Variant report

Variant	nsv1002568
Chromosome Location	chr2:111607532-111781442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1668)
CpG islands
(count:305)
Chromatin interactive
region (count:67)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1668 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:111765312-111765730	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:111619242-111619732	HepG2	liver:	n/a	n/a
3	ATF2	chr2:111615868-111616322	GM12878	blood:	n/a	n/a
4	ATF2	chr2:111622752-111623228	GM12878	blood:	n/a	n/a
5	ATF2	chr2:111629197-111629667	GM12878	blood:	n/a	n/a
6	ATF2	chr2:111622695-111623275	GM12878	blood:	n/a	n/a
7	ATF2	chr2:111615792-111616378	GM12878	blood:	n/a	n/a
8	ATF2	chr2:111632494-111633133	GM12878	blood:	n/a	n/a
9	ATF2	chr2:111639334-111639882	GM12878	blood:	n/a	n/a
10	BACH1	chr2:111663096-111663148	K562	blood:	n/a	n/a
11	BATF	chr2:111639556-111639889	GM12878	blood:	n/a	n/a
12	BATF	chr2:111639538-111639837	GM12878	blood:	n/a	n/a
13	BATF	chr2:111630458-111630777	GM12878	blood:	n/a	chr2:111630621-111630632
14	BATF	chr2:111622698-111623140	GM12878	blood:	n/a	chr2:111623063-111623073
15	BATF	chr2:111622737-111623123	GM12878	blood:	n/a	chr2:111623063-111623073
16	BATF	chr2:111624741-111624995	GM12878	blood:	n/a	n/a
17	BATF	chr2:111632580-111633070	GM12878	blood:	n/a	n/a
18	BATF	chr2:111629238-111629641	GM12878	blood:	n/a	n/a
19	BATF	chr2:111629186-111629619	GM12878	blood:	n/a	n/a
20	BATF	chr2:111630505-111630798	GM12878	blood:	n/a	chr2:111630621-111630632
21	BATF	chr2:111624673-111624965	GM12878	blood:	n/a	n/a
22	BATF	chr2:111632672-111633051	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:111639546-111639838	GM12878	blood:	n/a	n/a
24	BCL11A	chr2:111632869-111633155	GM12878	blood:	n/a	n/a
25	BCL11A	chr2:111629238-111629561	GM12878	blood:	n/a	n/a
26	BCL11A	chr2:111639539-111639880	GM12878	blood:	n/a	n/a
27	BCL3	chr2:111615868-111616250	GM12878	blood:	n/a	n/a
28	BCL3	chr2:111639525-111639825	GM12878	blood:	n/a	n/a
29	BCLAF1	chr2:111639381-111639882	GM12878	blood:	n/a	n/a
30	BCLAF1	chr2:111622708-111623111	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:111664225-111664476	K562	blood:	n/a	n/a
32	BHLHE40	chr2:111632538-111632915	K562	blood:	n/a	n/a
33	BHLHE40	chr2:111632500-111632817	HepG2	liver:	n/a	n/a
34	BHLHE40	chr2:111632495-111633138	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:111630488-111630908	GM12878	blood:	n/a	n/a
36	BHLHE40	chr2:111719343-111719501	GM12878	blood:	n/a	n/a
37	BHLHE40	chr2:111611143-111611428	GM12878	blood:	n/a	n/a
38	BHLHE40	chr2:111632092-111632288	GM12878	blood:	n/a	n/a
39	BHLHE40	chr2:111751470-111751890	K562	blood:	n/a	n/a
40	BHLHE40	chr2:111668087-111668350	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:111622697-111623181	GM12878	blood:	n/a	n/a
42	BHLHE40	chr2:111708551-111708872	K562	blood:	n/a	n/a
43	BHLHE40	chr2:111751463-111751840	HepG2	liver:	n/a	n/a
44	BHLHE40	chr2:111621396-111621608	GM12878	blood:	n/a	n/a
45	BHLHE40	chr2:111774070-111774233	K562	blood:	n/a	n/a
46	BHLHE40	chr2:111615873-111616287	GM12878	blood:	n/a	n/a
47	BHLHE40	chr2:111701203-111701216	HepG2	liver:	n/a	n/a
48	BHLHE40	chr2:111719244-111719411	K562	blood:	n/a	n/a
49	BHLHE40	chr2:111751478-111751851	GM12878	blood:	n/a	n/a
50	BHLHE40	chr2:111613162-111613337	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:111639212-111639262	AG09319	gingival:	n/a
2	chr2:111639212-111639262	HCM	heart:	n/a
3	chr2:111737646-111737696	AG04450	lung:	fetal
4	chr2:111623300-111623350	HCT-116	colon:	n/a
5	chr2:111633044-111633094	Hepatocyte	liver:	n/a
6	chr2:111623300-111623350	HCF	heart:	n/a
7	chr2:111623300-111623350	GM12892	blood:	n/a
8	chr2:111737646-111737696	PANC-1	pancreas:	n/a
9	chr2:111623300-111623350	H1-hESC	embryonic stem cell:	embryo
10	chr2:111662494-111662544	AG09319	gingival:	n/a
11	chr2:111662494-111662544	RPTEC	kidney:	n/a
12	chr2:111633044-111633094	HEEpiC	esophagus:	n/a
13	chr2:111639212-111639262	K562	blood:	n/a
14	chr2:111639212-111639262	HRPEpiC	eye:	n/a
15	chr2:111662494-111662544	U87	brain:	n/a
16	chr2:111633044-111633094	AG04449	skin:	fetal
17	chr2:111662494-111662544	PrEC	prostate:	n/a
18	chr2:111639212-111639262	HIPEpiC	eye:	n/a
19	chr2:111639212-111639262	HCT-116	colon:	n/a
20	chr2:111662494-111662544	GM19239	blood:	n/a
21	chr2:111633044-111633094	IMR90	lung:	fetal
22	chr2:111623300-111623350	HL-60	blood:	n/a
23	chr2:111662494-111662544	HCM	heart:	n/a
24	chr2:111633044-111633094	HUVEC	blood vessel:	n/a
25	chr2:111623300-111623350	GM12878	blood:	n/a
26	chr2:111737646-111737696	Jurkat	blood:	n/a
27	chr2:111639212-111639262	NH-A	brain:	n/a
28	chr2:111662494-111662544	AG10803	skin:	n/a
29	chr2:111737646-111737696	ovcar-3	ovarian:	n/a
30	chr2:111639212-111639262	HNPCEpiC	eye:	n/a
31	chr2:111737646-111737696	GM06990	blood:	n/a
32	chr2:111662494-111662544	SAEC	small airway:	n/a
33	chr2:111639212-111639262	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:111737646-111737696	AG09319	gingival:	n/a
35	chr2:111633044-111633094	A549	lung:	n/a
36	chr2:111623300-111623350	LNCaP	prostate:	n/a
37	chr2:111623300-111623350	Caco-2	colon:	n/a
38	chr2:111623300-111623350	SK-N-SH	brain:	n/a
39	chr2:111623300-111623350	AG09319	gingival:	n/a
40	chr2:111623300-111623350	GM06990	blood:	n/a
41	chr2:111737646-111737696	AG10803	skin:	n/a
42	chr2:111737646-111737696	CMK	blood:	n/a
43	chr2:111662494-111662544	HAEpiC	amniotic membrane:	n/a
44	chr2:111737646-111737696	HCM	heart:	n/a
45	chr2:111737646-111737696	PrEC	prostate:	n/a
46	chr2:111639212-111639262	MCF10A-Er-Src	breast:	n/a
47	chr2:111623300-111623350	PANC-1	pancreas:	n/a
48	chr2:111737646-111737696	HAEpiC	amniotic membrane:	n/a
49	chr2:111662494-111662544	Hela-S3	cervix:	n/a
50	chr2:111639212-111639262	AG10803	skin:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:111755985..111757580-chr2:111758045..111760842,2	MCF-7	breast:
2	chr2:111659330..111661560-chr2:111667127..111669037,2	K562	blood:
3	chr2:111645690..111647920-chr2:111650857..111653776,2	MCF-7	breast:
4	chr2:111755985..111757580-chr2:111758045..111760842,2	MCF-7	breast:
5	chr19:36066525..36067230-chr2:111654141..111654641,2	MCF-7	breast:
6	chr2:111611685..111612458-chr2:111874292..111875234,3	MCF-7	breast:
7	chr2:111606890..111608485-chr2:111612122..111613694,2	K562	blood:
8	chr2:111736021..111738383-chr2:111741871..111744743,2	K562	blood:
9	chr2:111695761..111698354-chr2:111863269..111865733,2	K562	blood:
10	chr2:111781251..111782971-chr2:111875963..111879619,3	MCF-7	breast:
11	chr2:111774043..111776327-chr2:111778491..111780974,2	K562	blood:
12	chr2:111766024..111768316-chr2:111771253..111772869,2	K562	blood:
13	chr2:111774043..111778118-chr2:111778491..111781647,4	K562	blood:
14	chr2:111595145..111597268-chr2:111609719..111611330,2	K562	blood:
15	chr2:111772841..111774627-chr2:111779212..111780860,2	MCF-7	breast:
16	chr2:111706009..111708285-chr2:111713250..111715688,2	MCF-7	breast:
17	chr2:111729518..111731846-chr2:111877680..111879315,2	MCF-7	breast:
18	chr2:111750836..111753179-chr2:111879308..111880841,2	MCF-7	breast:
19	chr2:111652533..111654321-chr2:111657541..111660386,2	K562	blood:
20	chr2:111623256..111625222-chr2:111876740..111879332,2	MCF-7	breast:
21	chr2:111613927..111616498-chr2:111625288..111627633,2	K562	blood:
22	chr2:111755868..111757843-chr2:111761863..111764487,2	MCF-7	breast:
23	chr2:111777915..111779966-chr2:111780701..111783354,2	MCF-7	breast:
24	chr2:111774043..111776327-chr2:111778491..111780974,2	K562	blood:
25	chr2:111626175..111629011-chr2:111629051..111632531,5	K562	blood:
26	chr2:111630021..111632661-chr2:111644852..111646520,2	K562	blood:
27	chr2:111732418..111734781-chr2:111735661..111737326,2	K562	blood:
28	chr2:111603779..111605764-chr2:111610713..111613145,2	K562	blood:
29	chr2:111569200..111569886-chr2:111611955..111612624,2	MCF-7	breast:
30	chr2:111777915..111779966-chr2:111780701..111783354,2	MCF-7	breast:
31	chr2:111589730..111592608-chr2:111607480..111611247,3	MCF-7	breast:
32	chr2:111736021..111738383-chr2:111741871..111744743,2	K562	blood:
33	chr2:111726104..111728832-chr2:111876784..111878487,2	K562	blood:
34	chr2:111626175..111629011-chr2:111629051..111632341,3	K562	blood:
35	chr2:111774043..111778118-chr2:111778491..111781647,4	K562	blood:
36	chr2:111659330..111661560-chr2:111667127..111669037,2	K562	blood:
37	chr2:111601975..111604042-chr2:111606034..111607594,2	MCF-7	breast:
38	chr2:111732418..111734781-chr2:111735661..111737326,2	K562	blood:
39	chr2:111645690..111647920-chr2:111650857..111653776,2	MCF-7	breast:
40	chr2:111772841..111774627-chr2:111779212..111780860,2	MCF-7	breast:
41	chr2:111755868..111757843-chr2:111761863..111764487,2	MCF-7	breast:
42	chr2:111626175..111629011-chr2:111629051..111632531,5	K562	blood:
43	chr2:111741788..111745598-chr2:111748398..111751516,4	MCF-7	breast:
44	chr2:111618005..111620750-chr2:111621836..111623864,4	MCF-7	breast:
45	chr2:111695965..111698914-chr2:111704650..111707242,2	MCF-7	breast:
46	chr2:111777002..111779950-chr2:111790531..111792084,2	MCF-7	breast:
47	chr2:111706009..111708285-chr2:111713250..111715688,2	MCF-7	breast:
48	chr2:111650917..111653257-chr2:111655210..111658130,2	K562	blood:
49	chr2:111604170..111606952-chr2:111619066..111621745,2	MCF-7	breast:
50	chr2:111618005..111620750-chr2:111621836..111623864,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCL2L11-4	chr2:111739331-111739511	NONHSAT073609
2	lnc-BCL2L11-4	chr2:111753493-111753928	NONHSAT073609
3	lnc-BCL2L11-4	chr2:111775464-111775650	NONHSAT073610
4	lnc-BCL2L11-4	chr2:111774089-111774306	NONHSAT073610
5	lnc-BCL2L11-4	chr2:111753534-111753581	NONHSAT073610

No data

Variant related genes	Relation type
ACOXL	TF binding region
RPL5P9	TF binding region
ACOXL	CpG island
RPL5P9	CpG island
ENSG00000153093	chromatin interactions
ENSG00000153094	chromatin interactions

Extended variants
information (count: 6427 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:6427 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561038034	chr2:111607567-111607568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs145296079	chr2:111607595-111607596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543780646	chr2:111607619-111607620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72832868	chr2:111607676-111607677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs200867442	chr2:111607698-111607699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549954254	chr2:111607727-111607728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6732565	chr2:111607832-111607833	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
8	rs189037659	chr2:111607879-111607880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552815670	chr2:111607900-111607901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147652809	chr2:111608016-111608017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192981857	chr2:111608033-111608034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547553213	chr2:111608056-111608057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74955714	chr2:111608079-111608080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76201494	chr2:111608089-111608090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112435262	chr2:111608102-111608103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569866111	chr2:111608106-111608107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6736351	chr2:111608107-111608108	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs143107606	chr2:111608166-111608167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs57195687	chr2:111608180-111608181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs13410480	chr2:111608186-111608187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558323072	chr2:111608191-111608192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554672449	chr2:111608207-111608208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574850513	chr2:111608208-111608209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576914446	chr2:111608273-111608274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543470598	chr2:111608294-111608295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563661550	chr2:111608335-111608336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140160794	chr2:111608336-111608337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79278407	chr2:111608337-111608338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560076344	chr2:111608373-111608374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528728491	chr2:111608383-111608384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75277896	chr2:111608390-111608391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374323354	chr2:111608391-111608392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560841739	chr2:111608400-111608401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs117557420	chr2:111608417-111608418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529759879	chr2:111608426-111608427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145383475	chr2:111608429-111608430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569681984	chr2:111608435-111608436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs137881334	chr2:111608515-111608516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142395697	chr2:111608526-111608527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7588925	chr2:111608534-111608535	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs534533854	chr2:111608537-111608538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560796310	chr2:111608550-111608551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554718062	chr2:111608574-111608575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574847478	chr2:111608670-111608671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9917288	chr2:111608722-111608723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557169870	chr2:111608768-111608769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373163820	chr2:111608774-111608775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188886965	chr2:111608779-111608780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546200798	chr2:111608925-111608926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377438796	chr2:111608947-111608948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1087 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111596400-111611600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:111596800-111609600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr2:111597000-111611400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr2:111600800-111607600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr2:111601400-111611000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr2:111601600-111609200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr2:111601800-111609400	Weak transcription	Spleen	Spleen
8	chr2:111601800-111611600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr2:111604000-111611600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr2:111604600-111609800	Weak transcription	Primary B cells from cord blood	blood
11	chr2:111604800-111615800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr2:111605000-111609000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:111605000-111609400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr2:111605000-111611600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:111605400-111609000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr2:111605400-111609400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:111605600-111608400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr2:111605600-111608800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr2:111605600-111610200	Weak transcription	Primary B cells from peripheral blood	blood
20	chr2:111605800-111608600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr2:111605800-111609000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr2:111605800-111609200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr2:111606000-111608800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr2:111606000-111609200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr2:111606200-111608600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr2:111606200-111608800	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr2:111606400-111608400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr2:111606600-111608200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr2:111606600-111608600	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr2:111606600-111609000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr2:111606800-111608400	Weak transcription	Fetal Thymus	thymus
32	chr2:111606800-111608400	Weak transcription	Dnd41	blood
33	chr2:111607000-111609000	Weak transcription	Primary T cells from cord blood	blood
34	chr2:111607600-111608000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr2:111608000-111618800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr2:111608200-111613000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr2:111608400-111609200	Enhancers	H1 Cell Line	embryonic stem cell
38	chr2:111608400-111610400	Enhancers	Dnd41	blood
39	chr2:111608400-111610800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr2:111608400-111611800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr2:111608400-111613400	Enhancers	Fetal Thymus	thymus
42	chr2:111608600-111612400	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr2:111608600-111612600	Enhancers	Primary T cells fromperipheralblood	blood
44	chr2:111608600-111612600	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr2:111608800-111611800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr2:111608800-111612000	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr2:111608800-111612000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr2:111609000-111609800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:111609000-111610000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:111609000-111611000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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