Variant report

Variant	nsv584668
Chromosome Location	chr2:231178876-231258450
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1012)
CpG islands
(count:427)
Chromatin interactive
region (count:41)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:231193785-231193842	K562	blood:	n/a	n/a
2	ARID3A	chr2:231195481-231195828	K562	blood:	n/a	n/a
3	ARID3A	chr2:231200089-231200926	K562	blood:	n/a	n/a
4	ARID3A	chr2:231220790-231221227	HepG2	liver:	n/a	n/a
5	ATF1	chr2:231200164-231200933	K562	blood:	n/a	n/a
6	ATF1	chr2:231195509-231195828	K562	blood:	n/a	n/a
7	ATF2	chr2:231183218-231184347	GM12878	blood:	n/a	n/a
8	ATF2	chr2:231212671-231213120	GM12878	blood:	n/a	n/a
9	ATF2	chr2:231191449-231192490	GM12878	blood:	n/a	n/a
10	ATF2	chr2:231212653-231213056	GM12878	blood:	n/a	n/a
11	ATF2	chr2:231191499-231192552	GM12878	blood:	n/a	n/a
12	ATF3	chr2:231187989-231188190	K562	blood:	n/a	n/a
13	ATF3	chr2:231191653-231192040	K562	blood:	n/a	n/a
14	ATF3	chr2:231195446-231195770	K562	blood:	n/a	n/a
15	BACH1	chr2:231212939-231212941	K562	blood:	n/a	n/a
16	BACH1	chr2:231195688-231195715	K562	blood:	n/a	n/a
17	BACH1	chr2:231246869-231247136	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr2:231183939-231184211	GM12878	blood:	n/a	n/a
19	BATF	chr2:231191613-231192080	GM12878	blood:	n/a	chr2:231191862-231191873
20	BATF	chr2:231192119-231192378	GM12878	blood:	n/a	n/a
21	BATF	chr2:231212698-231213095	GM12878	blood:	n/a	n/a
22	BATF	chr2:231223054-231223350	GM12878	blood:	n/a	chr2:231223160-231223171
23	BATF	chr2:231212475-231213126	GM12878	blood:	n/a	n/a
24	BCL11A	chr2:231183914-231184198	GM12878	blood:	n/a	n/a
25	BCL11A	chr2:231212720-231213098	GM12878	blood:	n/a	n/a
26	BCL3	chr2:231183905-231184420	GM12878	blood:	n/a	n/a
27	BCLAF1	chr2:231191490-231192616	GM12878	blood:	n/a	n/a
28	BCLAF1	chr2:231183804-231184388	GM12878	blood:	n/a	n/a
29	BCLAF1	chr2:231183163-231183628	GM12878	blood:	n/a	n/a
30	BHLHE40	chr2:231187972-231188245	K562	blood:	n/a	n/a
31	BHLHE40	chr2:231195575-231195864	K562	blood:	n/a	n/a
32	BHLHE40	chr2:231191722-231192202	GM12878	blood:	n/a	n/a
33	BHLHE40	chr2:231183871-231184059	GM12878	blood:	n/a	n/a
34	BHLHE40	chr2:231191646-231192075	K562	blood:	n/a	n/a
35	BHLHE40	chr2:231200051-231200459	K562	blood:	n/a	n/a
36	BHLHE40	chr2:231212896-231213138	GM12878	blood:	n/a	n/a
37	BRCA1	chr2:231188205-231188381	HepG2	liver:	n/a	n/a
38	CBX3	chr2:231191548-231192096	K562	blood:	n/a	n/a
39	CBX3	chr2:231195454-231195813	K562	blood:	n/a	n/a
40	CBX3	chr2:231206580-231206982	K562	blood:	n/a	n/a
41	CBX3	chr2:231187908-231188441	K562	blood:	n/a	n/a
42	CBX3	chr2:231211141-231211548	K562	blood:	n/a	n/a
43	CBX3	chr2:231187268-231187635	K562	blood:	n/a	n/a
44	CBX3	chr2:231207951-231208212	K562	blood:	n/a	n/a
45	CEBPB	chr2:231220796-231221121	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:231220809-231221187	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:231191419-231191718	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:231191464-231191951	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:231193781-231193938	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:231181559-231181877	HepG2	liver:	n/a	chr2:231181723-231181734

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:231190414-231190464	HEEpiC	esophagus:	n/a
2	chr2:231191662-231191712	HEK293	kidney:	embryo
3	chr2:231191916-231191966	MCF10A-Er-Src	breast:	n/a
4	chr2:231191893-231191943	HIPEpiC	eye:	n/a
5	chr2:231235574-231235624	AG09309	skin:	n/a
6	chr2:231191662-231191712	SK-N-SH_RA	brain:	n/a
7	chr2:231191893-231191943	HRCEpiC	kidney:	n/a
8	chr2:231191916-231191966	GM12878	blood:	n/a
9	chr2:231190414-231190464	AG09319	gingival:	n/a
10	chr2:231191662-231191712	AG09309	skin:	n/a
11	chr2:231190414-231190464	HCF	heart:	n/a
12	chr2:231191727-231191777	ProgFib	skin:	n/a
13	chr2:231191916-231191966	NT2-D1	testis:	n/a
14	chr2:231191893-231191943	GM06990	blood:	n/a
15	chr2:231191876-231191926	NB4	blood:	n/a
16	chr2:231191662-231191712	AG04449	skin:	fetal
17	chr2:231191727-231191777	HepG2	liver:	n/a
18	chr2:231191662-231191712	H1-hESC	embryonic stem cell:	embryo
19	chr2:231191662-231191712	HRCEpiC	kidney:	n/a
20	chr2:231190414-231190464	AG04450	lung:	fetal
21	chr2:231235574-231235624	U87	brain:	n/a
22	chr2:231191662-231191712	NHDF-neo	bronchial:	n/a
23	chr2:231191876-231191926	SK-N-SH_RA	brain:	n/a
24	chr2:231191876-231191926	AoSMC	blood vessel:	n/a
25	chr2:231191916-231191966	Caco-2	colon:	n/a
26	chr2:231191876-231191926	AG04449	skin:	fetal
27	chr2:231191662-231191712	PFSK-1	brain:	n/a
28	chr2:231235574-231235624	HIPEpiC	eye:	n/a
29	chr2:231191893-231191943	SK-N-SH	brain:	n/a
30	chr2:231191876-231191926	PrEC	prostate:	n/a
31	chr2:231191916-231191966	GM19239	blood:	n/a
32	chr2:231190414-231190464	HRCEpiC	kidney:	n/a
33	chr2:231235574-231235624	GM12892	blood:	n/a
34	chr2:231191893-231191943	SK-N-MC	brain:	n/a
35	chr2:231191893-231191943	PFSK-1	brain:	n/a
36	chr2:231235574-231235624	SK-N-SH	brain:	n/a
37	chr2:231191727-231191777	MCF10A-Er-Src	breast:	n/a
38	chr2:231191893-231191943	CMK	blood:	n/a
39	chr2:231191916-231191966	LNCaP	prostate:	n/a
40	chr2:231191662-231191712	HMEC	breast:	n/a
41	chr2:231190414-231190464	H1-hESC	embryonic stem cell:	embryo
42	chr2:231191662-231191712	Hepatocyte	liver:	n/a
43	chr2:231191727-231191777	A549	lung:	n/a
44	chr2:231190414-231190464	K562	blood:	n/a
45	chr2:231191727-231191777	ECC-1	luminal epithelium:	n/a
46	chr2:231191662-231191712	SKMC	muscle:	n/a
47	chr2:231191916-231191966	HRPEpiC	eye:	n/a
48	chr2:231191727-231191777	LNCaP	prostate:	n/a
49	chr2:231191893-231191943	K562	blood:	n/a
50	chr2:231190414-231190464	A549	lung:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:231235932..231237817-chr2:231243056..231245722,2	K562	blood:
2	chr2:231183815..231186331-chr2:231189683..231191890,3	MCF-7	breast:
3	chr2:231211608..231214034-chr2:231214766..231217419,2	K562	blood:
4	chr2:231232811..231234963-chr2:231243502..231245395,2	K562	blood:
5	chr2:231191663..231192385-chr2:231280228..231281288,3	Hela-S3	cervix:
6	chr2:231191754..231192275-chr2:231280477..231281313,4	HCT-116	colon:
7	chr2:231235932..231237817-chr2:231243056..231245722,2	K562	blood:
8	chr2:231191400..231192273-chr2:231280039..231281003,2	MCF-7	breast:
9	chr2:231187795..231189523-chr2:231196681..231199404,2	MCF-7	breast:
10	chr2:231187646..231188478-chr2:231276184..231277085,2	HCT-116	colon:
11	chr2:231187675..231188630-chr2:231663234..231663815,2	K562	blood:
12	chr2:231194037..231196548-chr2:231226140..231228040,2	K562	blood:
13	chr2:231211208..231214034-chr2:231215264..231217419,2	K562	blood:
14	chr2:231187450..231190323-chr2:231192038..231194221,2	K562	blood:
15	chr2:231250673..231252951-chr2:231254109..231256319,2	K562	blood:
16	chr2:231245270..231247001-chr2:231250596..231253585,2	K562	blood:
17	chr2:231250673..231252951-chr2:231254109..231256319,2	K562	blood:
18	chr2:231225373..231227509-chr2:231238018..231240508,2	MCF-7	breast:
19	chr2:231195214..231197850-chr2:231199409..231202103,3	K562	blood:
20	chr2:231211181..231213107-chr2:231272080..231274624,2	K562	blood:
21	chr2:231211208..231214034-chr2:231215264..231217419,2	K562	blood:
22	chr2:231182687..231184963-chr2:231663131..231665649,2	K562	blood:
23	chr2:231208083..231209786-chr2:231217678..231219607,2	K562	blood:
24	chr2:231177190..231178996-chr2:231181299..231183714,2	K562	blood:
25	chr2:231250470..231252017-chr2:231286033..231287832,2	K562	blood:
26	chr2:231211608..231214034-chr2:231214766..231217419,2	K562	blood:
27	chr2:231177190..231178996-chr2:231181299..231183714,2	K562	blood:
28	chr2:231176097..231178034-chr2:231181270..231184101,2	MCF-7	breast:
29	chr2:231192831..231194646-chr2:231195490..231197463,2	K562	blood:
30	chr2:231232811..231234963-chr2:231243502..231245395,2	K562	blood:
31	chr2:231199506..231201405-chr2:231206253..231208187,2	K562	blood:
32	chr2:231225373..231227509-chr2:231238018..231240508,2	MCF-7	breast:
33	chr2:231192831..231194646-chr2:231195490..231197463,2	K562	blood:
34	chr2:231195214..231197850-chr2:231199409..231202103,3	K562	blood:
35	chr2:231208083..231209786-chr2:231217678..231219607,2	K562	blood:
36	chr2:231187795..231189523-chr2:231196681..231199404,2	MCF-7	breast:
37	chr16:17916509..17917287-chr2:231255356..231256048,2	MCF-7	breast:
38	chr2:231245270..231247001-chr2:231250596..231253585,2	K562	blood:
39	chr2:231194037..231196548-chr2:231226140..231228040,2	K562	blood:
40	chr2:231187450..231190323-chr2:231192038..231194221,2	K562	blood:
41	chr2:231183815..231186331-chr2:231189683..231191890,3	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SP140-5	chr2:231258129-231258176	NONHSAT077278
2	lnc-SP140-5	chr2:231258129-231258176	NONHSAT077280
3	lnc-SP140-5	chr2:231253274-231253348	NONHSAT077278
4	lnc-SP140-5	chr2:231249956-231250019	NONHSAT077279
5	lnc-SP140-5	chr2:231254634-231254738	NONHSAT077278
6	lnc-SP140-5	chr2:231256802-231256944	NONHSAT077278
7	lnc-SP140-5	chr2:231256802-231256944	NONHSAT077280
8	lnc-SP140-5	chr2:231236313-231236366	NONHSAT077278
9	lnc-SP140-5	chr2:231249939-231250019	NONHSAT077278
10	lnc-SP140-5	chr2:231256430-231256522	NONHSAT077280
11	lnc-SP140-5	chr2:231248225-231248290	NONHSAT077278
12	lnc-SP140-5	chr2:231235621-231235682	NONHSAT077278
13	lnc-SP140-5	chr2:231253274-231253501	NONHSAT077279

No data

Variant related genes	Relation type
SP140L	TF binding region
SP140L	CpG island
ENSG00000067066	chromatin interactions
ENSG00000185404	chromatin interactions

Extended variants
information (count: 3018 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3018 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs730010	chr2:231178876-231178877	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574053551	chr2:231178931-231178932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541495935	chr2:231178983-231178984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573923107	chr2:231179006-231179007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141306969	chr2:231179021-231179022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183441740	chr2:231179052-231179053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533413516	chr2:231179079-231179080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150826133	chr2:231179136-231179137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189015506	chr2:231179148-231179149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138295565	chr2:231179159-231179160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549337038	chr2:231179174-231179175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567803697	chr2:231179181-231179182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528185667	chr2:231179302-231179303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546331152	chr2:231179325-231179326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570986273	chr2:231179375-231179376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538279635	chr2:231179376-231179377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556879124	chr2:231179435-231179436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569076943	chr2:231179442-231179443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536499913	chr2:231179455-231179456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs933956	chr2:231179460-231179461	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs573114259	chr2:231179484-231179485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533971128	chr2:231179559-231179560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2396743	chr2:231179590-231179591	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs578133898	chr2:231179611-231179612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77926108	chr2:231179628-231179629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114417125	chr2:231179661-231179662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192921694	chr2:231179669-231179670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs55798848	chr2:231179767-231179768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543871689	chr2:231179822-231179823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558316685	chr2:231179827-231179828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543266666	chr2:231179832-231179833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185171763	chr2:231179835-231179836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189647481	chr2:231179871-231179872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147266034	chr2:231179877-231179878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6731421	chr2:231179884-231179885	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564651770	chr2:231179900-231179901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563552837	chr2:231179925-231179926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532048817	chr2:231179932-231179933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12615773	chr2:231179955-231179956	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs191896290	chr2:231179983-231179984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370580577	chr2:231180009-231180010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184086482	chr2:231180018-231180019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546087719	chr2:231180027-231180028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140785095	chr2:231180059-231180060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558750975	chr2:231180138-231180139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs578159493	chr2:231180146-231180147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373009438	chr2:231180151-231180152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56017039	chr2:231180161-231180162	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs557090063	chr2:231180229-231180230	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543511655	chr2:231180233-231180234	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1952 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231147800-231182400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr2:231153800-231183400	Weak transcription	Duodenum Mucosa	Duodenum
3	chr2:231162600-231180800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr2:231165400-231180200	Weak transcription	Primary T cells from cord blood	blood
5	chr2:231165400-231181600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr2:231165800-231181000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr2:231172400-231180800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr2:231174200-231179600	Strong transcription	Primary T helper cells PMA-I stimulated	--
9	chr2:231174400-231182000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:231175000-231183800	Weak transcription	HMEC	breast
11	chr2:231175400-231180200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr2:231175400-231182000	Weak transcription	Lung	lung
13	chr2:231176000-231181000	Strong transcription	Primary B cells from peripheral blood	blood
14	chr2:231176800-231179000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr2:231177200-231179200	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr2:231177200-231179800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr2:231177200-231180400	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr2:231177400-231179400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr2:231177400-231182000	Strong transcription	Primary B cells from cord blood	blood
20	chr2:231177800-231181800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:231177800-231182000	Weak transcription	Spleen	Spleen
22	chr2:231178200-231180800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr2:231178800-231181600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr2:231178800-231182000	Weak transcription	GM12878-XiMat	blood
25	chr2:231179000-231181800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr2:231179200-231180800	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr2:231179600-231180600	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr2:231179800-231182400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr2:231180200-231182200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr2:231180200-231183000	Enhancers	Primary T cells from cord blood	blood
31	chr2:231180400-231181400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr2:231180600-231182800	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr2:231180800-231182200	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr2:231180800-231182600	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr2:231180800-231182600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr2:231180800-231183600	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr2:231181000-231182600	Genic enhancers	Primary B cells from peripheral blood	blood
38	chr2:231181000-231183400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr2:231181400-231181800	Enhancers	Primary T cells fromperipheralblood	blood
40	chr2:231181600-231183200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr2:231181600-231183200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr2:231181800-231182600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:231181800-231182600	Genic enhancers	Primary T cells fromperipheralblood	blood
44	chr2:231181800-231183400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr2:231182000-231182200	Enhancers	Right Atrium	heart
46	chr2:231182000-231182400	Genic enhancers	Primary B cells from cord blood	blood
47	chr2:231182000-231182400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr2:231182000-231182400	Enhancers	Lung	lung
49	chr2:231182000-231182400	Enhancers	Spleen	Spleen
50	chr2:231182000-231182800	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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