EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-00109 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr1:2186000-2188490 
Target genes
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
TGTCCTTGTG TGCAGTGACC GGTCTACCTG TCTGGCCTTG TGCCTAGACT TGTGGCCGTC 60
ACCACTATCT CTGGGGAGGG GTGAAGTGGA CTGGGAGGTA GGAGCCGAAT TGGAGTCTTC 120
TCTTTGTTCC TGAAGTTATC ACAGTCTTGG CCAGACTGTG GTCACTGCGT GCGTGTGTGT 180
GTGTGTGTGA TGCGCAGGGC ATTTGCTGGT GGAATAGCAC GGGCCATTGG CATTTGCACC 240
TGAGGCGTGC AGCCCCCCTG CTGCACACCT ATGGGGTCCC TGCGGTCAGG TGAGCTCTGG 300
GGGGTTTCTG AGGGTGGAGA CAGCCACAAC AACACTTCTT TCCTCCAAAT GCCTGTGCTG 360
TGCACTTGGG TGCAGGTGGC TTTTAGGGGA CATGGCTGGG CACTGCCCCA CAGTGTCACC 420
TCTGTGTCCT GTGGTGCGTG CTGTGGACTG GCACCACACC CCACGTGCTT GTTAGGCCAG 480
TTTCTCTCAG GTGTCGGTCA CCCTACCATG CGGCCTTTCT TTTGTCTTTT ATCTTTAGCT 540
AAGGAGTCCA TGGCATACCA AAAGCTGAAT GATGACAGCC AGTGTCCCCA TCCTGTCCTC 600
CCCAACTTTC CACAGGCAGG GACGCTCCCC ATTCTTGCTG CATAGTCTTC TGTTGACCCC 660
ATGTACCTGA GTGACCCCCA CGTACCTGAG TGTGACAAGC ACTATGGTGC TTGACCTCAG 720
TCCAGCTGCT TAGACCTGTA CCTGCCACAG CCCCACGTGC TGACACCTTG CGTCTTGAGT 780
TTTGATAAAT CTATCCTTTG GCTGATTAAT ATGACTGAGT GGTGTCTTCT GACCCCATTT 840
CTTATCTGGA ACACTGTGTC CTGACTTCAT TTCCTGTCTG GAGCACACTG TCCTGACCTC 900
ATTTCCTGTC TGGAACACAC TGTGTCCTGA CCTCATTTCC TGCCTGGAGC TCTCTGTGTC 960
CTGACCTCAT TTCCTGTCTG TGCCGCTCTG TCCTGACCTC ATTTTCTGTC TGTGCCACCC 1020
TTTGTCCTGA CCTCATTTCC TGTCTGGAAC ATGCTGTGTC CTAACTGCAT TTCCTGTCTG 1080
GAGCTCTCTC TGTCCTGACC TCATTTCCTG TCTGGATCTC TCTATGTCCT GACCTCATTT 1140
CCTGTCTGGA ACATGCTGTA TCCTGATATC ATTTCCTGTC TGTGCCACTT TGTCCGGACC 1200
TCATTTTCTG TCTGGAGCAC TCTGTATCCT GACCTCATTT CCTGTTTGTG CCACCCTTTG 1260
TCCTGACCTC ATTTCCTGTC TGGAACATGC TGTGTCCGGA TTGCATTTCC TCTCTGGAGC 1320
TCTCTCTGTC CTGACCTCAT TTCCTGTCTG GAGCCAGTGA CCTCATTTCC TGTCTGTGTC 1380
ACTCTGTCCT GACCTCATTT CCTGTCTGTG CCACTCTTTG TCCTGACCTC ATTTCCTGTA 1440
TGCAACACAC TGTGCCCGGA CTGCATTTCC TGTCTGGAGC TCTCTCTGTC CTGATCTCAT 1500
TTCCTGTCAG GAGCACTCTG TGTACTGACC TCATTTCCTG TCTGTGCCAC TCTTGTGTCC 1560
TGACCTCTTT TCCAGTCTGT GCCACTCTGT GTCCTGACCT CATTTCTTAT CTGTGCCACT 1620
CTGTGTCCTG ACCTCATTTC CTGTCTGGAG CACTCTGTCC TGACCTCATT TCCTGTCTTG 1680
TGTCCTGACC TCATTTCCTG TCTGGAGCTC TCTGTGTCCT TACCTCATTT CCTGTCTGTG 1740
CTGCTTTCTG TCTTGGAGTT GCGTGCCTGA CCTCATTTCC TCTCCACTGT GTGTTCCTGG 1800
AGTTAGGCAT CATCTTGGTT TTTACTCCCT TGCTTGGTTT TCTCAGGATC TCTGGCTGCT 1860
CCGTCCTTGC TCCAGCGTTC TTCTCTGCCC CCTCCCTCTG TGGTCCAGAG GCCGATGGCC 1920
AGCTGGCCCT CACCTGCCCG CCCTGGGTAT TTCTGTGCTC TTCCTGGTGA GGGATTCTAG 1980
GGGTTCCCCT CCTGGGTTCA TCCTTACCTG AGTAGCCACA GCACACTGTG CAGTTGGGTG 2040
CCTGGGAGGC ACGTGCTTTG GGTGTTGCAT GGCTGACCTG GTAACTGGGC ACCCGTGTAT 2100
GGAGGGCTGG AACAGAACAC TTGTCGGCGC TCCTCAGCGT CTTGCCTCTG GTGTCCCCAT 2160
GGCGAAGTCC CCTGCCATCT GCTTTGGGCT CTGACATGTG ACCTGACTGT GCCCTTCAGG 2220
AGCTTTCAGA ACCTCCTCTT AGATCTGGCA TTCAAAATGT CTTGTCAGAC ACCTCGAGGC 2280
GGCTTGTGTT TGGCCCTGTG TTGGGCGCCT ATTGGGCCCT TGTCAGGTTT TTGTTGCCAG 2340
GAGGCTCGCG CCCCGATCTT CGGGATGGTG CCCGTGGCAT CTTCTGCTCG GTGCTCCCTA 2400
GGGCTGGACG TTGGTCCTCC TGGCACTGGT GCTCCGGTTG CTGTGGTCTC CCTGCTGTTC 2460
CCTTGTGGCT CAGGATTACT CTCTGGAGGT 2490