Variant report

Variant	nsv459944
Chromosome Location	chr2:169798619-169893419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1292)
CpG islands
(count:244)
Chromatin interactive
region (count:74)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1292 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:169866842-169866920	K562	blood:	n/a	n/a
2	ARID3A	chr2:169868699-169869030	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:169832421-169833511	K562	blood:	n/a	n/a
4	ARID3A	chr2:169858877-169859202	K562	blood:	n/a	n/a
5	ARID3A	chr2:169872456-169872885	K562	blood:	n/a	n/a
6	ARID3A	chr2:169799701-169800161	K562	blood:	n/a	n/a
7	ARID3A	chr2:169856185-169856281	K562	blood:	n/a	n/a
8	ARID3A	chr2:169818204-169818518	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:169802731-169802736	K562	blood:	n/a	n/a
10	ARID3A	chr2:169853529-169853808	K562	blood:	n/a	n/a
11	ARID3A	chr2:169808456-169808666	K562	blood:	n/a	n/a
12	ARID3A	chr2:169831095-169831177	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:169854959-169855697	K562	blood:	n/a	n/a
14	ARID3A	chr2:169868604-169869070	K562	blood:	n/a	n/a
15	ARID3A	chr2:169805127-169805433	K562	blood:	n/a	n/a
16	ATF1	chr2:169868575-169869069	K562	blood:	n/a	n/a
17	ATF1	chr2:169858936-169859135	K562	blood:	n/a	n/a
18	ATF1	chr2:169890772-169891106	K562	blood:	n/a	n/a
19	ATF1	chr2:169832562-169833108	K562	blood:	n/a	n/a
20	ATF1	chr2:169826069-169826169	K562	blood:	n/a	n/a
21	ATF1	chr2:169818178-169818487	K562	blood:	n/a	n/a
22	ATF1	chr2:169872537-169872814	K562	blood:	n/a	n/a
23	ATF3	chr2:169868668-169868978	K562	blood:	n/a	n/a
24	ATF3	chr2:169868652-169869113	K562	blood:	n/a	n/a
25	ATF3	chr2:169832565-169833091	K562	blood:	n/a	n/a
26	BACH1	chr2:169856269-169856475	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr2:169853751-169853883	K562	blood:	n/a	n/a
28	BACH1	chr2:169823592-169823640	K562	blood:	n/a	n/a
29	BACH1	chr2:169887855-169888196	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr2:169856153-169856545	K562	blood:	n/a	n/a
31	BACH1	chr2:169868647-169868982	K562	blood:	n/a	n/a
32	BACH1	chr2:169888050-169888066	K562	blood:	n/a	n/a
33	BCLAF1	chr2:169868559-169869172	K562	blood:	n/a	n/a
34	BCLAF1	chr2:169868545-169869209	K562	blood:	n/a	n/a
35	BHLHE40	chr2:169868716-169868992	HepG2	liver:	n/a	n/a
36	BHLHE40	chr2:169890820-169891165	K562	blood:	n/a	n/a
37	BHLHE40	chr2:169868593-169869161	K562	blood:	n/a	n/a
38	BHLHE40	chr2:169866501-169866826	GM12878	blood:	n/a	n/a
39	BHLHE40	chr2:169853601-169853961	K562	blood:	n/a	n/a
40	BHLHE40	chr2:169872498-169872845	K562	blood:	n/a	n/a
41	BHLHE40	chr2:169832407-169833178	K562	blood:	n/a	chr2:169832564-169832585
42	CBX3	chr2:169832416-169833369	K562	blood:	n/a	n/a
43	CBX3	chr2:169868556-169869119	HCT-116	colon:	n/a	n/a
44	CBX3	chr2:169890722-169891513	K562	blood:	n/a	n/a
45	CBX3	chr2:169808382-169808695	K562	blood:	n/a	n/a
46	CBX3	chr2:169868639-169869044	K562	blood:	n/a	n/a
47	CBX3	chr2:169817990-169818635	HCT-116	colon:	n/a	n/a
48	CBX3	chr2:169833817-169834617	K562	blood:	n/a	n/a
49	CBX3	chr2:169868561-169869244	HCT-116	colon:	n/a	n/a
50	CBX3	chr2:169891531-169892047	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:169888373-169888423	HL-60	blood:	n/a
2	chr2:169887819-169887869	HCT-116	colon:	n/a
3	chr2:169887819-169887869	MCF10A-Er-Src	breast:	n/a
4	chr2:169887275-169887325	AoSMC	blood vessel:	n/a
5	chr2:169887932-169887982	NT2-D1	testis:	n/a
6	chr2:169887932-169887982	HUVEC	blood vessel:	n/a
7	chr2:169887819-169887869	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:169887932-169887982	NHBE	bronchial:	n/a
9	chr2:169887819-169887869	BJ	skin:	n/a
10	chr2:169888373-169888423	HIPEpiC	eye:	n/a
11	chr2:169887819-169887869	GM12878	blood:	n/a
12	chr2:169888373-169888423	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:169887932-169887982	HepG2	liver:	n/a
14	chr2:169887275-169887325	SK-N-SH_RA	brain:	n/a
15	chr2:169887819-169887869	HRE	kidney:	n/a
16	chr2:169887819-169887869	SK-N-MC	brain:	n/a
17	chr2:169888373-169888423	HCPEpiC	choroid plexus:	n/a
18	chr2:169887932-169887982	PrEC	prostate:	n/a
19	chr2:169887275-169887325	HCF	heart:	n/a
20	chr2:169887819-169887869	PrEC	prostate:	n/a
21	chr2:169888373-169888423	Hela-S3	cervix:	n/a
22	chr2:169887275-169887325	H1-hESC	embryonic stem cell:	embryo
23	chr2:169887819-169887869	HRPEpiC	eye:	n/a
24	chr2:169887819-169887869	SK-N-SH_RA	brain:	n/a
25	chr2:169887932-169887982	A549	lung:	n/a
26	chr2:169887275-169887325	BJ	skin:	n/a
27	chr2:169888373-169888423	PrEC	prostate:	n/a
28	chr2:169888373-169888423	SAEC	small airway:	n/a
29	chr2:169887819-169887869	RPTEC	kidney:	n/a
30	chr2:169887819-169887869	GM12891	blood:	n/a
31	chr2:169888373-169888423	K562	blood:	n/a
32	chr2:169887275-169887325	Caco-2	colon:	n/a
33	chr2:169887275-169887325	HL-60	blood:	n/a
34	chr2:169887275-169887325	RPTEC	kidney:	n/a
35	chr2:169887819-169887869	K562	blood:	n/a
36	chr2:169887819-169887869	SKMC	muscle:	n/a
37	chr2:169887275-169887325	BE2_C	brain:	n/a
38	chr2:169887932-169887982	AG04449	skin:	fetal
39	chr2:169887932-169887982	SK-N-SH	brain:	n/a
40	chr2:169888373-169888423	BE2_C	brain:	n/a
41	chr2:169887932-169887982	HRE	kidney:	n/a
42	chr2:169887275-169887325	HRPEpiC	eye:	n/a
43	chr2:169887275-169887325	ProgFib	skin:	n/a
44	chr2:169887275-169887325	NHDF-neo	bronchial:	n/a
45	chr2:169887275-169887325	HRE	kidney:	n/a
46	chr2:169888373-169888423	HCT-116	colon:	n/a
47	chr2:169887819-169887869	AoSMC	blood vessel:	n/a
48	chr2:169887275-169887325	HEEpiC	esophagus:	n/a
49	chr2:169888373-169888423	GM12891	blood:	n/a
50	chr2:169887932-169887982	AG09309	skin:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:169834987..169837279-chr2:169894436..169897221,2	K562	blood:
2	chr2:169818061..169818745-chr2:170078037..170078977,2	MCF-7	breast:
3	chr2:169855719..169857704-chr2:169862059..169864554,2	K562	blood:
4	chr2:169792537..169795729-chr2:169800668..169803473,3	K562	blood:
5	chr2:169837951..169840445-chr2:169852795..169855730,2	K562	blood:
6	chr2:169630102..169630887-chr2:169804877..169805660,3	MCF-7	breast:
7	chr2:169817898..169818621-chr2:169988130..169988983,4	MCF-7	breast:
8	chr2:169888510..169892069-chr2:169892414..169896004,4	K562	blood:
9	chr2:169823383..169825754-chr2:169828486..169831450,3	K562	blood:
10	chr2:169852777..169855000-chr2:169871972..169874086,2	K562	blood:
11	chr2:169883024..169885522-chr2:169886192..169887692,2	K562	blood:
12	chr2:169817359..169819675-chr2:169839586..169842251,2	K562	blood:
13	chr2:169836644..169838508-chr2:169857437..169860261,2	K562	blood:
14	chr2:169887824..169890043-chr2:169893215..169894937,2	K562	blood:
15	chr2:169854536..169858017-chr2:169861100..169865668,5	K562	blood:
16	chr2:169881738..169885413-chr2:169888172..169891590,5	MCF-7	breast:
17	chr2:169833047..169834023-chr2:169868302..169869260,2	K562	blood:
18	chr2:169818313..169818917-chr2:170078254..170079024,2	MCF-7	breast:
19	chr2:169814051..169816137-chr2:169816733..169819588,2	MCF-7	breast:
20	chr2:169832771..169834585-chr2:169841588..169843585,2	K562	blood:
21	chr2:169835840..169838628-chr2:169849350..169851934,2	K562	blood:
22	chr2:169837951..169840445-chr2:169852795..169855730,2	K562	blood:
23	chr2:169881738..169885413-chr2:169888172..169891590,5	MCF-7	breast:
24	chr2:169817874..169818883-chr2:169988110..169989002,6	MCF-7	breast:
25	chr2:169848331..169850126-chr2:169852095..169853708,2	K562	blood:
26	chr2:169870894..169873075-chr2:169873508..169875798,2	MCF-7	breast:
27	chr2:169890402..169894081-chr2:169906491..169908836,3	K562	blood:
28	chr2:169822897..169824505-chr2:169824864..169827260,2	MCF-7	breast:
29	chr2:169872905..169875234-chr2:169879475..169881366,2	K562	blood:
30	chr2:169817853..169818805-chr2:169987476..169989129,6	K562	blood:
31	chr2:169888510..169892069-chr2:169892414..169896004,4	K562	blood:
32	chr2:169848331..169850126-chr2:169852095..169853708,2	K562	blood:
33	chr2:169816630..169819073-chr2:169825664..169828011,2	K562	blood:
34	chr2:169817863..169818829-chr2:169997380..169999266,9	K562	blood:
35	chr2:169884116..169886813-chr2:169918668..169921279,2	K562	blood:
36	chr2:169833047..169834023-chr2:169868302..169869260,2	K562	blood:
37	chr2:169824857..169827462-chr2:169828065..169830126,2	MCF-7	breast:
38	chr2:169855719..169857704-chr2:169862059..169864554,2	K562	blood:
39	chr2:169882226..169886162-chr2:169888719..169892906,7	K562	blood:
40	chr2:169837104..169839810-chr2:169841582..169843112,3	K562	blood:
41	chr2:169882130..169884017-chr2:169890019..169892429,2	K562	blood:
42	chr2:169869258..169873689-chr2:169882752..169886286,4	K562	blood:
43	chr2:169850086..169852097-chr2:169867701..169869340,2	K562	blood:
44	chr2:169817359..169819675-chr2:169839586..169842251,2	K562	blood:
45	chr2:169817863..169818742-chr2:170078413..170079041,3	K562	blood:
46	chr2:169804921..169805756-chr2:170253961..170254734,2	MCF-7	breast:
47	chr2:169792449..169795110-chr2:169797440..169799933,3	K562	blood:
48	chr2:169860709..169866766-chr2:169867937..169873832,7	K562	blood:
49	chr2:169837104..169839810-chr2:169841582..169843112,3	K562	blood:
50	chr2:169883024..169885522-chr2:169886192..169887692,2	K562	blood:

No data

Variant related genes	Relation type
ABCB11	TF binding region
ABCB11	CpG island
ENSG00000073734	chromatin interactions
ENSG00000138399	chromatin interactions

Extended variants
information (count: 3726 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:3726 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2685814	chr2:169798619-169798620	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552433423	chr2:169798636-169798637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566002137	chr2:169798637-169798638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535339554	chr2:169798652-169798653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138421062	chr2:169798703-169798704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35384412	chr2:169798713-169798714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568443297	chr2:169798724-169798725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs3084063	chr2:169798732-169798733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200248646	chr2:169798735-169798736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71003065	chr2:169798736-169798737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2216503	chr2:169798737-169798738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78505070	chr2:169798739-169798740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187090528	chr2:169798743-169798744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373975082	chr2:169798789-169798790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537145726	chr2:169798808-169798809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557530621	chr2:169798815-169798816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13407637	chr2:169798850-169798851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571530409	chr2:169798885-169798886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577095623	chr2:169798923-169798924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534153214	chr2:169798970-169798971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539671967	chr2:169798975-169798976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6709087	chr2:169799010-169799011	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs573014479	chr2:169799012-169799013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200105841	chr2:169799018-169799019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3067961	chr2:169799028-169799029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542111038	chr2:169799047-169799048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189614608	chr2:169799098-169799099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535678059	chr2:169799168-169799169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575238728	chr2:169799217-169799218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377103865	chr2:169799246-169799247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2250677	chr2:169799288-169799289	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs532887659	chr2:169799361-169799362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545951828	chr2:169799400-169799401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556285001	chr2:169799426-169799427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569416878	chr2:169799469-169799470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559904354	chr2:169799553-169799554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528729310	chr2:169799554-169799555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548145182	chr2:169799584-169799585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192998931	chr2:169799592-169799593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184758568	chr2:169799637-169799638	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143023203	chr2:169799773-169799774	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78393306	chr2:169799806-169799807	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570928706	chr2:169799822-169799823	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539950927	chr2:169799864-169799865	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189559615	chr2:169799885-169799886	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146159319	chr2:169799898-169799899	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558086286	chr2:169799899-169799900	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555671012	chr2:169799903-169799904	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377010878	chr2:169799986-169799987	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564243605	chr2:169800024-169800025	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

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	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
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
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Developmental delay	21147756	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
Breast cancer	22522925	CNVD
Sudden cardiac death	19188705	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169788200-169802600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:169793600-169799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:169796000-169801000	Strong transcription	Liver	Liver
4	chr2:169798400-169800000	Weak transcription	K562	blood
5	chr2:169798600-169799600	Weak transcription	Fetal Heart	heart
6	chr2:169799600-169800200	Enhancers	Fetal Heart	heart
7	chr2:169799800-169801200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:169800000-169801200	Enhancers	K562	blood
9	chr2:169801000-169802000	Genic enhancers	Liver	Liver
10	chr2:169802000-169802600	Weak transcription	Liver	Liver
11	chr2:169802600-169803600	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr2:169802600-169818000	Strong transcription	Liver	Liver
13	chr2:169804200-169804800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:169804200-169805200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:169804600-169805000	Enhancers	HMEC	breast
16	chr2:169804600-169805200	Active TSS	Aorta	Aorta
17	chr2:169808400-169812200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:169815200-169815600	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr2:169815600-169817400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr2:169816000-169816200	Enhancers	Brain Substantia Nigra	brain
21	chr2:169816000-169816400	Enhancers	Brain Angular Gyrus	brain
22	chr2:169816200-169816400	Flanking Active TSS	Brain Substantia Nigra	brain
23	chr2:169816400-169816600	Enhancers	Brain Substantia Nigra	brain
24	chr2:169816400-169816800	Enhancers	Brain Hippocampus Middle	brain
25	chr2:169816600-169816800	Flanking Active TSS	Brain Substantia Nigra	brain
26	chr2:169816800-169817000	Enhancers	Brain Substantia Nigra	brain
27	chr2:169817400-169819200	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr2:169818000-169818200	Enhancers	Brain Angular Gyrus	brain
29	chr2:169818000-169818600	Weak transcription	Liver	Liver
30	chr2:169818000-169818800	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr2:169818000-169819400	Enhancers	HUVEC	blood vessel
32	chr2:169818200-169818600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr2:169818200-169818600	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr2:169818200-169818800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr2:169818400-169818600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr2:169818600-169819200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr2:169818600-169819200	Enhancers	Primary hematopoietic stem cells	blood
38	chr2:169818600-169819800	Enhancers	Liver	Liver
39	chr2:169818600-169820400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr2:169818600-169820600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr2:169818600-169820800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr2:169818800-169820400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr2:169818800-169826600	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr2:169819000-169819200	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr2:169819000-169819400	Enhancers	Osteobl	bone
46	chr2:169819000-169819600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr2:169819200-169820600	Weak transcription	Primary hematopoietic stem cells	blood
48	chr2:169819200-169824200	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr2:169819400-169820600	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr2:169819400-169822400	Weak transcription	HUVEC	blood vessel

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