EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS190-00020 
Organism
Homo sapiens 
Tissue/cell
Treg_cell 
Coordinate
chr1:2186140-2188960 
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: 25             
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_08969chr1:2188435-2188720Brain_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
ACAGTCTTGG CCAGACTGTG GTCACTGCGT GCGTGTGTGT GTGTGTGTGA TGCGCAGGGC 60
ATTTGCTGGT GGAATAGCAC GGGCCATTGG CATTTGCACC TGAGGCGTGC AGCCCCCCTG 120
CTGCACACCT ATGGGGTCCC TGCGGTCAGG TGAGCTCTGG GGGGTTTCTG AGGGTGGAGA 180
CAGCCACAAC AACACTTCTT TCCTCCAAAT GCCTGTGCTG TGCACTTGGG TGCAGGTGGC 240
TTTTAGGGGA CATGGCTGGG CACTGCCCCA CAGTGTCACC TCTGTGTCCT GTGGTGCGTG 300
CTGTGGACTG GCACCACACC CCACGTGCTT GTTAGGCCAG TTTCTCTCAG GTGTCGGTCA 360
CCCTACCATG CGGCCTTTCT TTTGTCTTTT ATCTTTAGCT AAGGAGTCCA TGGCATACCA 420
AAAGCTGAAT GATGACAGCC AGTGTCCCCA TCCTGTCCTC CCCAACTTTC CACAGGCAGG 480
GACGCTCCCC ATTCTTGCTG CATAGTCTTC TGTTGACCCC ATGTACCTGA GTGACCCCCA 540
CGTACCTGAG TGTGACAAGC ACTATGGTGC TTGACCTCAG TCCAGCTGCT TAGACCTGTA 600
CCTGCCACAG CCCCACGTGC TGACACCTTG CGTCTTGAGT TTTGATAAAT CTATCCTTTG 660
GCTGATTAAT ATGACTGAGT GGTGTCTTCT GACCCCATTT CTTATCTGGA ACACTGTGTC 720
CTGACTTCAT TTCCTGTCTG GAGCACACTG TCCTGACCTC ATTTCCTGTC TGGAACACAC 780
TGTGTCCTGA CCTCATTTCC TGCCTGGAGC TCTCTGTGTC CTGACCTCAT TTCCTGTCTG 840
TGCCGCTCTG TCCTGACCTC ATTTTCTGTC TGTGCCACCC TTTGTCCTGA CCTCATTTCC 900
TGTCTGGAAC ATGCTGTGTC CTAACTGCAT TTCCTGTCTG GAGCTCTCTC TGTCCTGACC 960
TCATTTCCTG TCTGGATCTC TCTATGTCCT GACCTCATTT CCTGTCTGGA ACATGCTGTA 1020
TCCTGATATC ATTTCCTGTC TGTGCCACTT TGTCCGGACC TCATTTTCTG TCTGGAGCAC 1080
TCTGTATCCT GACCTCATTT CCTGTTTGTG CCACCCTTTG TCCTGACCTC ATTTCCTGTC 1140
TGGAACATGC TGTGTCCGGA TTGCATTTCC TCTCTGGAGC TCTCTCTGTC CTGACCTCAT 1200
TTCCTGTCTG GAGCCAGTGA CCTCATTTCC TGTCTGTGTC ACTCTGTCCT GACCTCATTT 1260
CCTGTCTGTG CCACTCTTTG TCCTGACCTC ATTTCCTGTA TGCAACACAC TGTGCCCGGA 1320
CTGCATTTCC TGTCTGGAGC TCTCTCTGTC CTGATCTCAT TTCCTGTCAG GAGCACTCTG 1380
TGTACTGACC TCATTTCCTG TCTGTGCCAC TCTTGTGTCC TGACCTCTTT TCCAGTCTGT 1440
GCCACTCTGT GTCCTGACCT CATTTCTTAT CTGTGCCACT CTGTGTCCTG ACCTCATTTC 1500
CTGTCTGGAG CACTCTGTCC TGACCTCATT TCCTGTCTTG TGTCCTGACC TCATTTCCTG 1560
TCTGGAGCTC TCTGTGTCCT TACCTCATTT CCTGTCTGTG CTGCTTTCTG TCTTGGAGTT 1620
GCGTGCCTGA CCTCATTTCC TCTCCACTGT GTGTTCCTGG AGTTAGGCAT CATCTTGGTT 1680
TTTACTCCCT TGCTTGGTTT TCTCAGGATC TCTGGCTGCT CCGTCCTTGC TCCAGCGTTC 1740
TTCTCTGCCC CCTCCCTCTG TGGTCCAGAG GCCGATGGCC AGCTGGCCCT CACCTGCCCG 1800
CCCTGGGTAT TTCTGTGCTC TTCCTGGTGA GGGATTCTAG GGGTTCCCCT CCTGGGTTCA 1860
TCCTTACCTG AGTAGCCACA GCACACTGTG CAGTTGGGTG CCTGGGAGGC ACGTGCTTTG 1920
GGTGTTGCAT GGCTGACCTG GTAACTGGGC ACCCGTGTAT GGAGGGCTGG AACAGAACAC 1980
TTGTCGGCGC TCCTCAGCGT CTTGCCTCTG GTGTCCCCAT GGCGAAGTCC CCTGCCATCT 2040
GCTTTGGGCT CTGACATGTG ACCTGACTGT GCCCTTCAGG AGCTTTCAGA ACCTCCTCTT 2100
AGATCTGGCA TTCAAAATGT CTTGTCAGAC ACCTCGAGGC GGCTTGTGTT TGGCCCTGTG 2160
TTGGGCGCCT ATTGGGCCCT TGTCAGGTTT TTGTTGCCAG GAGGCTCGCG CCCCGATCTT 2220
CGGGATGGTG CCCGTGGCAT CTTCTGCTCG GTGCTCCCTA GGGCTGGACG TTGGTCCTCC 2280
TGGCACTGGT GCTCCGGTTG CTGTGGTCTC CCTGCTGTTC CCTTGTGGCT CAGGATTACT 2340
CTCTGGAGGT CTCCGCCTTA TCATGAGCAC TTTCTTTGTT GGCTACTTTT AGTTTCATGA 2400
TTTCATTTTC GTTTCTAAGA TATCTATCTC TTTGTAAAAG CTCCCACCTT TTGTGACTTG 2460
TGGATGCTGT ATCTTTCTCC TGTTGCTGCA GACATTAATG ATGTTTTTCT TGACAGTTTG 2520
TCCTGCTGGT TTCCTCTGCA TTCCTTTGGT TGGTTTCAGA CCTCGGCTTT AAAGGGGCAT 2580
TTCCCCACAT TGCCAATTCT TGACCATCTG GTCACGTCAA GGCTGACGTG CCAATGGCTG 2640
CAAGGGGGAG GGCACCTGGG AGCCCGCGGA TGGCTCTTAT GCAGACGTGC GGGCCAGCCC 2700
CGATCCTGCT TCTGCAAGGC CTCCCCTCCC ATGGTGGCGC TTTGGTGCCA GAGCGCGTCG 2760
GCGTGGCTCC CTAGCGTCTG CCTCTGCAGC TGCTTGGCCC CCAGCCGCCT CCTCCCAGCT 2820