Variant report

Variant	nsv873618
Chromosome Location	chr2:9870631-9919759
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1782)
CpG islands
(count:549)
Chromatin interactive
region (count:101)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1782 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:9903798-9904137	K562	blood:	n/a	n/a
2	ARID3A	chr2:9905759-9906088	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:9908684-9908853	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:9910531-9910839	K562	blood:	n/a	n/a
5	ARID3A	chr2:9893333-9893592	K562	blood:	n/a	n/a
6	ATF1	chr2:9900214-9900455	K562	blood:	n/a	n/a
7	ATF1	chr2:9903764-9904095	K562	blood:	n/a	n/a
8	ATF2	chr2:9892636-9893134	GM12878	blood:	n/a	n/a
9	ATF2	chr2:9893195-9893756	GM12878	blood:	n/a	n/a
10	ATF2	chr2:9888714-9889291	GM12878	blood:	n/a	n/a
11	ATF2	chr2:9893214-9893700	GM12878	blood:	n/a	n/a
12	ATF3	chr2:9900151-9900484	K562	blood:	n/a	n/a
13	ATF3	chr2:9903763-9904096	K562	blood:	n/a	n/a
14	BACH1	chr2:9903801-9904037	K562	blood:	n/a	n/a
15	BACH1	chr2:9909590-9909840	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr2:9908684-9908919	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr2:9893245-9893716	GM12878	blood:	n/a	chr2:9893467-9893478
18	BATF	chr2:9894384-9894701	GM12878	blood:	n/a	n/a
19	BATF	chr2:9878679-9879016	GM12878	blood:	n/a	n/a
20	BATF	chr2:9894355-9894756	GM12878	blood:	n/a	n/a
21	BATF	chr2:9904505-9904797	GM12878	blood:	n/a	n/a
22	BATF	chr2:9892661-9893121	GM12878	blood:	n/a	chr2:9892919-9892929
23	BATF	chr2:9888898-9889202	GM12878	blood:	n/a	n/a
24	BATF	chr2:9893229-9893775	GM12878	blood:	n/a	chr2:9893467-9893478
25	BCL11A	chr2:9892734-9893001	GM12878	blood:	n/a	n/a
26	BCL11A	chr2:9894435-9894704	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:9893336-9893728	GM12878	blood:	n/a	chr2:9893680-9893689 chr2:9893462-9893471
28	BCL11A	chr2:9893330-9893647	GM12878	blood:	n/a	chr2:9893462-9893471
29	BCL3	chr2:9888749-9889158	GM12878	blood:	n/a	chr2:9889030-9889039
30	BCL3	chr2:9905927-9906348	GM12878	blood:	n/a	n/a
31	BCL3	chr2:9903767-9904068	GM12878	blood:	n/a	n/a
32	BCL3	chr2:9892544-9893897	A549	lung:	n/a	chr2:9893680-9893689 chr2:9893462-9893471
33	BCL3	chr2:9893294-9893744	GM12878	blood:	n/a	chr2:9893680-9893689 chr2:9893462-9893471
34	BCLAF1	chr2:9893172-9893750	GM12878	blood:	n/a	chr2:9893680-9893689 chr2:9893462-9893471
35	BCLAF1	chr2:9888734-9889132	GM12878	blood:	n/a	chr2:9889030-9889039
36	BHLHE40	chr2:9892878-9893025	K562	blood:	n/a	n/a
37	BHLHE40	chr2:9893245-9893765	K562	blood:	n/a	n/a
38	BHLHE40	chr2:9894360-9894794	GM12878	blood:	n/a	n/a
39	BHLHE40	chr2:9916503-9916711	K562	blood:	n/a	n/a
40	BHLHE40	chr2:9909551-9909846	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:9893321-9893742	GM12878	blood:	n/a	n/a
42	BHLHE40	chr2:9910393-9910909	K562	blood:	n/a	chr2:9910532-9910548 chr2:9910630-9910646
43	BHLHE40	chr2:9908205-9908223	GM12878	blood:	n/a	n/a
44	BHLHE40	chr2:9909587-9909709	K562	blood:	n/a	n/a
45	BHLHE40	chr2:9901609-9901903	K562	blood:	n/a	n/a
46	BHLHE40	chr2:9908709-9908913	K562	blood:	n/a	n/a
47	BHLHE40	chr2:9878527-9878675	GM12878	blood:	n/a	n/a
48	BHLHE40	chr2:9918124-9918503	HepG2	liver:	n/a	n/a
49	BHLHE40	chr2:9905808-9905961	K562	blood:	n/a	n/a
50	BHLHE40	chr2:9918138-9918487	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:9908576-9908626	NH-A	brain:	n/a
2	chr2:9919440-9919490	SAEC	small airway:	n/a
3	chr2:9894165-9894215	NT2-D1	testis:	n/a
4	chr2:9894335-9894385	Hepatocyte	liver:	n/a
5	chr2:9911124-9911174	HCT-116	colon:	n/a
6	chr2:9911124-9911174	SK-N-SH_RA	brain:	n/a
7	chr2:9894165-9894215	HUVEC	blood vessel:	n/a
8	chr2:9919440-9919490	HEK293	kidney:	embryo
9	chr2:9911124-9911174	AG09319	gingival:	n/a
10	chr2:9878816-9878866	HCF	heart:	n/a
11	chr2:9919494-9919544	NB4	blood:	n/a
12	chr2:9908576-9908626	NHBE	bronchial:	n/a
13	chr2:9878816-9878866	HUVEC	blood vessel:	n/a
14	chr2:9878816-9878866	MCF-7	breast:	n/a
15	chr2:9919440-9919490	HepG2	liver:	n/a
16	chr2:9893528-9893578	ProgFib	skin:	n/a
17	chr2:9898228-9898278	PFSK-1	brain:	n/a
18	chr2:9919494-9919544	Jurkat	blood:	n/a
19	chr2:9878816-9878866	PrEC	prostate:	n/a
20	chr2:9893528-9893578	MCF10A-Er-Src	breast:	n/a
21	chr2:9919440-9919490	ProgFib	skin:	n/a
22	chr2:9894165-9894215	SK-N-MC	brain:	n/a
23	chr2:9908576-9908626	HEK293	kidney:	embryo
24	chr2:9898228-9898278	NHDF-neo	bronchial:	n/a
25	chr2:9898228-9898278	MCF10A-Er-Src	breast:	n/a
26	chr2:9919440-9919490	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:9919494-9919544	HRE	kidney:	n/a
28	chr2:9894335-9894385	Hela-S3	cervix:	n/a
29	chr2:9919494-9919544	HEK293	kidney:	embryo
30	chr2:9894335-9894385	AG04450	lung:	fetal
31	chr2:9898228-9898278	ECC-1	luminal epithelium:	n/a
32	chr2:9893528-9893578	GM06990	blood:	n/a
33	chr2:9893528-9893578	HEK293	kidney:	embryo
34	chr2:9894165-9894215	A549	lung:	n/a
35	chr2:9894335-9894385	HRPEpiC	eye:	n/a
36	chr2:9919440-9919490	HL-60	blood:	n/a
37	chr2:9893528-9893578	CMK	blood:	n/a
38	chr2:9908576-9908626	AG09309	skin:	n/a
39	chr2:9919494-9919544	HL-60	blood:	n/a
40	chr2:9878816-9878866	AG09309	skin:	n/a
41	chr2:9894165-9894215	AG09309	skin:	n/a
42	chr2:9898228-9898278	NT2-D1	testis:	n/a
43	chr2:9919440-9919490	AG04450	lung:	fetal
44	chr2:9893528-9893578	ECC-1	luminal epithelium:	n/a
45	chr2:9894335-9894385	NB4	blood:	n/a
46	chr2:9893528-9893578	SAEC	small airway:	n/a
47	chr2:9878816-9878866	HRPEpiC	eye:	n/a
48	chr2:9908576-9908626	U87	brain:	n/a
49	chr2:9919440-9919490	NT2-D1	testis:	n/a
50	chr2:9894335-9894385	T-47D	breast:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:9877832..9879861-chr2:9884355..9886742,3	K562	blood:
2	chr2:9855761..9857318-chr2:9876058..9878208,2	K562	blood:
3	chr2:9899081..9899639-chr3:43902591..43903091,2	MCF-7	breast:
4	chr2:9787484..9789200-chr2:9888207..9889729,2	K562	blood:
5	chr2:9913973..9916043-chr2:9918215..9920682,2	K562	blood:
6	chr2:9694952..9697993-chr2:9876014..9878927,3	MCF-7	breast:
7	chr2:9893059..9895633-chr2:9899321..9902671,3	K562	blood:
8	chr2:9910622..9911180-chr2:10237098..10237720,2	K562	blood:
9	chr2:9769153..9773017-chr2:9899930..9902488,4	K562	blood:
10	chr2:9913973..9916043-chr2:9918215..9920682,2	K562	blood:
11	chr2:9904685..9905408-chr2:9918226..9918742,2	K562	blood:
12	chr2:9897337..9900295-chr2:9937034..9939837,3	K562	blood:
13	chr2:9910558..9913108-chr2:10185637..10189105,3	MCF-7	breast:
14	chr2:9897831..9899412-chr2:9902196..9904626,2	MCF-7	breast:
15	chr2:9888046..9890254-chr2:9893584..9895138,2	K562	blood:
16	chr2:9901947..9904351-chr2:9980319..9983166,2	K562	blood:
17	chr2:9912711..9914278-chr2:9916005..9917523,2	MCF-7	breast:
18	chr2:9911818..9914700-chr2:9914893..9917161,2	K562	blood:
19	chr2:9907009..9909399-chr2:10572837..10575430,2	K562	blood:
20	chr2:9892015..9895829-chr2:9904744..9907713,4	K562	blood:
21	chr2:9694937..9699400-chr2:9908606..9911252,4	K562	blood:
22	chr2:9891910..9893733-chr2:9895279..9898420,3	MCF-7	breast:
23	chr2:9772230..9774093-chr2:9892101..9894340,2	MCF-7	breast:
24	chr2:9887703..9890322-chr2:9895249..9898241,2	MCF-7	breast:
25	chr2:9843332..9845543-chr2:9887968..9890552,2	K562	blood:
26	chr2:9842465..9843983-chr2:9901077..9903005,2	K562	blood:
27	chr2:9888046..9890254-chr2:9893584..9895138,2	K562	blood:
28	chr2:9769198..9773144-chr2:9916945..9918889,4	MCF-7	breast:
29	chr2:9892798..9893661-chr3:149530498..149531325,2	Hela-S3	cervix:
30	chr2:9910788..9914069-chr2:9915018..9918206,3	K562	blood:
31	chr2:9877856..9880099-chr2:9889992..9892399,2	K562	blood:
32	chr2:9913973..9917175-chr2:9918406..9921250,3	K562	blood:
33	chr2:9769416..9771416-chr2:9887932..9889468,2	K562	blood:
34	chr2:9897830..9899713-chr2:9900837..9903744,2	K562	blood:
35	chr2:9871478..9874528-chr2:9876144..9879356,3	K562	blood:
36	chr2:9907890..9909492-chr2:9937494..9939085,2	MCF-7	breast:
37	chr2:9877832..9879411-chrX:76718203..76719726,2	K562	blood:
38	chr2:9910757..9913567-chr2:10174591..10176436,2	K562	blood:
39	chr2:9881645..9885042-chr2:9886477..9889282,3	K562	blood:
40	chr2:9870027..9872978-chr2:9873410..9875751,2	K562	blood:
41	chr1:245493743..245494253-chr2:9877159..9877996,2	MCF-7	breast:
42	chr2:9871478..9874528-chr2:9876144..9879356,3	K562	blood:
43	chr2:9892015..9894940-chr2:9904744..9907619,3	K562	blood:
44	chr2:9893434..9894306-chr6:31619956..31620466,2	Hela-S3	cervix:
45	chr10:92980146..92980794-chr2:9892579..9893415,2	Hela-S3	cervix:
46	chr2:9748514..9750852-chr2:9899112..9901012,2	K562	blood:
47	chr2:9851071..9852686-chr2:9893395..9896154,2	K562	blood:
48	chr2:9893534..9896583-chr2:9907885..9911717,3	K562	blood:
49	chr2:9911818..9914700-chr2:9914893..9917161,2	K562	blood:
50	chr2:9877856..9880099-chr2:9889992..9892399,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YWHAQ-1	chr2:9910328-9910470	XLOC_001982
2	lnc-YWHAQ-1	chr2:9897625-9899428	XLOC_001982

No data

Variant related genes	Relation type
ENSG00000240960	TF binding region
ENSG00000243491	TF binding region
RNU4-73P	TF binding region
ENSG00000240960	CpG island
ENSG00000243491	CpG island
RNU4-73P	CpG island
ENSG00000243491	chromatin interactions
ENSG00000180628	chromatin interactions
ENSG00000271855	chromatin interactions
ENSG00000115750	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000172059	chromatin interactions
ENSG00000151694	chromatin interactions
ENSG00000272524	chromatin interactions
ENSG00000082996	chromatin interactions
ENSG00000240960	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000260077	chromatin interactions
ENSG00000134308	chromatin interactions
ENSG00000171848	chromatin interactions

Extended variants
information (count: 2277 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2277 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7592044	chr2:9870631-9870632	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575287846	chr2:9870669-9870670	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548404590	chr2:9870693-9870694	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543905003	chr2:9870722-9870723	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568396221	chr2:9870726-9870727	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77401857	chr2:9870737-9870738	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373011025	chr2:9870749-9870750	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185253438	chr2:9870781-9870782	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570449892	chr2:9870786-9870787	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190896673	chr2:9870793-9870794	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73152972	chr2:9870796-9870797	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs572843778	chr2:9870805-9870806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561199225	chr2:9870854-9870855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs58577971	chr2:9870870-9870871	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs74171467	chr2:9870880-9870881	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs150484636	chr2:9870885-9870886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138361471	chr2:9870895-9870896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183967573	chr2:9870910-9870911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374512794	chr2:9870920-9870921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563955919	chr2:9870933-9870934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368634159	chr2:9870937-9870938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112934947	chr2:9870940-9870941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112607987	chr2:9870947-9870948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188866184	chr2:9870952-9870953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149249958	chr2:9870957-9870958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146190688	chr2:9870962-9870963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139180911	chr2:9870967-9870968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111238618	chr2:9870977-9870978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142498027	chr2:9870982-9870983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192919427	chr2:9871035-9871036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546415353	chr2:9871057-9871058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560230917	chr2:9871114-9871115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569243880	chr2:9871141-9871142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528682279	chr2:9871199-9871200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113531318	chr2:9871212-9871213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145999135	chr2:9871213-9871214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111841091	chr2:9871282-9871283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550591780	chr2:9871291-9871292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182849227	chr2:9871338-9871339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533099629	chr2:9871364-9871365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142197992	chr2:9871414-9871415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566613467	chr2:9871425-9871426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535309723	chr2:9871450-9871451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555403735	chr2:9871475-9871476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs70948837	chr2:9871488-9871489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs397983837	chr2:9871490-9871491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568894028	chr2:9871532-9871533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113302579	chr2:9871539-9871540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112183870	chr2:9871557-9871558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73155135	chr2:9871572-9871573	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9869600-9875800	Weak transcription	Fetal Thymus	thymus
2	chr2:9869800-9871200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:9870400-9870800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:9870400-9870800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr2:9870600-9870800	Enhancers	K562	blood
6	chr2:9871400-9871600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr2:9875000-9879200	Enhancers	Primary T cells fromperipheralblood	blood
8	chr2:9875000-9879200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr2:9875000-9879400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr2:9875000-9879400	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr2:9875200-9876800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr2:9875200-9877400	Enhancers	HMEC	breast
13	chr2:9875200-9877600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr2:9875200-9877600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr2:9875200-9877800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr2:9875200-9878800	Weak transcription	Colon Smooth Muscle	Colon
17	chr2:9875200-9879000	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr2:9875200-9879000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr2:9875200-9879000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr2:9875200-9879000	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr2:9875200-9879400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr2:9875200-9879400	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr2:9875400-9879000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr2:9875400-9879200	Enhancers	Primary T cells from cord blood	blood
25	chr2:9875600-9875800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr2:9875600-9875800	Enhancers	NHLF	lung
27	chr2:9875600-9877000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr2:9875600-9877400	Enhancers	Thymus	Thymus
29	chr2:9875800-9876000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:9875800-9876000	Enhancers	NHEK	skin
31	chr2:9875800-9877800	Enhancers	Fetal Thymus	thymus
32	chr2:9875800-9879200	Weak transcription	Esophagus	oesophagus
33	chr2:9876000-9876200	Enhancers	Duodenum Mucosa	Duodenum
34	chr2:9876000-9876400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr2:9876200-9878600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr2:9876400-9878800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:9876800-9878600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr2:9877000-9879000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:9877000-9879200	Enhancers	Fetal Muscle Leg	muscle
40	chr2:9877200-9877400	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr2:9877200-9877600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr2:9877200-9877600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr2:9877200-9877800	Enhancers	Fetal Muscle Trunk	muscle
44	chr2:9877400-9878000	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr2:9877400-9878800	Weak transcription	Thymus	Thymus
46	chr2:9877400-9885000	Weak transcription	HMEC	breast
47	chr2:9877600-9878600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr2:9877600-9878800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:9877600-9879000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr2:9877800-9878200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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