EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-08482 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr14:91868720-91871160 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs117297873chr1491870330hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr14:91870615-91870636ATCCTCTCCTTCCCCTCCTCC-6.97
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_03973chr14:91868501-91869636Brain_Anterior_Caudate
SE_09196chr14:91868323-91871210CD14
SE_10890chr14:91853239-91874080CD20
SE_11838chr14:91867869-91874199CD3
SE_14423chr14:91867825-91878373CD4_Memory_Primary_7pool
SE_15581chr14:91868198-91873746CD4_Memory_Primary_8pool
SE_16257chr14:91868680-91869818CD4_Naive_Primary_7pool
SE_16329chr14:91867866-91878413CD4_Naive_Primary_8pool
SE_16861chr14:91868494-91870042CD4p_CD225int_CD127p_Tmem
SE_16861chr14:91870119-91871173CD4p_CD225int_CD127p_Tmem
SE_17338chr14:91867815-91886176CD4p_CD25-_CD45RAp_Naive
SE_17763chr14:91852838-91886281CD4p_CD25-_CD45ROp_Memory
SE_18257chr14:91867732-91886272CD4p_CD25-_Il17-_PMAstim_Th
SE_19104chr14:91867817-91874225CD4p_CD25-_Il17p_PMAstim_Th17
SE_19998chr14:91867824-91884134CD56
SE_21071chr14:91867635-91878274CD8_Memory_7pool
SE_21656chr14:91868189-91874026CD8_Naive_7pool
SE_21949chr14:91867747-91878386CD8_Naive_8pool
SE_22293chr14:91852641-91884153CD8_primiary
SE_31363chr14:91868619-91870129Fetal_Thymus
SE_31609chr14:91867949-91871118Gastric
SE_39415chr14:91868917-91870072Jurkat
SE_39415chr14:91870172-91871126Jurkat
SE_41633chr14:91868601-91869042LNCaP
SE_41633chr14:91869178-91870093LNCaP
SE_41633chr14:91870127-91870808LNCaP
SE_43558chr14:91868926-91869931MM1S
SE_50173chr14:91867864-91871145Sigmoid_Colon
SE_52486chr14:91867931-91870114Small_Intestine
SE_52486chr14:91870152-91871020Small_Intestine
SE_53934chr14:91868949-91869857Spleen
SE_58376chr14:91781648-91886211Ly1
SE_58849chr14:91813006-91886123Ly3
SE_60717chr14:91860252-91886040DHL6
SE_61123chr14:91814842-91881922HBL1
SE_62324chr14:91813043-91886085Tonsil
SE_66290chr14:91868917-91870072Jurkat
SE_66290chr14:91870172-91871126Jurkat
SE_67160chr14:91868926-91869931MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr149187069691870882
chr149186932291869469
Enhancer Sequence
AGAGCATGCT TATCTAATAC AACTACCACA GAGGCTGACA TCTCAGAAAC AAGGCTGAGC 60
AGAGGAAGAA GTTACAGGCA GTGTGCTGCC GTTTATGGAA GTCTCGAAGA AAGATCACAC 120
AAAGCTGTGT GTGTGTGTAC ACAAGTGTGT ATAGTGTGCA CACACGCATA TATATACAAC 180
ACACACACAT AAACACAGCA AGCGGATAAA AGTGTTAAGT AGATACCACC CAATTAATGA 240
GAGGTGTTAA CCCCAGGAAG GGAGAGGACA ACAGGGCTTA GTAGTGGCTG CTGGGAACGT 300
CTATCTCAAG AGAAAATTTT TATTTCTTAA AAAAGGAAAA GGTCTCAAGC AAATATGGAA 360
AAATAGAACC GTATGTTCAT ATTTATTTTG AACGACAGGT ATGTGAGTGT TCGTTATGAC 420
CACTTGTACT GTTTTATTTT TAATTCTTCA AAACAATAAA GGAAAAAGAA AAGGGCTGGG 480
AGAAGCTAAG GCACCCGGGC TGTATTTATT CTGCTGTTTC ACTTGAGATA AGGAACCTTC 540
TGGCCTTGTG CCCATGCTAG AGGCCAGAAG TCAGAGAGCC GAGCTCAAGG AACCCAGAAA 600
GCTAAACTTC CTTGAGCTGA TCGTAAACTC TAAATCTCCT CTAAATCTCG CAGTTTCTGG 660
TCACCATGCA ACTGTAGCAT TTCAGGCCCA CCCCCTTTTG CTTGAAGGAG GGCACTCAGG 720
AGGCTCAGAG AAGGAGAGCA GCCCGCCCAG AGAGACGGCG GGACCCCAGC CTTGCTGCCT 780
CTGCACCTGG CGAGGAGAGG CGCATGAAGA AACAGCAAAT TCCTCATTTC AGAGTGAATC 840
CAATGGGTAA GTCCCCACAT CCATCCAAGG GTCCCGATCT CACTGGATGA GATATCCACG 900
TGTGGACTCG ATGACAAAGA CATACGTCTC CAACAACACA CAGGGAATGT ATCCAGGCCA 960
CCATCTGAAG TGCTTCCCGC CATACAAAGC CAAAGAAACC TCAGAAACTT CACATGACAA 1020
TGAGGCCCTT TCCAGACAAG GCGCCGGACT GAAGGTGTCC AGGGCAGGGA ATGGGGATGG 1080
GATGCCAGGC ACAACCCCAG AGCACAGACA GGCCAGCCAC TGCTGCACAG GGCGGACTTC 1140
TGCTGGAACA GCCTCACTTT CAGCCTGACT CCACTATCTG CATTTAATGT AAACATTCAA 1200
GGCTCTTAAT GAAAAAAGTG AACCATTACA TAAATCCAAA ATTTAATTTT AACAAAAGCC 1260
AGGCCAGACG CCGTGAGCCT TACAGGCTCG TGCCTATAAG CCCAGCACTT TGGGTGGCCA 1320
AGGCAGGAGG ACTGCTTGAG CTCCCAAGTT TGAGACCAGC CTGGCCAACA TAGTGAAACC 1380
CTGTCTCTAC TAAAAATACA AAAAGTAGCC AGGCGTGGTG GTGCCCACTG GTGGTCCCAG 1440
CTACTCGGGA GGCTGAGGTA GGAGGATCGC CTGAGCCCAG TGGAGGGGGA GGTTGCAGTG 1500
AGCTAAGACT ATACCACTGC ACTCTAGCCT GGGCGACAGA GAGAGACCCT ATCTCAAAAA 1560
ATTAAATTAA ATTTTTAAAA TGCCAGATGA AAAGGAGGTT GGCTGTTGAA TGAGTAAAAC 1620
AAGCATCGGA GGACACAGGG TAAACCTGGC CAGCCAGGCT GAGGCAGCGT GGGGCTCTGG 1680
CCCAGCCTTG CCTGTCCTCC AGGCTGCTCA GCAGATATCC CATTTGAGGG TGCTGTCCTA 1740
AAGCCGGTGT CCCCACATTG GACAGGCCAG CCTTTTCTTC TCCAAAATGC AGAGACTGAC 1800
CCAGGTGCTC TCTCTCCAAG GCTTTGTCCT ACTCTGGCTT TCTCTGCCCC TTCTCAGCTA 1860
CCCCCTCAAC ACCCCCTGCT CCCTCTGGTA ACCGCATCCT CTCCTTCCCC TCCTCCAGTC 1920
TGAGACCCTG CCTTCCTGTC CTGGGGCGGT GAGACGTGAA TCTGGTGTAT GTGATGGAGA 1980
AGGGTCACCT GGTGAGGACT GAGCTCCTTC TACCCAGGAG ATTCAGCTCA ACGTGACTCT 2040
TCTAGAAATC ACCAGAAATG TTCTAACCCA TTGGTTCCAG TGGTTCCCAT GGGCATGTGC 2100
GTCAGAATCA CCTGGGGGCC TGTTAAAATA CAGACTCCCA ACTTACATGC AGGCCCAACA 2160
ATCTGCATCT CTAACAAGCT CCCAGCGCGG CTGCAGATCT GGGGACCATC CTTTGAAGAA 2220
CCACCACTCT CACCCACTGA TTCTCAATCC TGTTGGAATG GTGAGACTCA AGAAGCTGGG 2280
AAATTTTTGA AAGTGCAGAT TCCTTGGCTG GGCGCGGTGG CTCACGCCTG TAATCCCAGC 2340
ACTTTGGGAG GCTGAGGCGG GTGGATCATG AAGTCAGGAG ATCGAGACCA TCCTGGCTAA 2400
CACGGTGAAA ACCCGTCTCT ACTAAAAATA CAAAAAAAAT 2440