600	Weak transcription	Primary B cells from cord blood	blood
41	chr1:228464600-228475400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:228464600-228476800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:228464600-228481400	Weak transcription	Primary hematopoietic stem cells	blood
44	chr1:228464600-228483200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr1:228464600-228483200	Strong transcription	Fetal Intestine Small	intestine
46	chr1:228464600-228487000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr1:228464800-228466400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr1:228464800-228466400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr1:228464800-228466600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:228464800-228466800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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