EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS053-18773 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr18:74782530-74784980 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr18:74782598-74782613TGACCTCTAACCCTT-6.18
STAT3MA0144.2chr18:74783862-74783873TTTCCCAGAAG-6.62
ZNF263MA0528.1chr18:74784111-74784132CCTCCCCTCCCCTCCTGCCTC-6.73
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_02301chr18:74782001-74785139Astrocytes
SE_09139chr18:74771371-74785241CD14
SE_11015chr18:74762704-74785115CD20
SE_12115chr18:74778461-74787202CD3
SE_13673chr18:74784180-74785205CD34_Primary_RO01536
SE_15038chr18:74778576-74784852CD4_Memory_Primary_7pool
SE_15651chr18:74778509-74786225CD4_Memory_Primary_8pool
SE_16468chr18:74778596-74785053CD4_Naive_Primary_8pool
SE_17255chr18:74778864-74784019CD4p_CD225int_CD127p_Tmem
SE_17959chr18:74771488-74787372CD4p_CD25-_CD45ROp_Memory
SE_18700chr18:74771421-74787762CD4p_CD25-_Il17-_PMAstim_Th
SE_19374chr18:74778282-74785130CD4p_CD25-_Il17p_PMAstim_Th17
SE_19981chr18:74771452-74788754CD56
SE_21261chr18:74778550-74784923CD8_Memory_7pool
SE_22307chr18:74770375-74789123CD8_primiary
SE_25341chr18:74771526-74785162DND41
SE_25885chr18:74783911-74785197Duodenum_Smooth_Muscle
SE_26884chr18:74782489-74784977Esophagus
SE_30168chr18:74783191-74784494Fetal_Muscle
SE_34994chr18:74773337-74785172HeLa
SE_39197chr18:74776594-74786600IMR90
SE_41189chr18:74783193-74785058Left_Ventricle
SE_42218chr18:74781323-74783055Lung
SE_42218chr18:74783324-74785105Lung
SE_44218chr18:74782828-74785072NHDF-Ad
SE_47137chr18:74774037-74784811Panc1
SE_49182chr18:74783332-74784361Right_Atrium
SE_51089chr18:74782985-74785181Skeletal_Muscle
SE_52417chr18:74782923-74785054Small_Intestine
SE_53332chr18:74771633-74785069Spleen
SE_58547chr18:74756065-74865317Ly1
SE_61817chr18:74764079-74793826Toledo
SE_62620chr18:74763866-74793718Tonsil
SE_65082chr18:74774799-74784762NHEK
SE_65574chr18:74782370-74783039Pancreatic_islets
SE_65574chr18:74784130-74784965Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr187478396474784198
Number: 1             
IDChromosomeStartEnd
GH18I077059chr187477155674787401
Enhancer Sequence
AAACCAGTGA TTAGTCTCAT TTTCTCTGTG TGTAAAAACA CAAAAACTAA AAACCCTCTA 60
CCCAGCCTTG ACCTCTAACC CTTAAGTGTC AAGCTTTCCC TGGGGGTCAG TGTGGCCCTG 120
CACGGGGCTC TGGGGCAGGT GACAGGAGGG GCCCTGGGAA CTCGAGAGGT CCACCCTCTC 180
CCGCCACTGA ATTGTGGAAG CGCAATTCAG TTTTCTTCAT CAGAACCGAG TGGAGAAGCA 240
AAGGATGGCA TGGAGTCAAA CTTCCCAAAG CCAGTCACAG CCAGGACGTC GGCGGGCGGA 300
ATCCTGGTTG GTTTTGAGGA CCCCGCTCAG GTGCTTGTTC CCGCGTAGCT GGAGTGTCCA 360
GCCAAGTGTG AGAGATCTCC TACCTGGTAC AGCTATTCAT GTACGTGCAC ACATGGCACA 420
CACGCACACG CACATTGTAG GTGAAAATAC GCTTATAATT AGCCTTACAT TTTTAAAAGA 480
TTGGTGGTCT GGAGGTGGCA ATTTCAGGAG GAATGGCCCA GAGGGTAAGT TTCTAATCAT 540
CACAAAAAAG GCTGTGAGAG AGGAAAACAC TTGCTTCGTA TTGGTACAAA CATTATACAG 600
CATATTCTTA AAGTCCTGAT TCAGACTAGA AACTGCTTAT CAGGAGAGGA AGGTGTTGAA 660
ACATGTTACA AAGTGACTCT CACCTGCAAA ACCAGTTGTA TGTTAGACTC GGAGTCATGG 720
TCCACCACAG GCTGCTGTAT TCAACACATG TAAGAGTTGA TTTTGAGAAT TTTTCAATCC 780
CTTAAAAAAT GCTGCATTTC CCTTAAAAAA TGCTGCATTA GGAGATGTCC TAAGCTTGTC 840
CAGCCCATCT TATTTTGTTG TTGCTCTTCT GTTTTGTTTT GTTTTAGGCT TTTAGCAACC 900
TGAAGCCATG GTTTTTAGTT TCTGTCTCTA GTGATAACCA GAACAGAAAG ATGAGGAAGG 960
GTCTTTACTG ACCCAACCAG GGACAGAAAC TAAGAATCCA TGACTGTATT CTCTCCTTGG 1020
ACACTTGAAG CCTTGAGTGG AGAATCACTG GCCTGGAAGC AGATAAAAGT CTTGTCTGGT 1080
TCTGCATCCT CAGTACCTTG CCACTCACCC ACTTGTTCCC ACCCATGCTT GCACCAAACC 1140
CTGCTCAGGA GCTGAGCATA CAAAGAAAAT AAGGTAGGAA GCCAAATTGG GTGCTTCAAA 1200
AATAAAGCTA GAGAAGCAAG CCCAGAATGT CAGATGGCGA CTGTCCAATT AAACTCGGTG 1260
AGCCAAGCCC TGTCCATCAC ACTGGAGAGT GTCAATGGCG TAGGAAGTGC ACCGTGTTTA 1320
TTTTTTCTGA GATTTCCCAG AAGAAAAATT ACAGTGATTC ATATTTCTAA AATTCCTAGG 1380
ATGTTTAACA AGAGAAGTTG CAACTGTCTT CCCCCTTCTG AATCTTATAC TCGACTGACC 1440
TTATTTAAAA AACAAAACAA ACAAAAAAGC CCAGCTGAAG CTTCCTATGA CGTCACAGGC 1500
GACACAGTCA TATGTGGCAC CTACATGCCA GCTGCTTGGC CTTTGAAGGC TCAGGATCCT 1560
GCCGGCGTAC ACACCCCTCC GCCTCCCCTC CCCTCCTGCC TCATAATTCT TATCTCATTT 1620
CTATGCACAA ATCTGAATAT GGCCTGGTGT TTCTCACAGC ACCACACATA TTTTGAGCCT 1680
TAGGTCATTT CAGAGGGGAT GCTACTAAAA GGCAGATATT TCTTTAAGTT TTCTTTACCT 1740
TCTGCCATAT TCCCTGCCGT AGACAGATCT AATTCACCCA GATATTTGCA GAAAATAGTT 1800
TGGGGGCATC AGGATCTGCA ACACATGTAC GTCGTATCAA AATCATTATT CGCATGACAG 1860
CCAAGACCTC GGGCTCTCTG AAGCTGATTG CCTGGGTAAC AGGGAAAATA ACTGAGTTTT 1920
CTGTACCTGT TTGCTCAGCT TTAAAATGAA CATTATAATC ATACTTTTCT ATGTGGTCAT 1980
CGTGAAGAGC ATTCAATAAG TGGAAACTGC TCTTTGCAGA AGCACACAAA ACTATTGAAA 2040
ATGCAGATCA GTAGCATCTT AGCTTCACAC TGTTATCAGA ATAAGCCCTT ATTTTTTCTC 2100
AGAACCATCA AAGCCACTTC TCAGGGGCTC TGGCCCAGGA CTCCTGGTGT GGCAGCAGAA 2160
ACAGTGGGAT GTAGTGCCGC CCGCAGCGCA GTTACTCAAA GTGAGATCTT AAGCGAGTCA 2220
AGCTCCCTCC ACCTCAGTAT CCCCAGGAGG ACAGTGGTCC CCATCTTGCG GCATCATTAT 2280
GAGGACTGCA AATGGCACAT TTCTCTGGAG GAAAGCTCAC TGCTTTTAGG ACGCCTGGCC 2340
TGTTCAGCCA TTGTCAGCAA TGGTCAACCC TCCTTGCTGG CAGCAACGTG TTCTTTCTGA 2400
ATCTTCGCCC ACTGCCATTG CCCTGTCTTA GATTCCTCTC CAATTAATCC 2450