EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS029-00042 
Organism
Homo sapiens 
Tissue/cell
CUTLL1 
Coordinate
chr1:2185640-2188610 
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
TGAAGAATCT GGAAGGTCCA CGCTAGAGGA GGCCACGACC TGCTGGTGCG CCTGCAAGAG 60
TGCTGGCCCA ACTGGTCTCC ATGCGTGGTG CCCGTTGGAG GGGGTGGGAG GGCTCGGCTC 120
TGCTCTCCCC CCGTGGGTCT TCGTGTCACA GGGTGCTTGG GGGACTCTGC TGCACTGAGA 180
TCTCCAGCGT GACATGTCCC CGTCCCAAAC AGCCCTGAAA TGGCAATGCC TCATCCTAGG 240
ATTACCGTCC CTTCCCGAAG GCTTGAGGTC CTACTTAGAT GTCTACTGGA CTGCTTTTTA 300
TTTTAATTTA CTTGATACTC AGTCTGGGTG CGTTGAAGAC GCGGCCTCTG GCTGTCAGCC 360
TGTCCTTGTG TGCAGTGACC GGTCTACCTG TCTGGCCTTG TGCCTAGACT TGTGGCCGTC 420
ACCACTATCT CTGGGGAGGG GTGAAGTGGA CTGGGAGGTA GGAGCCGAAT TGGAGTCTTC 480
TCTTTGTTCC TGAAGTTATC ACAGTCTTGG CCAGACTGTG GTCACTGCGT GCGTGTGTGT 540
GTGTGTGTGA TGCGCAGGGC ATTTGCTGGT GGAATAGCAC GGGCCATTGG CATTTGCACC 600
TGAGGCGTGC AGCCCCCCTG CTGCACACCT ATGGGGTCCC TGCGGTCAGG TGAGCTCTGG 660
GGGGTTTCTG AGGGTGGAGA CAGCCACAAC AACACTTCTT TCCTCCAAAT GCCTGTGCTG 720
TGCACTTGGG TGCAGGTGGC TTTTAGGGGA CATGGCTGGG CACTGCCCCA CAGTGTCACC 780
TCTGTGTCCT GTGGTGCGTG CTGTGGACTG GCACCACACC CCACGTGCTT GTTAGGCCAG 840
TTTCTCTCAG GTGTCGGTCA CCCTACCATG CGGCCTTTCT TTTGTCTTTT ATCTTTAGCT 900
AAGGAGTCCA TGGCATACCA AAAGCTGAAT GATGACAGCC AGTGTCCCCA TCCTGTCCTC 960
CCCAACTTTC CACAGGCAGG GACGCTCCCC ATTCTTGCTG CATAGTCTTC TGTTGACCCC 1020
ATGTACCTGA GTGACCCCCA CGTACCTGAG TGTGACAAGC ACTATGGTGC TTGACCTCAG 1080
TCCAGCTGCT TAGACCTGTA CCTGCCACAG CCCCACGTGC TGACACCTTG CGTCTTGAGT 1140
TTTGATAAAT CTATCCTTTG GCTGATTAAT ATGACTGAGT GGTGTCTTCT GACCCCATTT 1200
CTTATCTGGA ACACTGTGTC CTGACTTCAT TTCCTGTCTG GAGCACACTG TCCTGACCTC 1260
ATTTCCTGTC TGGAACACAC TGTGTCCTGA CCTCATTTCC TGCCTGGAGC TCTCTGTGTC 1320
CTGACCTCAT TTCCTGTCTG TGCCGCTCTG TCCTGACCTC ATTTTCTGTC TGTGCCACCC 1380
TTTGTCCTGA CCTCATTTCC TGTCTGGAAC ATGCTGTGTC CTAACTGCAT TTCCTGTCTG 1440
GAGCTCTCTC TGTCCTGACC TCATTTCCTG TCTGGATCTC TCTATGTCCT GACCTCATTT 1500
CCTGTCTGGA ACATGCTGTA TCCTGATATC ATTTCCTGTC TGTGCCACTT TGTCCGGACC 1560
TCATTTTCTG TCTGGAGCAC TCTGTATCCT GACCTCATTT CCTGTTTGTG CCACCCTTTG 1620
TCCTGACCTC ATTTCCTGTC TGGAACATGC TGTGTCCGGA TTGCATTTCC TCTCTGGAGC 1680
TCTCTCTGTC CTGACCTCAT TTCCTGTCTG GAGCCAGTGA CCTCATTTCC TGTCTGTGTC 1740
ACTCTGTCCT GACCTCATTT CCTGTCTGTG CCACTCTTTG TCCTGACCTC ATTTCCTGTA 1800
TGCAACACAC TGTGCCCGGA CTGCATTTCC TGTCTGGAGC TCTCTCTGTC CTGATCTCAT 1860
TTCCTGTCAG GAGCACTCTG TGTACTGACC TCATTTCCTG TCTGTGCCAC TCTTGTGTCC 1920
TGACCTCTTT TCCAGTCTGT GCCACTCTGT GTCCTGACCT CATTTCTTAT CTGTGCCACT 1980
CTGTGTCCTG ACCTCATTTC CTGTCTGGAG CACTCTGTCC TGACCTCATT TCCTGTCTTG 2040
TGTCCTGACC TCATTTCCTG TCTGGAGCTC TCTGTGTCCT TACCTCATTT CCTGTCTGTG 2100
CTGCTTTCTG TCTTGGAGTT GCGTGCCTGA CCTCATTTCC TCTCCACTGT GTGTTCCTGG 2160
AGTTAGGCAT CATCTTGGTT TTTACTCCCT TGCTTGGTTT TCTCAGGATC TCTGGCTGCT 2220
CCGTCCTTGC TCCAGCGTTC TTCTCTGCCC CCTCCCTCTG TGGTCCAGAG GCCGATGGCC 2280
AGCTGGCCCT CACCTGCCCG CCCTGGGTAT TTCTGTGCTC TTCCTGGTGA GGGATTCTAG 2340
GGGTTCCCCT CCTGGGTTCA TCCTTACCTG AGTAGCCACA GCACACTGTG CAGTTGGGTG 2400
CCTGGGAGGC ACGTGCTTTG GGTGTTGCAT GGCTGACCTG GTAACTGGGC ACCCGTGTAT 2460
GGAGGGCTGG AACAGAACAC TTGTCGGCGC TCCTCAGCGT CTTGCCTCTG GTGTCCCCAT 2520
GGCGAAGTCC CCTGCCATCT GCTTTGGGCT CTGACATGTG ACCTGACTGT GCCCTTCAGG 2580
AGCTTTCAGA ACCTCCTCTT AGATCTGGCA TTCAAAATGT CTTGTCAGAC ACCTCGAGGC 2640
GGCTTGTGTT TGGCCCTGTG TTGGGCGCCT ATTGGGCCCT TGTCAGGTTT TTGTTGCCAG 2700
GAGGCTCGCG CCCCGATCTT CGGGATGGTG CCCGTGGCAT CTTCTGCTCG GTGCTCCCTA 2760
GGGCTGGACG TTGGTCCTCC TGGCACTGGT GCTCCGGTTG CTGTGGTCTC CCTGCTGTTC 2820
CCTTGTGGCT CAGGATTACT CTCTGGAGGT CTCCGCCTTA TCATGAGCAC TTTCTTTGTT 2880
GGCTACTTTT AGTTTCATGA TTTCATTTTC GTTTCTAAGA TATCTATCTC TTTGTAAAAG 2940
CTCCCACCTT TTGTGACTTG TGGATGCTGT 2970