EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-00049 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr1:2185950-2188530 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs260508chr12187085hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr1:2187603-2187614TTCTTATCTGT+6.14
Gata1MA0035.3chr1:2187603-2187614TTCTTATCTGT+6.62
NR3C1MA0113.3chr1:2186846-2186863TGGAACACTGTGTCCTG+6.06
NR3C1MA0113.3chr1:2186846-2186863TGGAACACTGTGTCCTG-6.14
NR3C2MA0727.1chr1:2186846-2186863TGGAACACTGTGTCCTG-6.28
NR3C2MA0727.1chr1:2186846-2186863TGGAACACTGTGTCCTG+6.35
ZNF263MA0528.1chr1:2187877-2187898TTCTTCTCTGCCCCCTCCCTC-6.04
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_03761chr1:2186951-2187914Brain_Angular_Gyrus
SE_03761chr1:2188272-2188982Brain_Angular_Gyrus
SE_05718chr1:2186119-2189208Brain_Cingulate_Gyrus
SE_07454chr1:2186119-2189367Brain_Hippocampus_Middle_150
SE_08491chr1:2185789-2189149Brain_Inferior_Temporal_Lobe
SE_08969chr1:2187324-2187728Brain_Mid_Frontal_Lobe
SE_11007chr1:2184548-2192323CD20
SE_12005chr1:2184665-2189009CD3
SE_15942chr1:2185651-2188669CD4_Naive_Primary_7pool
SE_16427chr1:2185351-2189136CD4_Naive_Primary_8pool
SE_17042chr1:2184540-2189098CD4p_CD225int_CD127p_Tmem
SE_17322chr1:2181525-2189193CD4p_CD25-_CD45RAp_Naive
SE_17845chr1:2181649-2192081CD4p_CD25-_CD45ROp_Memory
SE_18345chr1:2184333-2191921CD4p_CD25-_Il17-_PMAstim_Th
SE_19191chr1:2185876-2189148CD4p_CD25-_Il17p_PMAstim_Th17
SE_20071chr1:2184982-2189278CD56
SE_21247chr1:2185434-2188617CD8_Memory_7pool
SE_21558chr1:2185341-2189061CD8_Naive_7pool
SE_21979chr1:2185169-2189317CD8_Naive_8pool
SE_22376chr1:2182855-2189180CD8_primiary
SE_41586chr1:2184798-2187019LNCaP
SE_41586chr1:2187683-2188254LNCaP
SE_46124chr1:2186130-2189227Osteoblasts
SE_62490chr1:2120386-2191742Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr121863192188200
Number: 1             
IDChromosomeStartEnd
GH01I002253chr121846312191030
Enhancer Sequence
CTTGATACTC AGTCTGGGTG CGTTGAAGAC GCGGCCTCTG GCTGTCAGCC TGTCCTTGTG 60
TGCAGTGACC GGTCTACCTG TCTGGCCTTG TGCCTAGACT TGTGGCCGTC ACCACTATCT 120
CTGGGGAGGG GTGAAGTGGA CTGGGAGGTA GGAGCCGAAT TGGAGTCTTC TCTTTGTTCC 180
TGAAGTTATC ACAGTCTTGG CCAGACTGTG GTCACTGCGT GCGTGTGTGT GTGTGTGTGA 240
TGCGCAGGGC ATTTGCTGGT GGAATAGCAC GGGCCATTGG CATTTGCACC TGAGGCGTGC 300
AGCCCCCCTG CTGCACACCT ATGGGGTCCC TGCGGTCAGG TGAGCTCTGG GGGGTTTCTG 360
AGGGTGGAGA CAGCCACAAC AACACTTCTT TCCTCCAAAT GCCTGTGCTG TGCACTTGGG 420
TGCAGGTGGC TTTTAGGGGA CATGGCTGGG CACTGCCCCA CAGTGTCACC TCTGTGTCCT 480
GTGGTGCGTG CTGTGGACTG GCACCACACC CCACGTGCTT GTTAGGCCAG TTTCTCTCAG 540
GTGTCGGTCA CCCTACCATG CGGCCTTTCT TTTGTCTTTT ATCTTTAGCT AAGGAGTCCA 600
TGGCATACCA AAAGCTGAAT GATGACAGCC AGTGTCCCCA TCCTGTCCTC CCCAACTTTC 660
CACAGGCAGG GACGCTCCCC ATTCTTGCTG CATAGTCTTC TGTTGACCCC ATGTACCTGA 720
GTGACCCCCA CGTACCTGAG TGTGACAAGC ACTATGGTGC TTGACCTCAG TCCAGCTGCT 780
TAGACCTGTA CCTGCCACAG CCCCACGTGC TGACACCTTG CGTCTTGAGT TTTGATAAAT 840
CTATCCTTTG GCTGATTAAT ATGACTGAGT GGTGTCTTCT GACCCCATTT CTTATCTGGA 900
ACACTGTGTC CTGACTTCAT TTCCTGTCTG GAGCACACTG TCCTGACCTC ATTTCCTGTC 960
TGGAACACAC TGTGTCCTGA CCTCATTTCC TGCCTGGAGC TCTCTGTGTC CTGACCTCAT 1020
TTCCTGTCTG TGCCGCTCTG TCCTGACCTC ATTTTCTGTC TGTGCCACCC TTTGTCCTGA 1080
CCTCATTTCC TGTCTGGAAC ATGCTGTGTC CTAACTGCAT TTCCTGTCTG GAGCTCTCTC 1140
TGTCCTGACC TCATTTCCTG TCTGGATCTC TCTATGTCCT GACCTCATTT CCTGTCTGGA 1200
ACATGCTGTA TCCTGATATC ATTTCCTGTC TGTGCCACTT TGTCCGGACC TCATTTTCTG 1260
TCTGGAGCAC TCTGTATCCT GACCTCATTT CCTGTTTGTG CCACCCTTTG TCCTGACCTC 1320
ATTTCCTGTC TGGAACATGC TGTGTCCGGA TTGCATTTCC TCTCTGGAGC TCTCTCTGTC 1380
CTGACCTCAT TTCCTGTCTG GAGCCAGTGA CCTCATTTCC TGTCTGTGTC ACTCTGTCCT 1440
GACCTCATTT CCTGTCTGTG CCACTCTTTG TCCTGACCTC ATTTCCTGTA TGCAACACAC 1500
TGTGCCCGGA CTGCATTTCC TGTCTGGAGC TCTCTCTGTC CTGATCTCAT TTCCTGTCAG 1560
GAGCACTCTG TGTACTGACC TCATTTCCTG TCTGTGCCAC TCTTGTGTCC TGACCTCTTT 1620
TCCAGTCTGT GCCACTCTGT GTCCTGACCT CATTTCTTAT CTGTGCCACT CTGTGTCCTG 1680
ACCTCATTTC CTGTCTGGAG CACTCTGTCC TGACCTCATT TCCTGTCTTG TGTCCTGACC 1740
TCATTTCCTG TCTGGAGCTC TCTGTGTCCT TACCTCATTT CCTGTCTGTG CTGCTTTCTG 1800
TCTTGGAGTT GCGTGCCTGA CCTCATTTCC TCTCCACTGT GTGTTCCTGG AGTTAGGCAT 1860
CATCTTGGTT TTTACTCCCT TGCTTGGTTT TCTCAGGATC TCTGGCTGCT CCGTCCTTGC 1920
TCCAGCGTTC TTCTCTGCCC CCTCCCTCTG TGGTCCAGAG GCCGATGGCC AGCTGGCCCT 1980
CACCTGCCCG CCCTGGGTAT TTCTGTGCTC TTCCTGGTGA GGGATTCTAG GGGTTCCCCT 2040
CCTGGGTTCA TCCTTACCTG AGTAGCCACA GCACACTGTG CAGTTGGGTG CCTGGGAGGC 2100
ACGTGCTTTG GGTGTTGCAT GGCTGACCTG GTAACTGGGC ACCCGTGTAT GGAGGGCTGG 2160
AACAGAACAC TTGTCGGCGC TCCTCAGCGT CTTGCCTCTG GTGTCCCCAT GGCGAAGTCC 2220
CCTGCCATCT GCTTTGGGCT CTGACATGTG ACCTGACTGT GCCCTTCAGG AGCTTTCAGA 2280
ACCTCCTCTT AGATCTGGCA TTCAAAATGT CTTGTCAGAC ACCTCGAGGC GGCTTGTGTT 2340
TGGCCCTGTG TTGGGCGCCT ATTGGGCCCT TGTCAGGTTT TTGTTGCCAG GAGGCTCGCG 2400
CCCCGATCTT CGGGATGGTG CCCGTGGCAT CTTCTGCTCG GTGCTCCCTA GGGCTGGACG 2460
TTGGTCCTCC TGGCACTGGT GCTCCGGTTG CTGTGGTCTC CCTGCTGTTC CCTTGTGGCT 2520
CAGGATTACT CTCTGGAGGT CTCCGCCTTA TCATGAGCAC TTTCTTTGTT GGCTACTTTT 2580