EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS053-00050 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr1:2186060-2189100 
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
ACCACTATCT CTGGGGAGGG GTGAAGTGGA CTGGGAGGTA GGAGCCGAAT TGGAGTCTTC 60
TCTTTGTTCC TGAAGTTATC ACAGTCTTGG CCAGACTGTG GTCACTGCGT GCGTGTGTGT 120
GTGTGTGTGA TGCGCAGGGC ATTTGCTGGT GGAATAGCAC GGGCCATTGG CATTTGCACC 180
TGAGGCGTGC AGCCCCCCTG CTGCACACCT ATGGGGTCCC TGCGGTCAGG TGAGCTCTGG 240
GGGGTTTCTG AGGGTGGAGA CAGCCACAAC AACACTTCTT TCCTCCAAAT GCCTGTGCTG 300
TGCACTTGGG TGCAGGTGGC TTTTAGGGGA CATGGCTGGG CACTGCCCCA CAGTGTCACC 360
TCTGTGTCCT GTGGTGCGTG CTGTGGACTG GCACCACACC CCACGTGCTT GTTAGGCCAG 420
TTTCTCTCAG GTGTCGGTCA CCCTACCATG CGGCCTTTCT TTTGTCTTTT ATCTTTAGCT 480
AAGGAGTCCA TGGCATACCA AAAGCTGAAT GATGACAGCC AGTGTCCCCA TCCTGTCCTC 540
CCCAACTTTC CACAGGCAGG GACGCTCCCC ATTCTTGCTG CATAGTCTTC TGTTGACCCC 600
ATGTACCTGA GTGACCCCCA CGTACCTGAG TGTGACAAGC ACTATGGTGC TTGACCTCAG 660
TCCAGCTGCT TAGACCTGTA CCTGCCACAG CCCCACGTGC TGACACCTTG CGTCTTGAGT 720
TTTGATAAAT CTATCCTTTG GCTGATTAAT ATGACTGAGT GGTGTCTTCT GACCCCATTT 780
CTTATCTGGA ACACTGTGTC CTGACTTCAT TTCCTGTCTG GAGCACACTG TCCTGACCTC 840
ATTTCCTGTC TGGAACACAC TGTGTCCTGA CCTCATTTCC TGCCTGGAGC TCTCTGTGTC 900
CTGACCTCAT TTCCTGTCTG TGCCGCTCTG TCCTGACCTC ATTTTCTGTC TGTGCCACCC 960
TTTGTCCTGA CCTCATTTCC TGTCTGGAAC ATGCTGTGTC CTAACTGCAT TTCCTGTCTG 1020
GAGCTCTCTC TGTCCTGACC TCATTTCCTG TCTGGATCTC TCTATGTCCT GACCTCATTT 1080
CCTGTCTGGA ACATGCTGTA TCCTGATATC ATTTCCTGTC TGTGCCACTT TGTCCGGACC 1140
TCATTTTCTG TCTGGAGCAC TCTGTATCCT GACCTCATTT CCTGTTTGTG CCACCCTTTG 1200
TCCTGACCTC ATTTCCTGTC TGGAACATGC TGTGTCCGGA TTGCATTTCC TCTCTGGAGC 1260
TCTCTCTGTC CTGACCTCAT TTCCTGTCTG GAGCCAGTGA CCTCATTTCC TGTCTGTGTC 1320
ACTCTGTCCT GACCTCATTT CCTGTCTGTG CCACTCTTTG TCCTGACCTC ATTTCCTGTA 1380
TGCAACACAC TGTGCCCGGA CTGCATTTCC TGTCTGGAGC TCTCTCTGTC CTGATCTCAT 1440
TTCCTGTCAG GAGCACTCTG TGTACTGACC TCATTTCCTG TCTGTGCCAC TCTTGTGTCC 1500
TGACCTCTTT TCCAGTCTGT GCCACTCTGT GTCCTGACCT CATTTCTTAT CTGTGCCACT 1560
CTGTGTCCTG ACCTCATTTC CTGTCTGGAG CACTCTGTCC TGACCTCATT TCCTGTCTTG 1620
TGTCCTGACC TCATTTCCTG TCTGGAGCTC TCTGTGTCCT TACCTCATTT CCTGTCTGTG 1680
CTGCTTTCTG TCTTGGAGTT GCGTGCCTGA CCTCATTTCC TCTCCACTGT GTGTTCCTGG 1740
AGTTAGGCAT CATCTTGGTT TTTACTCCCT TGCTTGGTTT TCTCAGGATC TCTGGCTGCT 1800
CCGTCCTTGC TCCAGCGTTC TTCTCTGCCC CCTCCCTCTG TGGTCCAGAG GCCGATGGCC 1860
AGCTGGCCCT CACCTGCCCG CCCTGGGTAT TTCTGTGCTC TTCCTGGTGA GGGATTCTAG 1920
GGGTTCCCCT CCTGGGTTCA TCCTTACCTG AGTAGCCACA GCACACTGTG CAGTTGGGTG 1980
CCTGGGAGGC ACGTGCTTTG GGTGTTGCAT GGCTGACCTG GTAACTGGGC ACCCGTGTAT 2040
GGAGGGCTGG AACAGAACAC TTGTCGGCGC TCCTCAGCGT CTTGCCTCTG GTGTCCCCAT 2100
GGCGAAGTCC CCTGCCATCT GCTTTGGGCT CTGACATGTG ACCTGACTGT GCCCTTCAGG 2160
AGCTTTCAGA ACCTCCTCTT AGATCTGGCA TTCAAAATGT CTTGTCAGAC ACCTCGAGGC 2220
GGCTTGTGTT TGGCCCTGTG TTGGGCGCCT ATTGGGCCCT TGTCAGGTTT TTGTTGCCAG 2280
GAGGCTCGCG CCCCGATCTT CGGGATGGTG CCCGTGGCAT CTTCTGCTCG GTGCTCCCTA 2340
GGGCTGGACG TTGGTCCTCC TGGCACTGGT GCTCCGGTTG CTGTGGTCTC CCTGCTGTTC 2400
CCTTGTGGCT CAGGATTACT CTCTGGAGGT CTCCGCCTTA TCATGAGCAC TTTCTTTGTT 2460
GGCTACTTTT AGTTTCATGA TTTCATTTTC GTTTCTAAGA TATCTATCTC TTTGTAAAAG 2520
CTCCCACCTT TTGTGACTTG TGGATGCTGT ATCTTTCTCC TGTTGCTGCA GACATTAATG 2580
ATGTTTTTCT TGACAGTTTG TCCTGCTGGT TTCCTCTGCA TTCCTTTGGT TGGTTTCAGA 2640
CCTCGGCTTT AAAGGGGCAT TTCCCCACAT TGCCAATTCT TGACCATCTG GTCACGTCAA 2700
GGCTGACGTG CCAATGGCTG CAAGGGGGAG GGCACCTGGG AGCCCGCGGA TGGCTCTTAT 2760
GCAGACGTGC GGGCCAGCCC CGATCCTGCT TCTGCAAGGC CTCCCCTCCC ATGGTGGCGC 2820
TTTGGTGCCA GAGCGCGTCG GCGTGGCTCC CTAGCGTCTG CCTCTGCAGC TGCTTGGCCC 2880
CCAGCCGCCT CCTCCCAGCT GCCTCCTGCC CTATGTGTGC TTGAGCTCGA GACAATGCTT 2940
CCTTCATCCA AGAGCCGGGC TCTCGGCGAT TTTTGAGAGG AGAATGGGGT TGAAGCGATG 3000
TTGCTCTTCC GTCTTAAAAC TGGATTTCTT TCCTCATGCT 3040