Variant report

Variant	esv3344128
Chromosome Location	chr4:737477-740825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:20)
CpG islands
(count:489)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:737593-737931	IMR90	lung:	n/a	chr4:737741-737754
2	CEBPB	chr4:737732-737835	HepG2	liver:	n/a	chr4:737741-737754
3	EGR1	chr4:738284-738523	K562	blood:	n/a	n/a
4	MYC	chr4:737773-738022	MCF10A-Er-Src	breast:	n/a	chr4:737866-737876
5	POLR2A	chr4:738004-738238	MCF-7	breast:	n/a	n/a
6	POLR2A	chr4:740585-740696	GM12878	blood:	n/a	n/a
7	POLR2A	chr4:738424-738652	GM12878	blood:	n/a	n/a
8	POLR2A	chr4:737880-737939	K562	blood:	n/a	n/a
9	POLR2A	chr4:738210-738220	K562	blood:	n/a	n/a
10	POLR2A	chr4:737553-737599	K562	blood:	n/a	n/a
11	POLR2A	chr4:738459-738507	A549	lung:	n/a	n/a
12	POLR2A	chr4:737826-738001	K562	blood:	n/a	n/a
13	POLR2A	chr4:738444-738660	GM12878	blood:	n/a	n/a
14	SP1	chr4:738405-738706	GM12878	blood:	n/a	n/a
15	TCF3	chr4:740546-740928	GM12878	blood:	n/a	n/a
16	TCF3	chr4:738368-738823	GM12878	blood:	n/a	n/a
17	TCF3	chr4:739494-739733	GM12878	blood:	n/a	n/a
18	TCF3	chr4:740034-740274	GM12878	blood:	n/a	n/a
19	TCF3	chr4:738970-739161	GM12878	blood:	n/a	n/a
20	TCF7L2	chr4:738047-738486	PANC-1	pancreas:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:738115-738165	IMR90	lung:	fetal
2	chr4:738115-738165	IMR90	lung:	fetal
3	chr4:739962-740012	HEK293	kidney:	embryo
4	chr4:738661-738711	HEK293	kidney:	embryo
5	chr4:738172-738222	ovcar-3	ovarian:	n/a
6	chr4:738172-738222	AG09319	gingival:	n/a
7	chr4:738115-738165	NHDF-neo	bronchial:	n/a
8	chr4:739607-739657	U87	brain:	n/a
9	chr4:738115-738165	HCF	heart:	n/a
10	chr4:737930-737980	AG04449	skin:	fetal
11	chr4:739962-740012	IMR90	lung:	fetal
12	chr4:738661-738711	H1-hESC	embryonic stem cell:	embryo
13	chr4:739962-740012	HRCEpiC	kidney:	n/a
14	chr4:738172-738222	HRE	kidney:	n/a
15	chr4:738661-738711	GM12892	blood:	n/a
16	chr4:739962-740012	HRPEpiC	eye:	n/a
17	chr4:738661-738711	HCT-116	colon:	n/a
18	chr4:738172-738222	HMEC	breast:	n/a
19	chr4:737453-737503	GM06990	blood:	n/a
20	chr4:737930-737980	GM06990	blood:	n/a
21	chr4:739962-740012	LNCaP	prostate:	n/a
22	chr4:738115-738165	Hepatocyte	liver:	n/a
23	chr4:739962-740012	PFSK-1	brain:	n/a
24	chr4:738115-738165	NHBE	bronchial:	n/a
25	chr4:739607-739657	HRPEpiC	eye:	n/a
26	chr4:738172-738222	SK-N-MC	brain:	n/a
27	chr4:738115-738165	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:737453-737503	HUVEC	blood vessel:	n/a
29	chr4:739962-740012	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:737930-737980	HAEpiC	amniotic membrane:	n/a
31	chr4:737453-737503	ProgFib	skin:	n/a
32	chr4:737930-737980	HIPEpiC	eye:	n/a
33	chr4:738199-738249	BJ	skin:	n/a
34	chr4:738199-738249	NHDF-neo	bronchial:	n/a
35	chr4:738115-738165	HIPEpiC	eye:	n/a
36	chr4:737930-737980	Hela-S3	cervix:	n/a
37	chr4:739962-740012	GM12891	blood:	n/a
38	chr4:738115-738165	BJ	skin:	n/a
39	chr4:737453-737503	Caco-2	colon:	n/a
40	chr4:738172-738222	BJ	skin:	n/a
41	chr4:738115-738165	GM06990	blood:	n/a
42	chr4:739607-739657	HCF	heart:	n/a
43	chr4:739607-739657	GM06990	blood:	n/a
44	chr4:738172-738222	GM12891	blood:	n/a
45	chr4:737930-737980	LNCaP	prostate:	n/a
46	chr4:738661-738711	AG09309	skin:	n/a
47	chr4:738661-738711	HRPEpiC	eye:	n/a
48	chr4:738172-738222	AG09309	skin:	n/a
49	chr4:737930-737980	Caco-2	colon:	n/a
50	chr4:739607-739657	SK-N-SH_RA	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:678244..681266-chr4:735203..738855,3	MCF-7	breast:
2	chr4:732543..739360-chr4:740100..745945,6	K562	blood:
3	chr4:735917..738355-chr4:773628..776647,3	MCF-7	breast:
4	chr4:735427..738255-chr4:740119..742339,2	MCF-7	breast:
5	chr4:735724..738302-chr4:774438..777111,2	MCF-7	breast:

No data

Variant related genes	Relation type
PCGF3	TF binding region
PCGF3	CpG island
ENSG00000169026	chromatin interactions
ENSG00000185619	chromatin interactions
ENSG00000249592	chromatin interactions

Extended variants
information (count: 140 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:140 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201133887	chr4:737486-737487	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs370487830	chr4:737493-737494	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs145849636	chr4:737532-737533	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs191936133	chr4:737542-737543	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs2279174	chr4:737596-737597	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs563576024	chr4:737599-737600	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs527251941	chr4:737601-737602	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs531033778	chr4:737602-737603	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs4690298	chr4:737643-737644	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs116513518	chr4:737651-737652	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs371890789	chr4:737654-737655	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs138688025	chr4:737661-737662	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546415005	chr4:737662-737663	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141133179	chr4:737735-737736	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs560152859	chr4:737736-737737	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs376575125	chr4:737738-737739	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs538595117	chr4:737800-737801	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs550546363	chr4:737848-737849	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs568713119	chr4:737883-737884	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs536253259	chr4:737901-737902	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs150483411	chr4:737903-737904	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs572996656	chr4:737904-737905	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs201258971	chr4:737931-737932	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs553639641	chr4:737934-737935	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs578190745	chr4:737965-737966	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545426590	chr4:737990-737991	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs557640013	chr4:738032-738033	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs575513563	chr4:738083-738084	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542631380	chr4:738086-738087	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs561023541	chr4:738130-738131	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs528596062	chr4:738132-738133	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs540027465	chr4:738133-738134	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184186569	chr4:738142-738143	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564784123	chr4:738181-738182	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs560941166	chr4:738195-738196	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532337411	chr4:738220-738221	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs6835343	chr4:738226-738227	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs569148386	chr4:738236-738237	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs115663287	chr4:738243-738244	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs548236256	chr4:738251-738252	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543528200	chr4:738255-738256	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs566558873	chr4:738257-738258	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs188293738	chr4:738269-738270	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553603919	chr4:738273-738274	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs56187241	chr4:738275-738276	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs539210745	chr4:738320-738321	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs191725816	chr4:738337-738338	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs375495419	chr4:738345-738346	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532750373	chr4:738381-738382	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs183503213	chr4:738398-738399	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:702200-754800	Weak transcription	Hela-S3	cervix
2	chr4:715600-750200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:720000-738400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:720800-738400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:721000-738600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:721000-743600	Weak transcription	Right Atrium	heart
7	chr4:723600-738600	Strong transcription	Brain Germinal Matrix	brain
8	chr4:723800-737600	Strong transcription	Dnd41	blood
9	chr4:723800-738400	Strong transcription	Cortex derived primary cultured neurospheres	brain
10	chr4:724200-738600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:724200-738600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr4:725200-738400	Strong transcription	Thymus	Thymus
13	chr4:725200-738600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:725200-738600	Strong transcription	Fetal Stomach	stomach
15	chr4:725800-738400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr4:725800-738600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:726200-738400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:726200-738400	Strong transcription	Placenta Amnion	Placenta Amnion
19	chr4:726200-738600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr4:727000-767600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr4:727200-738200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:728000-741800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr4:728600-755800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr4:728600-763400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr4:729000-742400	Weak transcription	Small Intestine	intestine
26	chr4:729000-754600	Weak transcription	Fetal Kidney	kidney
27	chr4:729000-762600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr4:729600-753800	Weak transcription	Psoas Muscle	Psoas
29	chr4:729600-760800	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr4:729800-738400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr4:729800-741600	Weak transcription	Rectal Smooth Muscle	rectum
32	chr4:732000-742400	Weak transcription	NHDF-Ad	bronchial
33	chr4:732000-745200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr4:732200-741800	Weak transcription	K562	blood
35	chr4:732200-743600	Weak transcription	HMEC	breast
36	chr4:733400-738400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr4:733600-738400	Strong transcription	Fetal Intestine Small	intestine
38	chr4:733600-741600	Weak transcription	Brain Angular Gyrus	brain
39	chr4:733600-741600	Weak transcription	GM12878-XiMat	blood
40	chr4:733600-742600	Weak transcription	Stomach Mucosa	stomach
41	chr4:733600-753800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr4:733800-747400	Weak transcription	Primary B cells from cord blood	blood
43	chr4:734000-741600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr4:734000-744000	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr4:734000-745400	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr4:734200-741800	Weak transcription	Colon Smooth Muscle	Colon
47	chr4:734200-744800	Weak transcription	Brain Cingulate Gyrus	brain
48	chr4:734400-741400	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr4:734400-741800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr4:734400-745400	Weak transcription	Brain Hippocampus Middle	brain

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