EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS136-00027 
Organism
Homo sapiens 
Tissue/cell
Monocyte 
Coordinate
chr1:2185800-2188860 
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_05718chr1:2184573-2186113Brain_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
GGGACTCTGC TGCACTGAGA TCTCCAGCGT GACATGTCCC CGTCCCAAAC AGCCCTGAAA 60
TGGCAATGCC TCATCCTAGG ATTACCGTCC CTTCCCGAAG GCTTGAGGTC CTACTTAGAT 120
GTCTACTGGA CTGCTTTTTA TTTTAATTTA CTTGATACTC AGTCTGGGTG CGTTGAAGAC 180
GCGGCCTCTG GCTGTCAGCC TGTCCTTGTG TGCAGTGACC GGTCTACCTG TCTGGCCTTG 240
TGCCTAGACT TGTGGCCGTC ACCACTATCT CTGGGGAGGG GTGAAGTGGA CTGGGAGGTA 300
GGAGCCGAAT TGGAGTCTTC TCTTTGTTCC TGAAGTTATC ACAGTCTTGG CCAGACTGTG 360
GTCACTGCGT GCGTGTGTGT GTGTGTGTGA TGCGCAGGGC ATTTGCTGGT GGAATAGCAC 420
GGGCCATTGG CATTTGCACC TGAGGCGTGC AGCCCCCCTG CTGCACACCT ATGGGGTCCC 480
TGCGGTCAGG TGAGCTCTGG GGGGTTTCTG AGGGTGGAGA CAGCCACAAC AACACTTCTT 540
TCCTCCAAAT GCCTGTGCTG TGCACTTGGG TGCAGGTGGC TTTTAGGGGA CATGGCTGGG 600
CACTGCCCCA CAGTGTCACC TCTGTGTCCT GTGGTGCGTG CTGTGGACTG GCACCACACC 660
CCACGTGCTT GTTAGGCCAG TTTCTCTCAG GTGTCGGTCA CCCTACCATG CGGCCTTTCT 720
TTTGTCTTTT ATCTTTAGCT AAGGAGTCCA TGGCATACCA AAAGCTGAAT GATGACAGCC 780
AGTGTCCCCA TCCTGTCCTC CCCAACTTTC CACAGGCAGG GACGCTCCCC ATTCTTGCTG 840
CATAGTCTTC TGTTGACCCC ATGTACCTGA GTGACCCCCA CGTACCTGAG TGTGACAAGC 900
ACTATGGTGC TTGACCTCAG TCCAGCTGCT TAGACCTGTA CCTGCCACAG CCCCACGTGC 960
TGACACCTTG CGTCTTGAGT TTTGATAAAT CTATCCTTTG GCTGATTAAT ATGACTGAGT 1020
GGTGTCTTCT GACCCCATTT CTTATCTGGA ACACTGTGTC CTGACTTCAT TTCCTGTCTG 1080
GAGCACACTG TCCTGACCTC ATTTCCTGTC TGGAACACAC TGTGTCCTGA CCTCATTTCC 1140
TGCCTGGAGC TCTCTGTGTC CTGACCTCAT TTCCTGTCTG TGCCGCTCTG TCCTGACCTC 1200
ATTTTCTGTC TGTGCCACCC TTTGTCCTGA CCTCATTTCC TGTCTGGAAC ATGCTGTGTC 1260
CTAACTGCAT TTCCTGTCTG GAGCTCTCTC TGTCCTGACC TCATTTCCTG TCTGGATCTC 1320
TCTATGTCCT GACCTCATTT CCTGTCTGGA ACATGCTGTA TCCTGATATC ATTTCCTGTC 1380
TGTGCCACTT TGTCCGGACC TCATTTTCTG TCTGGAGCAC TCTGTATCCT GACCTCATTT 1440
CCTGTTTGTG CCACCCTTTG TCCTGACCTC ATTTCCTGTC TGGAACATGC TGTGTCCGGA 1500
TTGCATTTCC TCTCTGGAGC TCTCTCTGTC CTGACCTCAT TTCCTGTCTG GAGCCAGTGA 1560
CCTCATTTCC TGTCTGTGTC ACTCTGTCCT GACCTCATTT CCTGTCTGTG CCACTCTTTG 1620
TCCTGACCTC ATTTCCTGTA TGCAACACAC TGTGCCCGGA CTGCATTTCC TGTCTGGAGC 1680
TCTCTCTGTC CTGATCTCAT TTCCTGTCAG GAGCACTCTG TGTACTGACC TCATTTCCTG 1740
TCTGTGCCAC TCTTGTGTCC TGACCTCTTT TCCAGTCTGT GCCACTCTGT GTCCTGACCT 1800
CATTTCTTAT CTGTGCCACT CTGTGTCCTG ACCTCATTTC CTGTCTGGAG CACTCTGTCC 1860
TGACCTCATT TCCTGTCTTG TGTCCTGACC TCATTTCCTG TCTGGAGCTC TCTGTGTCCT 1920
TACCTCATTT CCTGTCTGTG CTGCTTTCTG TCTTGGAGTT GCGTGCCTGA CCTCATTTCC 1980
TCTCCACTGT GTGTTCCTGG AGTTAGGCAT CATCTTGGTT TTTACTCCCT TGCTTGGTTT 2040
TCTCAGGATC TCTGGCTGCT CCGTCCTTGC TCCAGCGTTC TTCTCTGCCC CCTCCCTCTG 2100
TGGTCCAGAG GCCGATGGCC AGCTGGCCCT CACCTGCCCG CCCTGGGTAT TTCTGTGCTC 2160
TTCCTGGTGA GGGATTCTAG GGGTTCCCCT CCTGGGTTCA TCCTTACCTG AGTAGCCACA 2220
GCACACTGTG CAGTTGGGTG CCTGGGAGGC ACGTGCTTTG GGTGTTGCAT GGCTGACCTG 2280
GTAACTGGGC ACCCGTGTAT GGAGGGCTGG AACAGAACAC TTGTCGGCGC TCCTCAGCGT 2340
CTTGCCTCTG GTGTCCCCAT GGCGAAGTCC CCTGCCATCT GCTTTGGGCT CTGACATGTG 2400
ACCTGACTGT GCCCTTCAGG AGCTTTCAGA ACCTCCTCTT AGATCTGGCA TTCAAAATGT 2460
CTTGTCAGAC ACCTCGAGGC GGCTTGTGTT TGGCCCTGTG TTGGGCGCCT ATTGGGCCCT 2520
TGTCAGGTTT TTGTTGCCAG GAGGCTCGCG CCCCGATCTT CGGGATGGTG CCCGTGGCAT 2580
CTTCTGCTCG GTGCTCCCTA GGGCTGGACG TTGGTCCTCC TGGCACTGGT GCTCCGGTTG 2640
CTGTGGTCTC CCTGCTGTTC CCTTGTGGCT CAGGATTACT CTCTGGAGGT CTCCGCCTTA 2700
TCATGAGCAC TTTCTTTGTT GGCTACTTTT AGTTTCATGA TTTCATTTTC GTTTCTAAGA 2760
TATCTATCTC TTTGTAAAAG CTCCCACCTT TTGTGACTTG TGGATGCTGT ATCTTTCTCC 2820
TGTTGCTGCA GACATTAATG ATGTTTTTCT TGACAGTTTG TCCTGCTGGT TTCCTCTGCA 2880
TTCCTTTGGT TGGTTTCAGA CCTCGGCTTT AAAGGGGCAT TTCCCCACAT TGCCAATTCT 2940
TGACCATCTG GTCACGTCAA GGCTGACGTG CCAATGGCTG CAAGGGGGAG GGCACCTGGG 3000
AGCCCGCGGA TGGCTCTTAT GCAGACGTGC GGGCCAGCCC CGATCCTGCT TCTGCAAGGC 3060