EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS041-00084 
Organism
Homo sapiens 
Tissue/cell
EWS502 
Coordinate
chr1:2186050-2188460 
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: 23             
IDCoordinateTissue/cell
SE_03761chr1:2186951-2187914Brain_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
TGTGGCCGTC ACCACTATCT CTGGGGAGGG GTGAAGTGGA CTGGGAGGTA GGAGCCGAAT 60
TGGAGTCTTC TCTTTGTTCC TGAAGTTATC ACAGTCTTGG CCAGACTGTG GTCACTGCGT 120
GCGTGTGTGT GTGTGTGTGA TGCGCAGGGC ATTTGCTGGT GGAATAGCAC GGGCCATTGG 180
CATTTGCACC TGAGGCGTGC AGCCCCCCTG CTGCACACCT ATGGGGTCCC TGCGGTCAGG 240
TGAGCTCTGG GGGGTTTCTG AGGGTGGAGA CAGCCACAAC AACACTTCTT TCCTCCAAAT 300
GCCTGTGCTG TGCACTTGGG TGCAGGTGGC TTTTAGGGGA CATGGCTGGG CACTGCCCCA 360
CAGTGTCACC TCTGTGTCCT GTGGTGCGTG CTGTGGACTG GCACCACACC CCACGTGCTT 420
GTTAGGCCAG TTTCTCTCAG GTGTCGGTCA CCCTACCATG CGGCCTTTCT TTTGTCTTTT 480
ATCTTTAGCT AAGGAGTCCA TGGCATACCA AAAGCTGAAT GATGACAGCC AGTGTCCCCA 540
TCCTGTCCTC CCCAACTTTC CACAGGCAGG GACGCTCCCC ATTCTTGCTG CATAGTCTTC 600
TGTTGACCCC ATGTACCTGA GTGACCCCCA CGTACCTGAG TGTGACAAGC ACTATGGTGC 660
TTGACCTCAG TCCAGCTGCT TAGACCTGTA CCTGCCACAG CCCCACGTGC TGACACCTTG 720
CGTCTTGAGT TTTGATAAAT CTATCCTTTG GCTGATTAAT ATGACTGAGT GGTGTCTTCT 780
GACCCCATTT CTTATCTGGA ACACTGTGTC CTGACTTCAT TTCCTGTCTG GAGCACACTG 840
TCCTGACCTC ATTTCCTGTC TGGAACACAC TGTGTCCTGA CCTCATTTCC TGCCTGGAGC 900
TCTCTGTGTC CTGACCTCAT TTCCTGTCTG TGCCGCTCTG TCCTGACCTC ATTTTCTGTC 960
TGTGCCACCC TTTGTCCTGA CCTCATTTCC TGTCTGGAAC ATGCTGTGTC CTAACTGCAT 1020
TTCCTGTCTG GAGCTCTCTC TGTCCTGACC TCATTTCCTG TCTGGATCTC TCTATGTCCT 1080
GACCTCATTT CCTGTCTGGA ACATGCTGTA TCCTGATATC ATTTCCTGTC TGTGCCACTT 1140
TGTCCGGACC TCATTTTCTG TCTGGAGCAC TCTGTATCCT GACCTCATTT CCTGTTTGTG 1200
CCACCCTTTG TCCTGACCTC ATTTCCTGTC TGGAACATGC TGTGTCCGGA TTGCATTTCC 1260
TCTCTGGAGC TCTCTCTGTC CTGACCTCAT TTCCTGTCTG GAGCCAGTGA CCTCATTTCC 1320
TGTCTGTGTC ACTCTGTCCT GACCTCATTT CCTGTCTGTG CCACTCTTTG TCCTGACCTC 1380
ATTTCCTGTA TGCAACACAC TGTGCCCGGA CTGCATTTCC TGTCTGGAGC TCTCTCTGTC 1440
CTGATCTCAT TTCCTGTCAG GAGCACTCTG TGTACTGACC TCATTTCCTG TCTGTGCCAC 1500
TCTTGTGTCC TGACCTCTTT TCCAGTCTGT GCCACTCTGT GTCCTGACCT CATTTCTTAT 1560
CTGTGCCACT CTGTGTCCTG ACCTCATTTC CTGTCTGGAG CACTCTGTCC TGACCTCATT 1620
TCCTGTCTTG TGTCCTGACC TCATTTCCTG TCTGGAGCTC TCTGTGTCCT TACCTCATTT 1680
CCTGTCTGTG CTGCTTTCTG TCTTGGAGTT GCGTGCCTGA CCTCATTTCC TCTCCACTGT 1740
GTGTTCCTGG AGTTAGGCAT CATCTTGGTT TTTACTCCCT TGCTTGGTTT TCTCAGGATC 1800
TCTGGCTGCT CCGTCCTTGC TCCAGCGTTC TTCTCTGCCC CCTCCCTCTG TGGTCCAGAG 1860
GCCGATGGCC AGCTGGCCCT CACCTGCCCG CCCTGGGTAT TTCTGTGCTC TTCCTGGTGA 1920
GGGATTCTAG GGGTTCCCCT CCTGGGTTCA TCCTTACCTG AGTAGCCACA GCACACTGTG 1980
CAGTTGGGTG CCTGGGAGGC ACGTGCTTTG GGTGTTGCAT GGCTGACCTG GTAACTGGGC 2040
ACCCGTGTAT GGAGGGCTGG AACAGAACAC TTGTCGGCGC TCCTCAGCGT CTTGCCTCTG 2100
GTGTCCCCAT GGCGAAGTCC CCTGCCATCT GCTTTGGGCT CTGACATGTG ACCTGACTGT 2160
GCCCTTCAGG AGCTTTCAGA ACCTCCTCTT AGATCTGGCA TTCAAAATGT CTTGTCAGAC 2220
ACCTCGAGGC GGCTTGTGTT TGGCCCTGTG TTGGGCGCCT ATTGGGCCCT TGTCAGGTTT 2280
TTGTTGCCAG GAGGCTCGCG CCCCGATCTT CGGGATGGTG CCCGTGGCAT CTTCTGCTCG 2340
GTGCTCCCTA GGGCTGGACG TTGGTCCTCC TGGCACTGGT GCTCCGGTTG CTGTGGTCTC 2400
CCTGCTGTTC 2410