Variant report

Variant	nsv1011282
Chromosome Location	chr2:97731121-97854147
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1489)
CpG islands
(count:1771)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:97778812-97778979	K562	blood:	n/a	n/a
2	ARID3A	chr2:97778081-97778339	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:97778120-97778444	K562	blood:	n/a	n/a
4	ARID3A	chr2:97778807-97778948	HepG2	liver:	n/a	n/a
5	ATF1	chr2:97807805-97807929	K562	blood:	n/a	n/a
6	ATF1	chr2:97778135-97778323	K562	blood:	n/a	n/a
7	ATF1	chr2:97760434-97760794	K562	blood:	n/a	n/a
8	ATF3	chr2:97778056-97778311	GM12878	blood:	n/a	n/a
9	ATF3	chr2:97778756-97778914	K562	blood:	n/a	n/a
10	BACH1	chr2:97778797-97778986	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:97831358-97831389	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr2:97777979-97778283	GM12878	blood:	n/a	n/a
13	BATF	chr2:97760489-97760619	GM12878	blood:	n/a	n/a
14	BATF	chr2:97779034-97779410	GM12878	blood:	n/a	n/a
15	BATF	chr2:97759887-97760164	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:97780056-97780285	GM12878	blood:	n/a	n/a
17	BCL11A	chr2:97778042-97778304	GM12878	blood:	n/a	chr2:97778076-97778083
18	BCL11A	chr2:97778616-97779385	GM12878	blood:	n/a	chr2:97778799-97778812 chr2:97778886-97778899
19	BCL11A	chr2:97759908-97760372	GM12878	blood:	n/a	n/a
20	BCLAF1	chr2:97778704-97779122	GM12878	blood:	n/a	chr2:97778799-97778812 chr2:97778886-97778899
21	BHLHE40	chr2:97778115-97778317	GM12878	blood:	n/a	n/a
22	BHLHE40	chr2:97778670-97778987	GM12878	blood:	n/a	chr2:97778882-97778898
23	BHLHE40	chr2:97778996-97779445	HepG2	liver:	n/a	n/a
24	BHLHE40	chr2:97778783-97778959	K562	blood:	n/a	chr2:97778882-97778898
25	BRCA1	chr2:97779217-97779560	Hela-S3	cervix:	n/a	chr2:97779322-97779329
26	BRCA1	chr2:97778112-97778312	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr2:97760435-97760807	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr2:97779000-97779465	K562	blood:	n/a	n/a
29	CBX3	chr2:97778594-97779624	K562	blood:	n/a	n/a
30	CBX3	chr2:97760424-97760767	K562	blood:	n/a	n/a
31	CBX3	chr2:97764654-97764925	K562	blood:	n/a	n/a
32	CBX3	chr2:97778007-97778486	K562	blood:	n/a	n/a
33	CEBPB	chr2:97773450-97773635	HepG2	liver:	n/a	chr2:97773565-97773576
34	CEBPB	chr2:97773446-97773645	IMR90	lung:	n/a	chr2:97773565-97773576
35	CEBPB	chr2:97779104-97779603	K562	blood:	n/a	n/a
36	CEBPB	chr2:97778777-97779401	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:97773440-97773636	K562	blood:	n/a	chr2:97773565-97773576
38	CEBPB	chr2:97773431-97773709	K562	blood:	n/a	chr2:97773565-97773576
39	CEBPB	chr2:97799578-97799766	HepG2	liver:	n/a	chr2:97799651-97799662
40	CEBPD	chr2:97778691-97779170	HepG2	liver:	n/a	n/a
41	CEBPD	chr2:97778701-97779156	K562	blood:	n/a	n/a
42	CHD2	chr2:97760599-97760634	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr2:97778828-97779405	HepG2	liver:	n/a	chr2:97779346-97779356
44	CHD2	chr2:97778790-97779380	GM12878	blood:	n/a	chr2:97779346-97779356
45	CHD2	chr2:97778673-97779488	Hela-S3	cervix:	n/a	chr2:97779346-97779356
46	CREB1	chr2:97760524-97760708	A549	lung:	n/a	n/a
47	CREB1	chr2:97760499-97760714	A549	lung:	n/a	n/a
48	CREB1	chr2:97778691-97779100	A549	lung:	n/a	n/a
49	CREB1	chr2:97760530-97760694	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr2:97778000-97778150	HCT-116	colon:	n/a	n/a

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:97778817-97778867	HCT-116	colon:	n/a
2	chr2:97779411-97779461	NT2-D1	testis:	n/a
3	chr2:97778817-97778867	HCT-116	colon:	n/a
4	chr2:97779411-97779461	NT2-D1	testis:	n/a
5	chr2:97778608-97778658	GM12878	blood:	n/a
6	chr2:97763993-97764043	GM12891	blood:	n/a
7	chr2:97778817-97778867	HRCEpiC	kidney:	n/a
8	chr2:97759501-97759551	HCT-116	colon:	n/a
9	chr2:97760622-97760672	HRE	kidney:	n/a
10	chr2:97760749-97760799	HMEC	breast:	n/a
11	chr2:97779044-97779094	HL-60	blood:	n/a
12	chr2:97779784-97779834	HEK293	kidney:	embryo
13	chr2:97760610-97760660	HNPCEpiC	eye:	n/a
14	chr2:97760749-97760799	HRE	kidney:	n/a
15	chr2:97759501-97759551	IMR90	lung:	fetal
16	chr2:97779784-97779834	HCPEpiC	choroid plexus:	n/a
17	chr2:97775474-97775524	U87	brain:	n/a
18	chr2:97783139-97783189	Hela-S3	cervix:	n/a
19	chr2:97776919-97776969	GM19239	blood:	n/a
20	chr2:97760622-97760672	HepG2	liver:	n/a
21	chr2:97760726-97760776	SKMC	muscle:	n/a
22	chr2:97778470-97778520	HRCEpiC	kidney:	n/a
23	chr2:97776919-97776969	GM12891	blood:	n/a
24	chr2:97760745-97760795	NHBE	bronchial:	n/a
25	chr2:97760749-97760799	NB4	blood:	n/a
26	chr2:97778927-97778977	HAEpiC	amniotic membrane:	n/a
27	chr2:97778912-97778962	GM12891	blood:	n/a
28	chr2:97760612-97760662	HIPEpiC	eye:	n/a
29	chr2:97761843-97761893	LNCaP	prostate:	n/a
30	chr2:97760612-97760662	AG04449	skin:	fetal
31	chr2:97761334-97761384	HEK293	kidney:	embryo
32	chr2:97778608-97778658	AG10803	skin:	n/a
33	chr2:97779433-97779483	GM19239	blood:	n/a
34	chr2:97759501-97759551	NHBE	bronchial:	n/a
35	chr2:97763993-97764043	Hela-S3	cervix:	n/a
36	chr2:97775474-97775524	GM12891	blood:	n/a
37	chr2:97779565-97779615	MCF-7	breast:	n/a
38	chr2:97760612-97760662	GM12892	blood:	n/a
39	chr2:97760612-97760662	NHBE	bronchial:	n/a
40	chr2:97760610-97760660	HEK293	kidney:	embryo
41	chr2:97778817-97778867	SK-N-MC	brain:	n/a
42	chr2:97760610-97760660	ProgFib	skin:	n/a
43	chr2:97761334-97761384	HNPCEpiC	eye:	n/a
44	chr2:97760610-97760660	HCPEpiC	choroid plexus:	n/a
45	chr2:97778817-97778867	Caco-2	colon:	n/a
46	chr2:97760622-97760672	CMK	blood:	n/a
47	chr2:97746622-97746672	ECC-1	luminal epithelium:	n/a
48	chr2:97761354-97761404	AoSMC	blood vessel:	n/a
49	chr2:97779433-97779483	PFSK-1	brain:	n/a
50	chr2:97761843-97761893	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:97523665..97525724-chr2:97777402..97779360,2	MCF-7	breast:
2	chr2:97677657..97678211-chr2:97777841..97778623,2	K562	blood:
3	chr2:97405027..97406967-chr2:97777321..97779642,2	K562	blood:
4	chr2:97778136..97778658-chr2:114147633..114148424,9	MCF-7	breast:
5	chr2:97778139..97778659-chr2:114147598..114148210,2	K562	blood:
6	chr2:97522364..97524649-chr2:97747761..97749583,2	MCF-7	breast:
7	chr2:97522570..97524502-chr2:97776940..97779479,2	MCF-7	breast:
8	chr2:97625836..97626837-chr2:97777734..97778610,3	MCF-7	breast:
9	chr2:97753095..97754963-chr2:97759459..97762136,2	K562	blood:
10	chr2:97480158..97482561-chr2:97778545..97780856,2	MCF-7	breast:
11	chr2:97777932..97778642-chr2:114147602..114148330,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD36-5	chr2:97747330-97748385	NONHSAT072606
2	lnc-ANKRD36-3	chr2:97766321-97766609	NONHSAT072609

No data

Variant related genes	Relation type
FAHD2B	TF binding region
RN7SL313P	TF binding region
ANKRD36	TF binding region
ENSG00000188383	TF binding region
FAHD2B	CpG island
RN7SL313P	CpG island
ANKRD36	CpG island
ENSG00000188383	CpG island
ENSG00000213337	chromatin interactions
ENSG00000144199	chromatin interactions
ENSG00000163126	chromatin interactions
ENSG00000114988	chromatin interactions
ENSG00000168763	chromatin interactions

Extended variants
information (count: 4729 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4729 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139360400	chr2:97731843-97731844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs201118899	chr2:97731852-97731853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560352184	chr2:97731854-97731855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs199647438	chr2:97731863-97731864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574324516	chr2:97731876-97731877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182621125	chr2:97731885-97731886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114011318	chr2:97731887-97731888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532239726	chr2:97731915-97731916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150025205	chr2:97731918-97731919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562735526	chr2:97731957-97731958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531814027	chr2:97731968-97731969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187046507	chr2:97731997-97731998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs56678113	chr2:97732030-97732031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182107676	chr2:97732059-97732060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527643659	chr2:97732067-97732068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187632803	chr2:97732072-97732073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527711083	chr2:97732123-97732124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570803008	chr2:97732129-97732130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546176339	chr2:97732139-97732140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372444581	chr2:97732140-97732141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1148581	chr2:97732152-97732153	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
22	rs372955824	chr2:97732194-97732195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550331919	chr2:97732198-97732199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376973166	chr2:97732200-97732201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569053008	chr2:97732219-97732220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538061546	chr2:97732226-97732227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141396223	chr2:97732227-97732228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574686312	chr2:97732233-97732234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115059376	chr2:97732343-97732344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533510827	chr2:97732441-97732442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115955021	chr2:97732489-97732490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576806857	chr2:97732498-97732499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373404208	chr2:97732624-97732625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562263290	chr2:97732639-97732640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113274049	chr2:97732717-97732718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs193246541	chr2:97732726-97732727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2443829	chr2:97732729-97732730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542025049	chr2:97732732-97732733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78459140	chr2:97732751-97732752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113197708	chr2:97732752-97732753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2443828	chr2:97732762-97732763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2443827	chr2:97732770-97732771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79843497	chr2:97732785-97732786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562196277	chr2:97732786-97732787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75165896	chr2:97732788-97732789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78676202	chr2:97732812-97732813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112928392	chr2:97732821-97732822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs3028097	chr2:97732822-97732823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs35326451	chr2:97732823-97732824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs58986769	chr2:97732825-97732826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:97731800-97732200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:97732000-97732200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:97732200-97733200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:97732200-97733400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:97732600-97734800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr2:97733200-97733800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr2:97733200-97734000	ZNF genes & repeats	Gastric	stomach
8	chr2:97733200-97734200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:97733400-97733800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
10	chr2:97733400-97734000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:97733400-97734000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr2:97733600-97733800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
13	chr2:97733600-97734000	Enhancers	Brain Germinal Matrix	brain
14	chr2:97733800-97734000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:97733800-97734200	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr2:97734200-97738600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:97738600-97738800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:97744800-97745000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:97745000-97760600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:97746600-97759800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr2:97747000-97760600	Weak transcription	Fetal Muscle Leg	muscle
22	chr2:97747200-97760800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr2:97747400-97749200	Weak transcription	Fetal Stomach	stomach
24	chr2:97747600-97748600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr2:97747600-97749600	Enhancers	Esophagus	oesophagus
26	chr2:97747600-97759800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr2:97747800-97748000	Enhancers	Brain Hippocampus Middle	brain
28	chr2:97748000-97749400	Weak transcription	Brain Hippocampus Middle	brain
29	chr2:97748000-97759800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr2:97748000-97760400	Weak transcription	Ovary	ovary
31	chr2:97748000-97760400	Weak transcription	Right Ventricle	heart
32	chr2:97748000-97760600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr2:97748000-97760800	Weak transcription	Brain Substantia Nigra	brain
34	chr2:97748600-97756200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr2:97748600-97760800	Weak transcription	Brain Cingulate Gyrus	brain
36	chr2:97748600-97761000	Weak transcription	Primary T cells from cord blood	blood
37	chr2:97748800-97760600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr2:97749200-97750800	Strong transcription	Fetal Stomach	stomach
39	chr2:97749400-97750200	Strong transcription	Brain Hippocampus Middle	brain
40	chr2:97749800-97759600	Weak transcription	Fetal Brain Female	brain
41	chr2:97750200-97758800	Weak transcription	Brain Hippocampus Middle	brain
42	chr2:97750200-97760800	Weak transcription	Brain Anterior Caudate	brain
43	chr2:97750400-97759600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr2:97750400-97759800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr2:97750400-97760000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:97750400-97760400	Weak transcription	Left Ventricle	heart
47	chr2:97750600-97759800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:97750600-97760400	Weak transcription	Fetal Muscle Trunk	muscle
49	chr2:97750600-97761400	Weak transcription	Lung	lung
50	chr2:97750800-97757000	Weak transcription	Fetal Stomach	stomach

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