EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS008-00093 
Organism
Homo sapiens 
Tissue/cell
BJ 
Coordinate
chr1:32419810-32421460 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:32420688-32420706GGCAGGCAGGGAGGAAGG+6.69
Nr2f6(var.2)MA0728.1chr1:32421324-32421339GAGGTCAAGAGTTCG+6.24
Number of super-enhancer constituents: 48             
IDCoordinateTissue/cell
SE_00185chr1:32419404-32424304Adipose_Nuclei
SE_01455chr1:32419850-32421402Adrenal_Gland
SE_03010chr1:32419859-32421333Bladder
SE_05505chr1:32420010-32421309Brain_Cingulate_Gyrus
SE_09496chr1:32418058-32428385CD14
SE_11611chr1:32420063-32422813CD20
SE_13610chr1:32419779-32422620CD34_Primary_RO01536
SE_14567chr1:32419441-32422703CD4_Memory_Primary_7pool
SE_18176chr1:32420050-32422535CD4p_CD25-_CD45ROp_Memory
SE_18474chr1:32419953-32422691CD4p_CD25-_Il17-_PMAstim_Th
SE_19618chr1:32420337-32421395CD4p_CD25-_Il17p_PMAstim_Th17
SE_20913chr1:32419675-32422740CD8_Memory_7pool
SE_24317chr1:32420064-32421233Colon_Crypt_2
SE_25246chr1:32420018-32421237Colon_Crypt_3
SE_25437chr1:32420012-32421504DND41
SE_26248chr1:32419683-32422741Duodenum_Smooth_Muscle
SE_27326chr1:32419664-32422845Esophagus
SE_28018chr1:32419790-32422410Fetal_Intestine
SE_29138chr1:32419770-32422630Fetal_Intestine_Large
SE_30289chr1:32419815-32421414Fetal_Muscle
SE_31027chr1:32419982-32421367Fetal_Thymus
SE_31788chr1:32419829-32421353Gastric
SE_32591chr1:32419775-32421553GM12878
SE_34572chr1:32419736-32421503HCT-116
SE_34675chr1:32416735-32424252HeLa
SE_37823chr1:32419700-32422879HSMMtube
SE_38810chr1:32419525-32422434HUVEC
SE_39284chr1:32419689-32421505IMR90
SE_39509chr1:32420170-32421199Jurkat
SE_39960chr1:32419682-32421505K562
SE_41137chr1:32418170-32422571Left_Ventricle
SE_42547chr1:32419802-32422957Lung
SE_45230chr1:32419766-32422360NHLF
SE_46136chr1:32419432-32422701Osteoblasts
SE_47391chr1:32419677-32422469Panc1
SE_47857chr1:32420067-32420906Pancreas
SE_47857chr1:32420913-32421256Pancreas
SE_49021chr1:32419814-32421380Right_Atrium
SE_50456chr1:32419774-32421378Sigmoid_Colon
SE_51637chr1:32419513-32422881Skeletal_Muscle
SE_52642chr1:32419822-32421514Small_Intestine
SE_53748chr1:32419851-32421396Spleen
SE_55181chr1:32420009-32421325Thymus
SE_56686chr1:32419684-32422618u87
SE_59623chr1:32331606-32430327Ly4
SE_62431chr1:32376082-32428121Tonsil
SE_64663chr1:32419773-32422373NHEK
SE_66311chr1:32420170-32421199Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr13242030732420572
Number: 1             
IDChromosomeStartEnd
GH01I031951chr13241714132426201
Enhancer Sequence
AGTAGAGACG GGATTTCACC ATGTTGGCCA GGCTGATCTC GAACTCCTGA CCTCAGGTGA 60
TCCACTCACC TCAACCTCCT AAAGTGCTGG GATTACAGGC ATGAGCCACC ACGCCTGGCC 120
CCTATGGTAG TTGCTTTTAA GTATAGAAAT GGAATTCCTG ATCGAGAGCC TCATAGTCAG 180
ATATTATTAT TGTTATTATT ATTTTTAAAA ATTTCTCTCT TTTTTTCTTT CCAGGCTGGT 240
GTCAAACTCC TGGCCTCAAG CCATCCTCCC ACCTCTGCCT CCCTAAGTGC TGGAATTACA 300
GATGTTAGCC ACTGTACCCG ACCTATTGTT AATAGTGTTA CATGTATAGA GAACCTGGCA 360
CTTAGTTGAC ACACCAAAAA CTTTACTTCC CAGCCTTTTC AGACCCTTTC CTCAGGCCAC 420
CCCACCTTTG CCTTCTCTTC AGCTTTCAAA TGTGTTGGCT ACTTCCCTTC CAGGCCAAGG 480
AGGTGCTGCT GGAGGTCTGT GTTCCTTCCA TAGCATCCCC CTTTTCCCCT CAGCCAAATG 540
AAGCGGAGAG GGCTTGGGCC TGACCCAGTG GCCTGCCCAC GTGGCTCCCC TGGAGACCGA 600
GGTAGGGGAA AAGGCAGAGA GTGCGTCAGT CCTGATGCAA TCACAGGCTT AGTGCTTGGC 660
TCACTTCCTC CTCTTTGGGT GTTTACGGGA GCCTGGATTC CACAGGAACC CTTGGAAGTG 720
TGCACTGACA ACAGAGTAGG GGGCAGACAG CATACAAAAT TATCCCTGCT TCAGGGACAG 780
TTCAGGAAGA AAGTGATACT GTGCCTGCCT GGGCCTCACA TGCCCTGAGC TCAGGGACAC 840
GGGAAAGAGA TACCAGGTGT CAAATCAGAG GCAGGGGAGG CAGGCAGGGA GGAAGGAGCC 900
AGGACAGGGG ACAAACCACT AGCTGCTGCC AGGGCCAGCT TCCAGACACA GCTCAGGGAG 960
GCTGTGAATA GGCCCTTTAT CTAAGCTGAA GTGGGGGAAA GGAATCACAG AAGGGGGTCT 1020
CAGGTGATAA GGAGCCTCAG AACAAGCTCA GGGGATCTTG TCCCTTCCTT CTCAGCAGAA 1080
ATCCTAGCAG GGGAGAAGCT TCTTTTTAAG GATTTTGTTT TCCAGCCATT TGCCCAGGAT 1140
CTTCATTTGG GAGGCCCCTC CTCAATCCCA CAGGCCTTAC TGGGTCACCT AGAGAGGTCC 1200
TAAGAGGTGC GGTGTTGCAC AGTGGTTAAG GACATGGGCT TTTGGCAGTC AAGTCTTAGC 1260
TCTTCCAGTG ACTGGCTGGA TACCCCAGGC AAGTCATTTC ACCTAACTCT CAACTCCCTA 1320
CGTCAAACAA GGATAATAAC AAGTAGTCAA CCCCAGAGAT AAAGCCGGGA GGCCCATAGA 1380
ACATTGCCTG GCAATGGTAA AAGCACTCAA TAACTGTTAG ATATTGTTAT TTTTATTAAG 1440
AATAAAGGAG CCGGGCATGG TGGCTCATGC CTGTAATCCC AGCACTTTGG GAGGCCGAGG 1500
TGGGCAGATC GCCTGAGGTC AAGAGTTCGA GACCAGCCTG ACCAACATGG AGAAACCCTG 1560
TCTCTACTAA AAATACAAAA TTAGCCAGGT ATGGTGGCAC ATGCCTGTAA TCCCAGCTAT 1620
TTAGGAGGCT GAGGCAGGAG AATCGCTTGA 1650