Variant report

Variant	esv3491346
Chromosome Location	chr1:246945629-246947627
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:64)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:64 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:246945245-246946092	K562	blood:	n/a	n/a
2	CEBPB	chr1:246945440-246945711	IMR90	lung:	n/a	n/a
3	CEBPB	chr1:246945459-246945696	HepG2	liver:	n/a	n/a
4	CTCF	chr1:246945920-246946070	AG04450	lung:	n/a	n/a
5	CTCF	chr1:246945860-246946010	HPF	lung:	n/a	n/a
6	CTCF	chr1:246946080-246946230	AG04450	lung:	n/a	n/a
7	CTCF	chr1:246945960-246946110	HBMEC	blood vessel:	n/a	n/a
8	CTCF	chr1:246945840-246945990	HMF	breast:	n/a	n/a
9	CTCF	chr1:246946060-246946210	HMF	breast:	n/a	n/a
10	CTCF	chr1:246945860-246946010	HPAF	blood vessel:	n/a	n/a
11	CTCF	chr1:246945980-246946130	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr1:246945920-246946070	GM12868	blood:	n/a	n/a
13	CTCF	chr1:246945905-246945966	GM19239	blood:	n/a	n/a
14	CTCF	chr1:246946060-246946210	HPAF	blood vessel:	n/a	n/a
15	E2F6	chr1:246945732-246946007	K562	blood:	n/a	n/a
16	FOSL2	chr1:246946102-246946919	HepG2	liver:	n/a	n/a
17	FOSL2	chr1:246946225-246946826	HepG2	liver:	n/a	n/a
18	FOXA1	chr1:246946300-246946837	HepG2	liver:	n/a	n/a
19	FOXP2	chr1:246945778-246946287	PFSK-1	brain:	n/a	n/a
20	GABPA	chr1:246946349-246946694	HepG2	liver:	n/a	n/a
21	GABPA	chr1:246946410-246946804	Hela-S3	cervix:	n/a	n/a
22	HEY1	chr1:246946372-246946755	K562	blood:	n/a	n/a
23	HEY1	chr1:246946228-246946847	HepG2	liver:	n/a	n/a
24	JUND	chr1:246946383-246946759	HepG2	liver:	n/a	n/a
25	JUND	chr1:246945443-246945712	K562	blood:	n/a	n/a
26	MAFF	chr1:246945458-246945663	K562	blood:	n/a	n/a
27	MAFF	chr1:246945637-246945641	HepG2	liver:	n/a	n/a
28	MAFK	chr1:246945981-246946121	HepG2	liver:	n/a	n/a
29	MAFK	chr1:246945991-246946060	HepG2	liver:	n/a	n/a
30	MAX	chr1:246945640-246945929	K562	blood:	n/a	n/a
31	MAX	chr1:246945430-246946342	NB4	blood:	n/a	n/a
32	MAX	chr1:246945972-246946272	K562	blood:	n/a	n/a
33	MAX	chr1:246947451-246948343	K562	blood:	n/a	chr1:246948130-246948140 chr1:246948123-246948139 chr1:246947801-246947808
34	MYC	chr1:246945439-246946283	NB4	blood:	n/a	n/a
35	NR3C1	chr1:246946178-246946880	A549	lung:	n/a	n/a
36	POLR2A	chr1:246945912-246946861	GM12878	blood:	n/a	n/a
37	POLR2A	chr1:246946132-246946837	GM12892	blood:	n/a	n/a
38	POLR2A	chr1:246945609-246945793	HepG2	liver:	n/a	n/a
39	POLR2A	chr1:246945333-246946193	U87	brain:	n/a	n/a
40	POLR2A	chr1:246946367-246946773	A549	lung:	n/a	n/a
41	POLR2A	chr1:246945328-246946442	HL-60	blood:	n/a	n/a
42	POLR2A	chr1:246945834-246946496	PANC-1	pancreas:	n/a	n/a
43	POLR2A	chr1:246945998-246946892	GM12891	blood:	n/a	n/a
44	POLR2A	chr1:246946262-246946746	HepG2	liver:	n/a	n/a
45	POLR2A	chr1:246947499-246947520	K562	blood:	n/a	n/a
46	POLR2A	chr1:246945253-246946164	U87	brain:	n/a	n/a
47	POLR2A	chr1:246946858-246946871	HepG2	liver:	n/a	n/a
48	POLR2A	chr1:246946908-246947023	HepG2	liver:	n/a	n/a
49	POLR2A	chr1:246946402-246946808	GM12892	blood:	n/a	n/a
50	POLR2A	chr1:246946882-246946898	HepG2	liver:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246947185..246952305-chr1:246952338..246955724,5	K562	blood:
2	chr1:246941244..246944008-chr1:246946969..246949951,3	MCF-7	breast:
3	chr1:246939030..246940776-chr1:246947263..246949787,2	MCF-7	breast:
4	chr1:246946643..246948588-chr1:247104112..247106785,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCCPDH-1	chr1:246947201-246947345	NONHSAT010738
2	lnc-SCCPDH-1	chr1:246947183-246947345	NONHSAT010737
3	lnc-SCCPDH-1	chr1:246946701-246947345	NONHSAT010736
4	lnc-SCCPDH-1	chr1:246947036-246947345	XLOC_000643

No data

Variant related genes	Relation type
KIF28P	TF binding region
ENSG00000227953	TF binding region
ENSG00000223519	chromatin interactions
ENSG00000227953	chromatin interactions

Extended variants
information (count: 132 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:132 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374267849	chr1:246945642-246945643	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548025285	chr1:246945648-246945649	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76815646	chr1:246945653-246945654	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148375041	chr1:246945654-246945655	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10624599	chr1:246945655-246945656	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs60107954	chr1:246945667-246945668	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs533316791	chr1:246945670-246945671	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536803690	chr1:246945672-246945673	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377309809	chr1:246945673-246945674	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185420834	chr1:246945742-246945743	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114333122	chr1:246945743-246945744	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150506035	chr1:246945751-246945752	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188435899	chr1:246945786-246945787	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78670245	chr1:246945793-246945794	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4244628	chr1:246945822-246945823	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs533802057	chr1:246945880-246945881	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs192856936	chr1:246945928-246945929	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs184177348	chr1:246945965-246945966	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs537213659	chr1:246946019-246946020	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs4926457	chr1:246946021-246946022	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs373962342	chr1:246946026-246946027	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs537736863	chr1:246946030-246946031	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs542756718	chr1:246946066-246946067	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs188117180	chr1:246946076-246946077	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs12410595	chr1:246946077-246946078	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs202005361	chr1:246946122-246946123	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs544696770	chr1:246946155-246946156	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs564773754	chr1:246946170-246946171	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs574293463	chr1:246946187-246946188	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs181013343	chr1:246946195-246946196	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs184897504	chr1:246946198-246946199	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs563580981	chr1:246946218-246946219	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541582283	chr1:246946219-246946220	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549411191	chr1:246946244-246946245	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12129256	chr1:246946260-246946261	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149745071	chr1:246946296-246946297	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61852514	chr1:246946314-246946315	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61852515	chr1:246946330-246946331	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190779999	chr1:246946352-246946353	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369962107	chr1:246946361-246946362	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200767816	chr1:246946371-246946372	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372237475	chr1:246946376-246946377	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35812304	chr1:246946377-246946378	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs57695616	chr1:246946381-246946382	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4926458	chr1:246946390-246946391	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528451684	chr1:246946394-246946395	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551504817	chr1:246946420-246946421	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369658231	chr1:246946434-246946435	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111419504	chr1:246946440-246946441	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112841668	chr1:246946446-246946447	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	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
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246888400-246946400	Weak transcription	Small Intestine	intestine
2	chr1:246902800-246952800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:246905000-246945800	Weak transcription	Psoas Muscle	Psoas
4	chr1:246921600-246945800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr1:246924400-246945800	Weak transcription	Primary B cells from cord blood	blood
6	chr1:246925200-246952200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:246932400-246945800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:246932400-246952000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr1:246932600-246948000	Strong transcription	Liver	Liver
10	chr1:246932600-246948600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:246932600-246948600	Weak transcription	Esophagus	oesophagus
12	chr1:246932800-246945800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr1:246932800-246948800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:246932800-246952400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr1:246932800-246956400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr1:246933200-246945800	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:246938400-246945800	Strong transcription	Fetal Stomach	stomach
18	chr1:246938400-246947200	Strong transcription	Fetal Intestine Small	intestine
19	chr1:246940200-246945800	Weak transcription	GM12878-XiMat	blood
20	chr1:246940200-246947600	Weak transcription	HUVEC	blood vessel
21	chr1:246940200-246948800	Weak transcription	Fetal Brain Male	brain
22	chr1:246940400-246945800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:246940400-246949000	Weak transcription	Rectal Smooth Muscle	rectum
24	chr1:246940600-246945800	Weak transcription	Primary T cells from cord blood	blood
25	chr1:246940600-246945800	Weak transcription	Ovary	ovary
26	chr1:246940600-246945800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr1:246940600-246948600	Weak transcription	Brain Angular Gyrus	brain
28	chr1:246940600-246948800	Weak transcription	Brain Cingulate Gyrus	brain
29	chr1:246940600-246948800	Weak transcription	Fetal Kidney	kidney
30	chr1:246940800-246945800	Weak transcription	Brain Hippocampus Middle	brain
31	chr1:246940800-246948000	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr1:246940800-246951600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr1:246940800-246951600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr1:246941200-246948200	Weak transcription	Duodenum Mucosa	Duodenum
35	chr1:246941200-246952600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:246941600-246948800	Weak transcription	Colonic Mucosa	Colon
37	chr1:246941600-246948800	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr1:246941600-246952200	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr1:246942200-246949000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr1:246942600-246945800	Weak transcription	Left Ventricle	heart
41	chr1:246942800-246952200	Weak transcription	Fetal Brain Female	brain
42	chr1:246943000-246945800	Weak transcription	Aorta	Aorta
43	chr1:246943000-246948000	Enhancers	Primary hematopoietic stem cells	blood
44	chr1:246943400-246945800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr1:246943400-246945800	Weak transcription	Spleen	Spleen
46	chr1:246943400-246952000	Weak transcription	Brain Anterior Caudate	brain
47	chr1:246944200-246945800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:246944200-246945800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr1:246944200-246947800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:246944400-246948800	Weak transcription	Gastric	stomach

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