Variant report

Variant	nsv967784
Chromosome Location	chr4:110594675-110601981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:94)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:94 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr4:110599998-110600212	K562	blood:	n/a	n/a
2	CTCF	chr4:110598200-110598350	HRPEpiC	eye:	n/a	n/a
3	CTCF	chr4:110598169-110598269	MCF-7	breast:	n/a	n/a
4	CTCF	chr4:110598180-110598330	AG09309	skin:	n/a	n/a
5	CTCF	chr4:110598214-110598276	Spleen_OC	spleen:	n/a	n/a
6	CTCF	chr4:110598140-110598290	HMF	breast:	n/a	n/a
7	CTCF	chr4:110598100-110598250	GM12872	blood:	n/a	n/a
8	CTCF	chr4:110598180-110598330	GM06990	blood:	n/a	n/a
9	CTCF	chr4:110598200-110598350	GM12872	blood:	n/a	n/a
10	CTCF	chr4:110598160-110598310	AG10803	skin:	n/a	n/a
11	CTCF	chr4:110598143-110598303	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:110598181-110598272	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr4:110598152-110598317	MCF-7	breast:	n/a	n/a
14	CTCF	chr4:110598200-110598350	K562	blood:	n/a	n/a
15	CTCF	chr4:110598200-110598350	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr4:110598180-110598330	BJ	skin:	n/a	n/a
17	CTCF	chr4:110598100-110598250	SAEC	small airway:	n/a	n/a
18	CTCF	chr4:110598220-110598370	AG09309	skin:	n/a	n/a
19	CTCF	chr4:110598140-110598290	GM12874	blood:	n/a	n/a
20	CTCF	chr4:110598120-110598270	HMEC	breast:	n/a	n/a
21	CTCF	chr4:110598200-110598350	HVMF	connective:	n/a	n/a
22	CTCF	chr4:110598100-110598250	HAc	cerebellar:	n/a	n/a
23	CTCF	chr4:110598160-110598310	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr4:110598120-110598270	GM12871	blood:	n/a	n/a
25	CTCF	chr4:110598115-110598402	K562	blood:	n/a	n/a
26	CTCF	chr4:110598180-110598330	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr4:110598420-110598570	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr4:110598060-110598210	GM12871	blood:	n/a	n/a
29	CTCF	chr4:110598100-110598250	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr4:110598160-110598310	GM12878	blood:	n/a	n/a
31	CTCF	chr4:110598188-110598265	A549	lung:	n/a	n/a
32	CTCF	chr4:110598200-110598350	AG09319	gingival:	n/a	n/a
33	CTCF	chr4:110598287-110598290	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr4:110598150-110598488	HCT-116	colon:	n/a	n/a
35	CTCF	chr4:110598177-110598273	GM12892	blood:	n/a	n/a
36	CTCF	chr4:110598200-110598350	HCT-116	colon:	n/a	n/a
37	CTCF	chr4:110598213-110598217	GM10266	blood:	n/a	n/a
38	CTCF	chr4:110598168-110598310	GM12878	blood:	n/a	n/a
39	CTCF	chr4:110598200-110598350	HCFaa	heart:	n/a	n/a
40	CTCF	chr4:110598179-110598249	ProgFib	skin:	n/a	n/a
41	CTCF	chr4:110598160-110598310	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr4:110598158-110598284	GM19240	blood:	n/a	n/a
43	CTCF	chr4:110598234-110598244	GM10266	blood:	n/a	n/a
44	CTCF	chr4:110598197-110598230	Fibrobl	skin:	n/a	n/a
45	CTCF	chr4:110598120-110598270	GM12875	blood:	n/a	n/a
46	CTCF	chr4:110598170-110598270	GM19238	blood:	n/a	n/a
47	CTCF	chr4:110598124-110598359	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:110598180-110598330	SAEC	small airway:	n/a	n/a
49	CTCF	chr4:110598140-110598290	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:110598200-110598350	HCPEpiC	choroid plexus:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110599688-110599738	PANC-1	pancreas:	n/a
2	chr4:110600020-110600070	NH-A	brain:	n/a
3	chr4:110600020-110600070	HUVEC	blood vessel:	n/a
4	chr4:110599688-110599738	GM12878	blood:	n/a
5	chr4:110600020-110600070	SK-N-MC	brain:	n/a
6	chr4:110600020-110600070	GM12878	blood:	n/a
7	chr4:110599688-110599738	HepG2	liver:	n/a
8	chr4:110600020-110600070	SK-N-SH	brain:	n/a
9	chr4:110599688-110599738	GM12892	blood:	n/a
10	chr4:110600020-110600070	T-47D	breast:	n/a
11	chr4:110600020-110600070	PANC-1	pancreas:	n/a
12	chr4:110600020-110600070	HIPEpiC	eye:	n/a
13	chr4:110599688-110599738	HEEpiC	esophagus:	n/a
14	chr4:110600020-110600070	NB4	blood:	n/a
15	chr4:110600020-110600070	HCM	heart:	n/a
16	chr4:110599688-110599738	SAEC	small airway:	n/a
17	chr4:110599688-110599738	SK-N-MC	brain:	n/a
18	chr4:110599688-110599738	GM19239	blood:	n/a
19	chr4:110600020-110600070	HEEpiC	esophagus:	n/a
20	chr4:110599688-110599738	SKMC	muscle:	n/a
21	chr4:110599688-110599738	Hepatocyte	liver:	n/a
22	chr4:110600020-110600070	CMK	blood:	n/a
23	chr4:110599688-110599738	RPTEC	kidney:	n/a
24	chr4:110599688-110599738	HUVEC	blood vessel:	n/a
25	chr4:110600020-110600070	RPTEC	kidney:	n/a
26	chr4:110600020-110600070	AG04449	skin:	fetal
27	chr4:110599688-110599738	HNPCEpiC	eye:	n/a
28	chr4:110599688-110599738	SK-N-SH	brain:	n/a
29	chr4:110599688-110599738	HCM	heart:	n/a
30	chr4:110600020-110600070	BE2_C	brain:	n/a
31	chr4:110599688-110599738	NH-A	brain:	n/a
32	chr4:110599688-110599738	AoSMC	blood vessel:	n/a
33	chr4:110600020-110600070	Caco-2	colon:	n/a
34	chr4:110600020-110600070	HNPCEpiC	eye:	n/a
35	chr4:110599688-110599738	NHDF-neo	bronchial:	n/a
36	chr4:110599688-110599738	CMK	blood:	n/a
37	chr4:110599688-110599738	HAEpiC	amniotic membrane:	n/a
38	chr4:110599688-110599738	U87	brain:	n/a
39	chr4:110599688-110599738	BJ	skin:	n/a
40	chr4:110600020-110600070	SAEC	small airway:	n/a
41	chr4:110600020-110600070	AG04450	lung:	fetal
42	chr4:110599688-110599738	HIPEpiC	eye:	n/a
43	chr4:110600020-110600070	Hela-S3	cervix:	n/a
44	chr4:110599688-110599738	NB4	blood:	n/a
45	chr4:110599688-110599738	AG04449	skin:	fetal
46	chr4:110599688-110599738	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:110599688-110599738	Jurkat	blood:	n/a
48	chr4:110600020-110600070	AoSMC	blood vessel:	n/a
49	chr4:110599688-110599738	HMEC	breast:	n/a
50	chr4:110600020-110600070	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:110596739..110598343-chr4:110599981..110601558,2	MCF-7	breast:
2	chr4:110596739..110598343-chr4:110599981..110601558,2	MCF-7	breast:
3	chr4:110353199..110355623-chr4:110596847..110599552,2	MCF-7	breast:
4	chr4:110597890..110598667-chr4:110725301..110725981,3	MCF-7	breast:
5	chr4:110592093..110594740-chr4:110602207..110604026,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEC24B-2	chr4:110594999-110595280	NONHSAT097790

No data

Variant related genes	Relation type
CCDC109B	TF binding region
HIGD1AP14	TF binding region
CCDC109B	CpG island
HIGD1AP14	CpG island
ENSG00000138802	chromatin interactions
ENSG00000247950	chromatin interactions

Extended variants
information (count: 272 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377369503	chr4:110594732-110594733	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs564191638	chr4:110594750-110594751	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs570753835	chr4:110594798-110594799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374130147	chr4:110594945-110594946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530748911	chr4:110594950-110594951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539247184	chr4:110594953-110594954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs61735996	chr4:110595005-110595006	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs182835969	chr4:110595026-110595027	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs59905504	chr4:110595062-110595063	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs188135264	chr4:110595085-110595086	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs10488887	chr4:110595086-110595087	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs374872594	chr4:110595100-110595101	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs56107497	chr4:110595143-110595144	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs528113163	chr4:110595173-110595174	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs149936581	chr4:110595177-110595178	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs560600957	chr4:110595186-110595187	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs374707910	chr4:110595189-110595190	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs191244186	chr4:110595197-110595198	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs546409268	chr4:110595221-110595222	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs183530521	chr4:110595264-110595265	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs115440293	chr4:110595286-110595287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548410660	chr4:110595299-110595300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144982031	chr4:110595306-110595307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567850181	chr4:110595392-110595393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527665356	chr4:110595403-110595404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187403570	chr4:110595407-110595408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112424612	chr4:110595490-110595491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111761723	chr4:110595527-110595528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539360438	chr4:110595581-110595582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192095385	chr4:110595658-110595659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185035699	chr4:110595689-110595690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114133436	chr4:110595698-110595699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555151971	chr4:110595699-110595700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572133354	chr4:110595768-110595769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540665219	chr4:110595785-110595786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60211464	chr4:110595830-110595831	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs114612812	chr4:110595833-110595834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546542073	chr4:110595836-110595837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35727499	chr4:110595866-110595867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs57136696	chr4:110595872-110595873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576696524	chr4:110595884-110595885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367596125	chr4:110595980-110595981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542439092	chr4:110595998-110595999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562040829	chr4:110596029-110596030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12503489	chr4:110596074-110596075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527828989	chr4:110596124-110596125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547437597	chr4:110596128-110596129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140500765	chr4:110596133-110596134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533026650	chr4:110596160-110596161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143635979	chr4:110596180-110596181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Esophageal cancer	21851588	CNVD
Melanoma	20688739	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110571000-110605400	Weak transcription	Left Ventricle	heart
2	chr4:110572600-110623200	Weak transcription	Esophagus	oesophagus
3	chr4:110574200-110598400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr4:110579200-110608400	Weak transcription	Ovary	ovary
5	chr4:110581600-110596800	Weak transcription	Lung	lung
6	chr4:110583000-110596600	Weak transcription	HepG2	liver
7	chr4:110583600-110605600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr4:110584200-110606000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:110584400-110608800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:110585200-110596800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:110585200-110599600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:110585800-110608800	Weak transcription	Adipose Nuclei	Adipose
13	chr4:110586000-110599800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr4:110586000-110605200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr4:110589600-110623200	Weak transcription	Brain Substantia Nigra	brain
16	chr4:110590200-110602600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:110590600-110606000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr4:110591200-110602600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr4:110591200-110608600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr4:110591600-110605000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr4:110592000-110611600	Weak transcription	Rectal Smooth Muscle	rectum
22	chr4:110592200-110599600	Weak transcription	Thymus	Thymus
23	chr4:110592600-110596400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr4:110592800-110603800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr4:110593000-110594800	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr4:110593000-110596200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr4:110593000-110596800	Strong transcription	Dnd41	blood
28	chr4:110593000-110598400	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr4:110593000-110600000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:110593000-110601400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr4:110593000-110608200	Weak transcription	Fetal Lung	lung
32	chr4:110593200-110596200	Weak transcription	GM12878-XiMat	blood
33	chr4:110593200-110596600	Weak transcription	Primary hematopoietic stem cells	blood
34	chr4:110593200-110597000	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr4:110593200-110600200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:110593800-110594800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:110593800-110611600	Weak transcription	K562	blood
38	chr4:110594200-110594800	Strong transcription	Primary B cells from cord blood	blood
39	chr4:110594200-110597000	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr4:110594200-110601800	Weak transcription	Primary B cells from peripheral blood	blood
41	chr4:110594400-110595200	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr4:110594400-110595200	Strong transcription	Fetal Thymus	thymus
43	chr4:110594400-110599000	Strong transcription	Primary T cells from cord blood	blood
44	chr4:110594600-110595200	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr4:110594800-110597600	Weak transcription	Primary B cells from cord blood	blood
46	chr4:110594800-110598600	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr4:110595200-110596600	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr4:110595200-110599600	Weak transcription	Fetal Thymus	thymus
49	chr4:110595200-110601400	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr4:110596200-110596600	Enhancers	GM12878-XiMat	blood

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