Variant report

Variant	nsv1003441
Chromosome Location	chr1:246491836-246537767
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:345)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246536567-246536576	K562	blood:	n/a	n/a
2	ARID3A	chr1:246514223-246514241	K562	blood:	n/a	n/a
3	ARID3A	chr1:246495436-246495765	K562	blood:	n/a	n/a
4	ATF1	chr1:246501515-246501774	K562	blood:	n/a	n/a
5	ATF1	chr1:246514087-246514345	K562	blood:	n/a	n/a
6	ATF1	chr1:246495450-246495686	K562	blood:	n/a	n/a
7	ATF1	chr1:246507966-246508030	K562	blood:	n/a	n/a
8	ATF2	chr1:246501723-246502313	GM12878	blood:	n/a	n/a
9	ATF2	chr1:246492949-246493723	GM12878	blood:	n/a	n/a
10	ATF2	chr1:246493100-246493631	GM12878	blood:	n/a	n/a
11	BACH1	chr1:246537445-246537545	K562	blood:	n/a	n/a
12	BATF	chr1:246501825-246502142	GM12878	blood:	n/a	n/a
13	BATF	chr1:246493051-246493632	GM12878	blood:	n/a	chr1:246493346-246493357
14	BATF	chr1:246493105-246493597	GM12878	blood:	n/a	chr1:246493346-246493357
15	BCL11A	chr1:246493003-246493636	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
16	BCL11A	chr1:246493088-246493638	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
17	BCL3	chr1:246493055-246493585	GM12878	blood:	n/a	chr1:246493349-246493358
18	BCL3	chr1:246500317-246500521	GM12878	blood:	n/a	n/a
19	BCLAF1	chr1:246493000-246493668	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
20	BCLAF1	chr1:246493053-246493656	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
21	BHLHE40	chr1:246495569-246495766	K562	blood:	n/a	n/a
22	BHLHE40	chr1:246493081-246493626	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:246501485-246501808	K562	blood:	n/a	n/a
24	BHLHE40	chr1:246501857-246502115	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:246506768-246506903	GM12878	blood:	n/a	n/a
26	CCNT2	chr1:246495455-246495669	K562	blood:	n/a	n/a
27	CCNT2	chr1:246514072-246514334	K562	blood:	n/a	n/a
28	CEBPB	chr1:246530442-246530743	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:246501582-246501763	K562	blood:	n/a	n/a
30	CEBPB	chr1:246493011-246493799	GM12878	blood:	n/a	n/a
31	CEBPB	chr1:246495527-246495684	K562	blood:	n/a	n/a
32	CEBPD	chr1:246495352-246495831	K562	blood:	n/a	n/a
33	CHD2	chr1:246493191-246493493	GM12878	blood:	n/a	n/a
34	CREB1	chr1:246493043-246493660	GM12878	blood:	n/a	n/a
35	CREB1	chr1:246501712-246502306	GM12878	blood:	n/a	n/a
36	CREB1	chr1:246492960-246493710	GM12878	blood:	n/a	n/a
37	CREB1	chr1:246501915-246502173	GM12878	blood:	n/a	n/a
38	CTCF	chr1:246519100-246519250	A549	lung:	n/a	n/a
39	CTCF	chr1:246519040-246519190	GM12872	blood:	n/a	n/a
40	CTCF	chr1:246493460-246493610	GM12872	blood:	n/a	n/a
41	CTCF	chr1:246519020-246519170	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr1:246519020-246519170	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr1:246518891-246518922	Fibrobl	skin:	n/a	n/a
44	CTCF	chr1:246508820-246508970	GM12872	blood:	n/a	n/a
45	CTCF	chr1:246519128-246519179	ProgFib	skin:	n/a	n/a
46	CTCF	chr1:246519020-246519170	HAc	cerebellar:	n/a	n/a
47	CTCF	chr1:246518980-246519130	HCT-116	colon:	n/a	n/a
48	CTCF	chr1:246519080-246519230	HepG2	liver:	n/a	n/a
49	CTCF	chr1:246518961-246519268	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:246519100-246519250	GM12871	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246518671-246518721	BE2_C	brain:	n/a
2	chr1:246518671-246518721	HCPEpiC	choroid plexus:	n/a
3	chr1:246518620-246518670	T-47D	breast:	n/a
4	chr1:246518671-246518721	PrEC	prostate:	n/a
5	chr1:246518671-246518721	HAEpiC	amniotic membrane:	n/a
6	chr1:246518620-246518670	HIPEpiC	eye:	n/a
7	chr1:246518620-246518670	HUVEC	blood vessel:	n/a
8	chr1:246518671-246518721	T-47D	breast:	n/a
9	chr1:246518620-246518670	AG04449	skin:	fetal
10	chr1:246518620-246518670	NT2-D1	testis:	n/a
11	chr1:246518671-246518721	LNCaP	prostate:	n/a
12	chr1:246518671-246518721	HepG2	liver:	n/a
13	chr1:246518620-246518670	BE2_C	brain:	n/a
14	chr1:246518620-246518670	GM12878	blood:	n/a
15	chr1:246518620-246518670	AG10803	skin:	n/a
16	chr1:246518620-246518670	AoSMC	blood vessel:	n/a
17	chr1:246518671-246518721	NHDF-neo	bronchial:	n/a
18	chr1:246518671-246518721	HIPEpiC	eye:	n/a
19	chr1:246518620-246518670	Jurkat	blood:	n/a
20	chr1:246518620-246518670	AG09309	skin:	n/a
21	chr1:246518620-246518670	SK-N-SH	brain:	n/a
22	chr1:246518620-246518670	K562	blood:	n/a
23	chr1:246518620-246518670	U87	brain:	n/a
24	chr1:246518671-246518721	HCM	heart:	n/a
25	chr1:246518671-246518721	ProgFib	skin:	n/a
26	chr1:246518671-246518721	GM12878	blood:	n/a
27	chr1:246518620-246518670	GM19239	blood:	n/a
28	chr1:246518671-246518721	AG09309	skin:	n/a
29	chr1:246518671-246518721	HL-60	blood:	n/a
30	chr1:246518620-246518670	AG04450	lung:	fetal
31	chr1:246518671-246518721	NB4	blood:	n/a
32	chr1:246518620-246518670	HepG2	liver:	n/a
33	chr1:246518671-246518721	AG09319	gingival:	n/a
34	chr1:246518671-246518721	ECC-1	luminal epithelium:	n/a
35	chr1:246518620-246518670	CMK	blood:	n/a
36	chr1:246518620-246518670	HCM	heart:	n/a
37	chr1:246518620-246518670	NHBE	bronchial:	n/a
38	chr1:246518620-246518670	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:246518671-246518721	Jurkat	blood:	n/a
40	chr1:246518671-246518721	HEEpiC	esophagus:	n/a
41	chr1:246518671-246518721	IMR90	lung:	fetal
42	chr1:246518671-246518721	NHBE	bronchial:	n/a
43	chr1:246518671-246518721	ovcar-3	ovarian:	n/a
44	chr1:246518620-246518670	HL-60	blood:	n/a
45	chr1:246518671-246518721	HCF	heart:	n/a
46	chr1:246518620-246518670	RPTEC	kidney:	n/a
47	chr1:246518671-246518721	AG10803	skin:	n/a
48	chr1:246518671-246518721	PFSK-1	brain:	n/a
49	chr1:246518671-246518721	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:246518620-246518670	NB4	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246513035..246514840-chr1:246515014..246517355,2	K562	blood:
2	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:
3	chr1:246521302..246522820-chr1:246527857..246530408,2	K562	blood:
4	chr1:246513035..246514840-chr1:246515014..246517355,2	K562	blood:
5	chr1:246478448..246480701-chr1:246489976..246492079,2	MCF-7	breast:
6	chr1:246513912..246515911-chr1:246530351..246532425,2	K562	blood:
7	chr1:246513912..246515911-chr1:246530351..246532425,2	K562	blood:
8	chr1:246536157..246539066-chr1:246540727..246542818,2	K562	blood:
9	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:
10	chr1:246057307..246059352-chr1:246513090..246515764,2	K562	blood:
11	chr1:246521302..246522820-chr1:246527857..246530408,2	K562	blood:

No data

Variant related genes	Relation type
SMYD3	TF binding region
SMYD3	CpG island

Extended variants
information (count: 1685 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1685 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545272136	chr1:246491839-246491840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565602409	chr1:246491841-246491842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565952072	chr1:246491918-246491919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34546530	chr1:246491925-246491926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs201447584	chr1:246491947-246491948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544471312	chr1:246491956-246491957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560970079	chr1:246492090-246492091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529991564	chr1:246492143-246492144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546699000	chr1:246492164-246492165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566843440	chr1:246492173-246492174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532365245	chr1:246492175-246492176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs36057329	chr1:246492202-246492203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs568998821	chr1:246492206-246492207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538158301	chr1:246492213-246492214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201594933	chr1:246492218-246492219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568070366	chr1:246492224-246492225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6660473	chr1:246492262-246492263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533757991	chr1:246492313-246492314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553876373	chr1:246492338-246492339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201771624	chr1:246492369-246492370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539258182	chr1:246492384-246492385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558903167	chr1:246492393-246492394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10754509	chr1:246492432-246492433	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs201195447	chr1:246492472-246492473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561206767	chr1:246492497-246492498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574533665	chr1:246492640-246492641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186465358	chr1:246492698-246492699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560669770	chr1:246492737-246492738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532514372	chr1:246492750-246492751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10924693	chr1:246492769-246492770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375844389	chr1:246492785-246492786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368248974	chr1:246492800-246492801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562543671	chr1:246492819-246492820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531492445	chr1:246492836-246492837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548542464	chr1:246492842-246492843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560870176	chr1:246492857-246492858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371366639	chr1:246492876-246492877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547065695	chr1:246493011-246493012	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113196702	chr1:246493034-246493035	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7514346	chr1:246493061-246493062	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs190501531	chr1:246493073-246493074	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7518705	chr1:246493074-246493075	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs183105331	chr1:246493095-246493096	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117852309	chr1:246493096-246493097	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554891167	chr1:246493097-246493098	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187608385	chr1:246493128-246493129	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191364708	chr1:246493178-246493179	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560305529	chr1:246493236-246493237	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7518917	chr1:246493262-246493263	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs545988675	chr1:246493279-246493280	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	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
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246423400-246509000	Weak transcription	Aorta	Aorta
2	chr1:246441800-246506600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:246447600-246502800	Weak transcription	Left Ventricle	heart
4	chr1:246455000-246493000	Weak transcription	Primary B cells from cord blood	blood
5	chr1:246461800-246493000	Weak transcription	Primary T cells from cord blood	blood
6	chr1:246465600-246518800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:246470400-246493000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:246473400-246519200	Weak transcription	Pancreas	Pancrea
9	chr1:246474600-246504800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:246481000-246507400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:246481600-246493000	Weak transcription	Osteobl	bone
12	chr1:246482800-246494400	Weak transcription	Fetal Lung	lung
13	chr1:246483000-246493200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:246483400-246493200	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr1:246483600-246496200	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr1:246484400-246493000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr1:246484400-246498400	Weak transcription	Liver	Liver
18	chr1:246484600-246493000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:246484600-246501400	Weak transcription	HUVEC	blood vessel
20	chr1:246484800-246493200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr1:246486600-246497600	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr1:246488200-246492000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:246488200-246493000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:246488200-246493200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr1:246488200-246493200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr1:246488200-246493200	Weak transcription	Primary B cells from peripheral blood	blood
27	chr1:246488200-246493200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr1:246488400-246493200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr1:246488400-246497000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:246488400-246518600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:246488400-246518600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:246488600-246496600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr1:246488800-246493200	Weak transcription	Dnd41	blood
34	chr1:246489000-246493000	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr1:246490000-246499200	Weak transcription	Colonic Mucosa	Colon
36	chr1:246490200-246499600	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr1:246490400-246493000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr1:246490400-246500200	Weak transcription	Brain Substantia Nigra	brain
39	chr1:246491200-246509000	Weak transcription	A549	lung
40	chr1:246491600-246493200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr1:246492000-246503000	Weak transcription	Psoas Muscle	Psoas
42	chr1:246493000-246493600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:246493000-246493600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
44	chr1:246493000-246493600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:246493000-246493600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:246493000-246493600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:246493000-246493600	Strong transcription	Duodenum Smooth Muscle	Duodenum
48	chr1:246493000-246493800	Strong transcription	Osteobl	bone
49	chr1:246493000-246494000	Enhancers	GM12878-XiMat	blood
50	chr1:246493000-246495800	Strong transcription	Primary B cells from cord blood	blood

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