EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-00057 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr1:2185720-2188300 
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_05718chr1:2184573-2186113Brain_Cingulate_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
ATGCGTGGTG CCCGTTGGAG GGGGTGGGAG GGCTCGGCTC TGCTCTCCCC CCGTGGGTCT 60
TCGTGTCACA GGGTGCTTGG GGGACTCTGC TGCACTGAGA TCTCCAGCGT GACATGTCCC 120
CGTCCCAAAC AGCCCTGAAA TGGCAATGCC TCATCCTAGG ATTACCGTCC CTTCCCGAAG 180
GCTTGAGGTC CTACTTAGAT GTCTACTGGA CTGCTTTTTA TTTTAATTTA CTTGATACTC 240
AGTCTGGGTG CGTTGAAGAC GCGGCCTCTG GCTGTCAGCC TGTCCTTGTG TGCAGTGACC 300
GGTCTACCTG TCTGGCCTTG TGCCTAGACT TGTGGCCGTC ACCACTATCT CTGGGGAGGG 360
GTGAAGTGGA CTGGGAGGTA GGAGCCGAAT TGGAGTCTTC TCTTTGTTCC TGAAGTTATC 420
ACAGTCTTGG CCAGACTGTG GTCACTGCGT GCGTGTGTGT GTGTGTGTGA TGCGCAGGGC 480
ATTTGCTGGT GGAATAGCAC GGGCCATTGG CATTTGCACC TGAGGCGTGC AGCCCCCCTG 540
CTGCACACCT ATGGGGTCCC TGCGGTCAGG TGAGCTCTGG GGGGTTTCTG AGGGTGGAGA 600
CAGCCACAAC AACACTTCTT TCCTCCAAAT GCCTGTGCTG TGCACTTGGG TGCAGGTGGC 660
TTTTAGGGGA CATGGCTGGG CACTGCCCCA CAGTGTCACC TCTGTGTCCT GTGGTGCGTG 720
CTGTGGACTG GCACCACACC CCACGTGCTT GTTAGGCCAG TTTCTCTCAG GTGTCGGTCA 780
CCCTACCATG CGGCCTTTCT TTTGTCTTTT ATCTTTAGCT AAGGAGTCCA TGGCATACCA 840
AAAGCTGAAT GATGACAGCC AGTGTCCCCA TCCTGTCCTC CCCAACTTTC CACAGGCAGG 900
GACGCTCCCC ATTCTTGCTG CATAGTCTTC TGTTGACCCC ATGTACCTGA GTGACCCCCA 960
CGTACCTGAG TGTGACAAGC ACTATGGTGC TTGACCTCAG TCCAGCTGCT TAGACCTGTA 1020
CCTGCCACAG CCCCACGTGC TGACACCTTG CGTCTTGAGT TTTGATAAAT CTATCCTTTG 1080
GCTGATTAAT ATGACTGAGT GGTGTCTTCT GACCCCATTT CTTATCTGGA ACACTGTGTC 1140
CTGACTTCAT TTCCTGTCTG GAGCACACTG TCCTGACCTC ATTTCCTGTC TGGAACACAC 1200
TGTGTCCTGA CCTCATTTCC TGCCTGGAGC TCTCTGTGTC CTGACCTCAT TTCCTGTCTG 1260
TGCCGCTCTG TCCTGACCTC ATTTTCTGTC TGTGCCACCC TTTGTCCTGA CCTCATTTCC 1320
TGTCTGGAAC ATGCTGTGTC CTAACTGCAT TTCCTGTCTG GAGCTCTCTC TGTCCTGACC 1380
TCATTTCCTG TCTGGATCTC TCTATGTCCT GACCTCATTT CCTGTCTGGA ACATGCTGTA 1440
TCCTGATATC ATTTCCTGTC TGTGCCACTT TGTCCGGACC TCATTTTCTG TCTGGAGCAC 1500
TCTGTATCCT GACCTCATTT CCTGTTTGTG CCACCCTTTG TCCTGACCTC ATTTCCTGTC 1560
TGGAACATGC TGTGTCCGGA TTGCATTTCC TCTCTGGAGC TCTCTCTGTC CTGACCTCAT 1620
TTCCTGTCTG GAGCCAGTGA CCTCATTTCC TGTCTGTGTC ACTCTGTCCT GACCTCATTT 1680
CCTGTCTGTG CCACTCTTTG TCCTGACCTC ATTTCCTGTA TGCAACACAC TGTGCCCGGA 1740
CTGCATTTCC TGTCTGGAGC TCTCTCTGTC CTGATCTCAT TTCCTGTCAG GAGCACTCTG 1800
TGTACTGACC TCATTTCCTG TCTGTGCCAC TCTTGTGTCC TGACCTCTTT TCCAGTCTGT 1860
GCCACTCTGT GTCCTGACCT CATTTCTTAT CTGTGCCACT CTGTGTCCTG ACCTCATTTC 1920
CTGTCTGGAG CACTCTGTCC TGACCTCATT TCCTGTCTTG TGTCCTGACC TCATTTCCTG 1980
TCTGGAGCTC TCTGTGTCCT TACCTCATTT CCTGTCTGTG CTGCTTTCTG TCTTGGAGTT 2040
GCGTGCCTGA CCTCATTTCC TCTCCACTGT GTGTTCCTGG AGTTAGGCAT CATCTTGGTT 2100
TTTACTCCCT TGCTTGGTTT TCTCAGGATC TCTGGCTGCT CCGTCCTTGC TCCAGCGTTC 2160
TTCTCTGCCC CCTCCCTCTG TGGTCCAGAG GCCGATGGCC AGCTGGCCCT CACCTGCCCG 2220
CCCTGGGTAT TTCTGTGCTC TTCCTGGTGA GGGATTCTAG GGGTTCCCCT CCTGGGTTCA 2280
TCCTTACCTG AGTAGCCACA GCACACTGTG CAGTTGGGTG CCTGGGAGGC ACGTGCTTTG 2340
GGTGTTGCAT GGCTGACCTG GTAACTGGGC ACCCGTGTAT GGAGGGCTGG AACAGAACAC 2400
TTGTCGGCGC TCCTCAGCGT CTTGCCTCTG GTGTCCCCAT GGCGAAGTCC CCTGCCATCT 2460
GCTTTGGGCT CTGACATGTG ACCTGACTGT GCCCTTCAGG AGCTTTCAGA ACCTCCTCTT 2520
AGATCTGGCA TTCAAAATGT CTTGTCAGAC ACCTCGAGGC GGCTTGTGTT TGGCCCTGTG 2580