Variant report

Variant	nsv3031
Chromosome Location	chr2:172867462-172884232
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:171)
CpG islands
(count:61)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:171 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:172873713-172873935	K562	blood:	n/a	n/a
2	ATF2	chr2:172876754-172877091	GM12878	blood:	n/a	n/a
3	ATF2	chr2:172876621-172877079	GM12878	blood:	n/a	n/a
4	ATF3	chr2:172873499-172873996	HCT-116	colon:	n/a	n/a
5	ATF3	chr2:172873552-172873961	K562	blood:	n/a	n/a
6	ATF3	chr2:172873487-172873987	HCT-116	colon:	n/a	n/a
7	BACH1	chr2:172878446-172878732	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr2:172876834-172877071	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:172878376-172878694	GM12878	blood:	n/a	chr2:172878378-172878387
10	BHLHE40	chr2:172873771-172873832	K562	blood:	n/a	n/a
11	BHLHE40	chr2:172878397-172878805	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:172876767-172877034	GM12878	blood:	n/a	n/a
13	CBX3	chr2:172873529-172874075	HCT-116	colon:	n/a	n/a
14	CEBPB	chr2:172873640-172874065	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:172872399-172872593	HepG2	liver:	n/a	chr2:172872488-172872499
16	CEBPB	chr2:172872360-172872590	HepG2	liver:	n/a	chr2:172872488-172872499
17	CEBPB	chr2:172867330-172867617	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:172872323-172872638	HepG2	liver:	n/a	chr2:172872488-172872499
19	CEBPB	chr2:172873731-172873928	K562	blood:	n/a	n/a
20	CEBPB	chr2:172872313-172872676	HepG2	liver:	n/a	chr2:172872488-172872499
21	CHD2	chr2:172877277-172877371	K562	blood:	n/a	n/a
22	CHD2	chr2:172878158-172878195	HepG2	liver:	n/a	n/a
23	CHD2	chr2:172878592-172878639	GM12878	blood:	n/a	n/a
24	CTCF	chr2:172878194-172878249	GM12891	blood:	n/a	chr2:172878208-172878218
25	CTCF	chr2:172878120-172878270	HepG2	liver:	n/a	chr2:172878208-172878218
26	CTCF	chr2:172878117-172878274	MCF-7	breast:	n/a	chr2:172878208-172878218
27	CTCF	chr2:172878140-172878290	GM12875	blood:	n/a	chr2:172878208-172878218
28	CTCF	chr2:172878181-172878267	H1-hESC	embryonic stem cell:	n/a	chr2:172878208-172878218
29	CTCF	chr2:172878160-172878264	HepG2	liver:	n/a	chr2:172878208-172878218
30	CTCF	chr2:172878120-172878270	AG09319	gingival:	n/a	chr2:172878208-172878218
31	CTCF	chr2:172878157-172878261	MCF-7	breast:	n/a	chr2:172878208-172878218
32	CTCF	chr2:172878160-172878310	HFF-Myc	foreskin:	n/a	chr2:172878208-172878218
33	CTCF	chr2:172876238-172876288	LNCaP	prostate:	n/a	n/a
34	CTCF	chr2:172878208-172878233	MCF-7	breast:	n/a	chr2:172878208-172878218
35	EBF1	chr2:172878383-172878656	GM12878	blood:	n/a	n/a
36	EBF1	chr2:172878414-172878620	GM12878	blood:	n/a	n/a
37	EBF1	chr2:172878344-172878690	GM12878	blood:	n/a	n/a
38	ELF1	chr2:172877845-172878279	HepG2	liver:	n/a	chr2:172878075-172878086 chr2:172878075-172878086 chr2:172878076-172878085
39	ELF1	chr2:172877901-172878146	K562	blood:	n/a	chr2:172878075-172878086 chr2:172878075-172878086 chr2:172878076-172878085
40	ELF1	chr2:172877900-172878213	HepG2	liver:	n/a	chr2:172878075-172878086 chr2:172878075-172878086 chr2:172878076-172878085
41	ELF1	chr2:172877968-172878341	GM12878	blood:	n/a	chr2:172878075-172878086 chr2:172878075-172878086 chr2:172878076-172878085
42	EP300	chr2:172876732-172877062	GM12878	blood:	n/a	n/a
43	EP300	chr2:172878413-172878691	GM12878	blood:	n/a	n/a
44	EP300	chr2:172873611-172873986	Hela-S3	cervix:	n/a	n/a
45	EP300	chr2:172878454-172878695	GM12878	blood:	n/a	n/a
46	EP300	chr2:172876787-172877001	GM12878	blood:	n/a	n/a
47	ESR1	chr2:172877913-172878126	T-47D	breast:	n/a	chr2:172878023-172878040
48	ESR1	chr2:172877852-172878205	T-47D	breast:	n/a	chr2:172878023-172878040
49	ESR1	chr2:172873674-172873928	ECC-1	luminal epithelium:	n/a	n/a
50	ESR1	chr2:172877535-172878313	ECC-1	luminal epithelium:	n/a	chr2:172878023-172878040

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:172878103-172878153	ProgFib	skin:	n/a
2	chr2:172878103-172878153	HCPEpiC	choroid plexus:	n/a
3	chr2:172878103-172878153	T-47D	breast:	n/a
4	chr2:172878103-172878153	HRCEpiC	kidney:	n/a
5	chr2:172878103-172878153	SK-N-MC	brain:	n/a
6	chr2:172878103-172878153	RPTEC	kidney:	n/a
7	chr2:172878103-172878153	SKMC	muscle:	n/a
8	chr2:172878103-172878153	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:172878103-172878153	Hepatocyte	liver:	n/a
10	chr2:172878103-172878153	ECC-1	luminal epithelium:	n/a
11	chr2:172878103-172878153	A549	lung:	n/a
12	chr2:172878103-172878153	HEK293	kidney:	embryo
13	chr2:172878103-172878153	SK-N-SH_RA	brain:	n/a
14	chr2:172878103-172878153	GM12878	blood:	n/a
15	chr2:172878103-172878153	AG10803	skin:	n/a
16	chr2:172878103-172878153	AoSMC	blood vessel:	n/a
17	chr2:172878103-172878153	HEEpiC	esophagus:	n/a
18	chr2:172878103-172878153	GM12892	blood:	n/a
19	chr2:172878103-172878153	AG04449	skin:	fetal
20	chr2:172878103-172878153	MCF-7	breast:	n/a
21	chr2:172878103-172878153	SAEC	small airway:	n/a
22	chr2:172878103-172878153	H1-hESC	embryonic stem cell:	embryo
23	chr2:172878103-172878153	NH-A	brain:	n/a
24	chr2:172878103-172878153	LNCaP	prostate:	n/a
25	chr2:172878103-172878153	BE2_C	brain:	n/a
26	chr2:172878103-172878153	HRE	kidney:	n/a
27	chr2:172878103-172878153	AG09309	skin:	n/a
28	chr2:172878103-172878153	BJ	skin:	n/a
29	chr2:172878103-172878153	AG04450	lung:	fetal
30	chr2:172878103-172878153	IMR90	lung:	fetal
31	chr2:172878103-172878153	HIPEpiC	eye:	n/a
32	chr2:172878103-172878153	HMEC	breast:	n/a
33	chr2:172878103-172878153	HRPEpiC	eye:	n/a
34	chr2:172878103-172878153	AG09319	gingival:	n/a
35	chr2:172878103-172878153	GM19239	blood:	n/a
36	chr2:172878103-172878153	PANC-1	pancreas:	n/a
37	chr2:172878103-172878153	HL-60	blood:	n/a
38	chr2:172878103-172878153	MCF10A-Er-Src	breast:	n/a
39	chr2:172878103-172878153	HUVEC	blood vessel:	n/a
40	chr2:172878103-172878153	PFSK-1	brain:	n/a
41	chr2:172878103-172878153	HCT-116	colon:	n/a
42	chr2:172878103-172878153	NHDF-neo	bronchial:	n/a
43	chr2:172878103-172878153	HAEpiC	amniotic membrane:	n/a
44	chr2:172878103-172878153	Caco-2	colon:	n/a
45	chr2:172878103-172878153	HCM	heart:	n/a
46	chr2:172878103-172878153	NT2-D1	testis:	n/a
47	chr2:172878103-172878153	NB4	blood:	n/a
48	chr2:172878103-172878153	HNPCEpiC	eye:	n/a
49	chr2:172878103-172878153	GM06990	blood:	n/a
50	chr2:172878103-172878153	U87	brain:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:172870841..172873802-chr2:172876022..172878107,2	MCF-7	breast:
2	chr2:172872408..172874494-chr2:172948737..172950969,2	MCF-7	breast:
3	chr2:172749558..172752378-chr2:172870357..172872482,2	K562	blood:
4	chr2:172871676..172873421-chr2:172883167..172884730,2	K562	blood:
5	chr2:172872334..172876033-chr2:172959738..172961363,3	MCF-7	breast:
6	chr2:172869928..172872436-chr2:172950140..172951979,2	MCF-7	breast:
7	chr2:172865192..172866696-chr2:172882365..172884619,2	K562	blood:
8	chr2:172870841..172873802-chr2:172876022..172878107,2	MCF-7	breast:
9	chr2:172859788..172868192-chr2:172944876..172951443,18	MCF-7	breast:
10	chr2:172881211..172884149-chr2:172956604..172958164,2	K562	blood:
11	chr2:172864725..172866652-chr2:172872084..172875231,3	MCF-7	breast:
12	chr2:172873033..172874674-chr2:172958655..172960495,2	MCF-7	breast:
13	chr2:172866585..172869561-chr2:172915980..172919427,3	K562	blood:
14	chr2:172872941..172875027-chr2:172948561..172950206,2	MCF-7	breast:
15	chr2:172864480..172870614-chr2:172875986..172878962,8	K562	blood:
16	chr2:172859639..172861224-chr2:172868661..172870553,2	MCF-7	breast:
17	chr2:172863189..172870519-chr2:172946500..172952655,22	K562	blood:
18	chr2:172872308..172874513-chr2:172883342..172886066,2	MCF-7	breast:
19	chr2:172877706..172879734-chr2:172884622..172888221,3	K562	blood:
20	chr2:172882349..172884255-chr2:172963176..172965606,2	K562	blood:
21	chr2:172875864..172877390-chr2:172966146..172968015,2	MCF-7	breast:
22	chr2:172864500..172866706-chr2:172879081..172880840,2	K562	blood:
23	chr2:172872127..172874571-chr2:172915848..172917626,2	MCF-7	breast:
24	chr2:172872328..172874870-chr2:172965765..172968527,2	MCF-7	breast:
25	chr2:172867998..172870491-chr2:172948122..172949809,2	MCF-7	breast:
26	chr2:172747937..172750894-chr2:172866713..172868813,2	K562	blood:
27	chr2:172874695..172877681-chr2:172884146..172886439,2	K562	blood:
28	chr2:172862481..172869340-chr2:172872333..172878575,9	MCF-7	breast:
29	chr2:172860017..172861984-chr2:172875793..172878198,2	K562	blood:
30	chr2:172867339..172869674-chr2:172948065..172950386,2	K562	blood:
31	chr2:172878645..172880573-chr2:172892398..172894603,2	K562	blood:
32	chr2:172872308..172874513-chr2:172883342..172886066,2	MCF-7	breast:
33	chr2:172866585..172869561-chr2:172917120..172919427,2	K562	blood:
34	chr2:172880890..172883813-chr2:172885436..172887540,3	K562	blood:
35	chr2:172875314..172877741-chr2:172963379..172965447,2	MCF-7	breast:
36	chr2:172874695..172877681-chr2:172884146..172886439,2	K562	blood:
37	chr2:172862808..172868920-chr2:172961807..172971063,13	K562	blood:
38	chr2:172880544..172883813-chr2:172885436..172889250,4	K562	blood:
39	chr2:172857904..172859439-chr2:172876035..172878668,2	K562	blood:
40	chr2:172872086..172874566-chr2:172886607..172888423,2	MCF-7	breast:
41	chr2:172866012..172868252-chr2:172888365..172889925,2	K562	blood:
42	chr2:172867067..172870652-chr2:172884225..172887785,3	K562	blood:
43	chr2:172863436..172866210-chr2:172867525..172870127,5	MCF-7	breast:
44	chr2:172881886..172883494-chr2:172885101..172888939,4	MCF-7	breast:
45	chr2:172871676..172873421-chr2:172883167..172884730,2	K562	blood:
46	chr2:172836942..172840182-chr2:172865086..172867545,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METAP1D-2	chr2:172874105-172874190	l_1987_chr2:172825346-172897114_testes

No data

Variant related genes	Relation type
METAP1D	TF binding region
SLC25A12	TF binding region
METAP1D	CpG island
SLC25A12	CpG island
ENSG00000172878	chromatin interactions
ENSG00000115840	chromatin interactions
ENSG00000115844	chromatin interactions
ENSG00000144355	chromatin interactions
ENSG00000236651	chromatin interactions

Extended variants
information (count: 583 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62183801	chr2:172867475-172867476	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183261262	chr2:172867476-172867477	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs529657707	chr2:172867543-172867544	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs370450413	chr2:172867560-172867561	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs188723526	chr2:172867580-172867581	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs375166357	chr2:172867603-172867604	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs548410223	chr2:172867609-172867610	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs193046971	chr2:172867635-172867636	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs562589403	chr2:172867715-172867716	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs183161592	chr2:172867760-172867761	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs571002203	chr2:172867780-172867781	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs187892582	chr2:172867786-172867787	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs75990149	chr2:172867796-172867797	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs574753027	chr2:172867810-172867811	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs544910413	chr2:172867815-172867816	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs533315017	chr2:172867821-172867822	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs191238894	chr2:172867826-172867827	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs73976543	chr2:172867852-172867853	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs147866719	chr2:172867993-172867994	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs148955922	chr2:172868091-172868092	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs532111864	chr2:172868133-172868134	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs183790573	chr2:172868138-172868139	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs562217294	chr2:172868228-172868229	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs529662733	chr2:172868289-172868290	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs142869918	chr2:172868316-172868317	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs79609957	chr2:172868393-172868394	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs566695837	chr2:172868418-172868419	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs371754435	chr2:172868440-172868441	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs150994726	chr2:172868464-172868465	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs545220158	chr2:172868541-172868542	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs560578968	chr2:172868557-172868558	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs62183802	chr2:172868703-172868704	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376378585	chr2:172868704-172868705	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs189375812	chr2:172868717-172868718	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs541969409	chr2:172868721-172868722	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs556714035	chr2:172868735-172868736	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs192927489	chr2:172868737-172868738	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs535491481	chr2:172868748-172868749	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs113581406	chr2:172868752-172868753	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs185023622	chr2:172868765-172868766	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs572695596	chr2:172868787-172868788	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs190314812	chr2:172868807-172868808	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs181717777	chr2:172868818-172868819	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs576251933	chr2:172868887-172868888	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs140821192	chr2:172868920-172868921	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs114288600	chr2:172868990-172868991	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs569502549	chr2:172869036-172869037	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs541509729	chr2:172869061-172869062	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs368378892	chr2:172869120-172869121	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs186420198	chr2:172869153-172869154	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	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
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	21384125	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172865200-172886600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:172865400-172877200	Weak transcription	Pancreas	Pancrea
3	chr2:172865400-172878000	Weak transcription	Gastric	stomach
4	chr2:172865600-172869600	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr2:172865600-172870400	Weak transcription	Right Ventricle	heart
6	chr2:172865600-172875200	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr2:172865600-172876600	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr2:172865600-172877200	Weak transcription	Psoas Muscle	Psoas
9	chr2:172865600-172878000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr2:172865600-172897400	Weak transcription	Primary T cells from cord blood	blood
11	chr2:172865800-172869000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr2:172865800-172869800	Weak transcription	Brain Anterior Caudate	brain
13	chr2:172865800-172876600	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr2:172865800-172877200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr2:172865800-172877600	Weak transcription	Fetal Kidney	kidney
16	chr2:172865800-172878000	Weak transcription	Primary B cells from cord blood	blood
17	chr2:172865800-172886400	Weak transcription	Fetal Intestine Small	intestine
18	chr2:172865800-172886600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr2:172866000-172868800	Weak transcription	Stomach Mucosa	stomach
20	chr2:172866000-172872600	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr2:172866000-172873600	Weak transcription	Fetal Lung	lung
22	chr2:172866000-172876400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr2:172866000-172877200	Weak transcription	Ovary	ovary
24	chr2:172866000-172877600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr2:172866000-172877800	Weak transcription	HSMM	muscle
26	chr2:172866000-172878000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr2:172866000-172886800	Weak transcription	HSMMtube	muscle
28	chr2:172866200-172876400	Weak transcription	Dnd41	blood
29	chr2:172866200-172877000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:172866400-172875800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr2:172866800-172882600	Weak transcription	K562	blood
32	chr2:172867400-172867600	Enhancers	Brain Germinal Matrix	brain
33	chr2:172869400-172869600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:172869600-172870000	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr2:172869600-172877200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr2:172870000-172875400	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr2:172872000-172873800	Enhancers	HepG2	liver
38	chr2:172873000-172875000	Enhancers	HMEC	breast
39	chr2:172873200-172874600	Enhancers	A549	lung
40	chr2:172873200-172875000	Enhancers	NHEK	skin
41	chr2:172873400-172873600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr2:172873400-172875000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr2:172873600-172874000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr2:172873600-172874000	Enhancers	NHLF	lung
45	chr2:172873600-172874200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr2:172873600-172874400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:172873600-172874800	Enhancers	Hela-S3	cervix
48	chr2:172873800-172874000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:172873800-172877200	Weak transcription	HepG2	liver
50	chr2:172874000-172877800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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