EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-00038 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr1:2186280-2188920 
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
TGCGGTCAGG TGAGCTCTGG GGGGTTTCTG AGGGTGGAGA CAGCCACAAC AACACTTCTT 60
TCCTCCAAAT GCCTGTGCTG TGCACTTGGG TGCAGGTGGC TTTTAGGGGA CATGGCTGGG 120
CACTGCCCCA CAGTGTCACC TCTGTGTCCT GTGGTGCGTG CTGTGGACTG GCACCACACC 180
CCACGTGCTT GTTAGGCCAG TTTCTCTCAG GTGTCGGTCA CCCTACCATG CGGCCTTTCT 240
TTTGTCTTTT ATCTTTAGCT AAGGAGTCCA TGGCATACCA AAAGCTGAAT GATGACAGCC 300
AGTGTCCCCA TCCTGTCCTC CCCAACTTTC CACAGGCAGG GACGCTCCCC ATTCTTGCTG 360
CATAGTCTTC TGTTGACCCC ATGTACCTGA GTGACCCCCA CGTACCTGAG TGTGACAAGC 420
ACTATGGTGC TTGACCTCAG TCCAGCTGCT TAGACCTGTA CCTGCCACAG CCCCACGTGC 480
TGACACCTTG CGTCTTGAGT TTTGATAAAT CTATCCTTTG GCTGATTAAT ATGACTGAGT 540
GGTGTCTTCT GACCCCATTT CTTATCTGGA ACACTGTGTC CTGACTTCAT TTCCTGTCTG 600
GAGCACACTG TCCTGACCTC ATTTCCTGTC TGGAACACAC TGTGTCCTGA CCTCATTTCC 660
TGCCTGGAGC TCTCTGTGTC CTGACCTCAT TTCCTGTCTG TGCCGCTCTG TCCTGACCTC 720
ATTTTCTGTC TGTGCCACCC TTTGTCCTGA CCTCATTTCC TGTCTGGAAC ATGCTGTGTC 780
CTAACTGCAT TTCCTGTCTG GAGCTCTCTC TGTCCTGACC TCATTTCCTG TCTGGATCTC 840
TCTATGTCCT GACCTCATTT CCTGTCTGGA ACATGCTGTA TCCTGATATC ATTTCCTGTC 900
TGTGCCACTT TGTCCGGACC TCATTTTCTG TCTGGAGCAC TCTGTATCCT GACCTCATTT 960
CCTGTTTGTG CCACCCTTTG TCCTGACCTC ATTTCCTGTC TGGAACATGC TGTGTCCGGA 1020
TTGCATTTCC TCTCTGGAGC TCTCTCTGTC CTGACCTCAT TTCCTGTCTG GAGCCAGTGA 1080
CCTCATTTCC TGTCTGTGTC ACTCTGTCCT GACCTCATTT CCTGTCTGTG CCACTCTTTG 1140
TCCTGACCTC ATTTCCTGTA TGCAACACAC TGTGCCCGGA CTGCATTTCC TGTCTGGAGC 1200
TCTCTCTGTC CTGATCTCAT TTCCTGTCAG GAGCACTCTG TGTACTGACC TCATTTCCTG 1260
TCTGTGCCAC TCTTGTGTCC TGACCTCTTT TCCAGTCTGT GCCACTCTGT GTCCTGACCT 1320
CATTTCTTAT CTGTGCCACT CTGTGTCCTG ACCTCATTTC CTGTCTGGAG CACTCTGTCC 1380
TGACCTCATT TCCTGTCTTG TGTCCTGACC TCATTTCCTG TCTGGAGCTC TCTGTGTCCT 1440
TACCTCATTT CCTGTCTGTG CTGCTTTCTG TCTTGGAGTT GCGTGCCTGA CCTCATTTCC 1500
TCTCCACTGT GTGTTCCTGG AGTTAGGCAT CATCTTGGTT TTTACTCCCT TGCTTGGTTT 1560
TCTCAGGATC TCTGGCTGCT CCGTCCTTGC TCCAGCGTTC TTCTCTGCCC CCTCCCTCTG 1620
TGGTCCAGAG GCCGATGGCC AGCTGGCCCT CACCTGCCCG CCCTGGGTAT TTCTGTGCTC 1680
TTCCTGGTGA GGGATTCTAG GGGTTCCCCT CCTGGGTTCA TCCTTACCTG AGTAGCCACA 1740
GCACACTGTG CAGTTGGGTG CCTGGGAGGC ACGTGCTTTG GGTGTTGCAT GGCTGACCTG 1800
GTAACTGGGC ACCCGTGTAT GGAGGGCTGG AACAGAACAC TTGTCGGCGC TCCTCAGCGT 1860
CTTGCCTCTG GTGTCCCCAT GGCGAAGTCC CCTGCCATCT GCTTTGGGCT CTGACATGTG 1920
ACCTGACTGT GCCCTTCAGG AGCTTTCAGA ACCTCCTCTT AGATCTGGCA TTCAAAATGT 1980
CTTGTCAGAC ACCTCGAGGC GGCTTGTGTT TGGCCCTGTG TTGGGCGCCT ATTGGGCCCT 2040
TGTCAGGTTT TTGTTGCCAG GAGGCTCGCG CCCCGATCTT CGGGATGGTG CCCGTGGCAT 2100
CTTCTGCTCG GTGCTCCCTA GGGCTGGACG TTGGTCCTCC TGGCACTGGT GCTCCGGTTG 2160
CTGTGGTCTC CCTGCTGTTC CCTTGTGGCT CAGGATTACT CTCTGGAGGT CTCCGCCTTA 2220
TCATGAGCAC TTTCTTTGTT GGCTACTTTT AGTTTCATGA TTTCATTTTC GTTTCTAAGA 2280
TATCTATCTC TTTGTAAAAG CTCCCACCTT TTGTGACTTG TGGATGCTGT ATCTTTCTCC 2340
TGTTGCTGCA GACATTAATG ATGTTTTTCT TGACAGTTTG TCCTGCTGGT TTCCTCTGCA 2400
TTCCTTTGGT TGGTTTCAGA CCTCGGCTTT AAAGGGGCAT TTCCCCACAT TGCCAATTCT 2460
TGACCATCTG GTCACGTCAA GGCTGACGTG CCAATGGCTG CAAGGGGGAG GGCACCTGGG 2520
AGCCCGCGGA TGGCTCTTAT GCAGACGTGC GGGCCAGCCC CGATCCTGCT TCTGCAAGGC 2580
CTCCCCTCCC ATGGTGGCGC TTTGGTGCCA GAGCGCGTCG GCGTGGCTCC CTAGCGTCTG 2640