EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-00076 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:2185930-2189060 
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: 24             
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_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
CTGCTTTTTA TTTTAATTTA CTTGATACTC AGTCTGGGTG CGTTGAAGAC GCGGCCTCTG 60
GCTGTCAGCC TGTCCTTGTG TGCAGTGACC GGTCTACCTG TCTGGCCTTG TGCCTAGACT 120
TGTGGCCGTC ACCACTATCT CTGGGGAGGG GTGAAGTGGA CTGGGAGGTA GGAGCCGAAT 180
TGGAGTCTTC TCTTTGTTCC TGAAGTTATC ACAGTCTTGG CCAGACTGTG GTCACTGCGT 240
GCGTGTGTGT GTGTGTGTGA TGCGCAGGGC ATTTGCTGGT GGAATAGCAC GGGCCATTGG 300
CATTTGCACC TGAGGCGTGC AGCCCCCCTG CTGCACACCT ATGGGGTCCC TGCGGTCAGG 360
TGAGCTCTGG GGGGTTTCTG AGGGTGGAGA CAGCCACAAC AACACTTCTT TCCTCCAAAT 420
GCCTGTGCTG TGCACTTGGG TGCAGGTGGC TTTTAGGGGA CATGGCTGGG CACTGCCCCA 480
CAGTGTCACC TCTGTGTCCT GTGGTGCGTG CTGTGGACTG GCACCACACC CCACGTGCTT 540
GTTAGGCCAG TTTCTCTCAG GTGTCGGTCA CCCTACCATG CGGCCTTTCT TTTGTCTTTT 600
ATCTTTAGCT AAGGAGTCCA TGGCATACCA AAAGCTGAAT GATGACAGCC AGTGTCCCCA 660
TCCTGTCCTC CCCAACTTTC CACAGGCAGG GACGCTCCCC ATTCTTGCTG CATAGTCTTC 720
TGTTGACCCC ATGTACCTGA GTGACCCCCA CGTACCTGAG TGTGACAAGC ACTATGGTGC 780
TTGACCTCAG TCCAGCTGCT TAGACCTGTA CCTGCCACAG CCCCACGTGC TGACACCTTG 840
CGTCTTGAGT TTTGATAAAT CTATCCTTTG GCTGATTAAT ATGACTGAGT GGTGTCTTCT 900
GACCCCATTT CTTATCTGGA ACACTGTGTC CTGACTTCAT TTCCTGTCTG GAGCACACTG 960
TCCTGACCTC ATTTCCTGTC TGGAACACAC TGTGTCCTGA CCTCATTTCC TGCCTGGAGC 1020
TCTCTGTGTC CTGACCTCAT TTCCTGTCTG TGCCGCTCTG TCCTGACCTC ATTTTCTGTC 1080
TGTGCCACCC TTTGTCCTGA CCTCATTTCC TGTCTGGAAC ATGCTGTGTC CTAACTGCAT 1140
TTCCTGTCTG GAGCTCTCTC TGTCCTGACC TCATTTCCTG TCTGGATCTC TCTATGTCCT 1200
GACCTCATTT CCTGTCTGGA ACATGCTGTA TCCTGATATC ATTTCCTGTC TGTGCCACTT 1260
TGTCCGGACC TCATTTTCTG TCTGGAGCAC TCTGTATCCT GACCTCATTT CCTGTTTGTG 1320
CCACCCTTTG TCCTGACCTC ATTTCCTGTC TGGAACATGC TGTGTCCGGA TTGCATTTCC 1380
TCTCTGGAGC TCTCTCTGTC CTGACCTCAT TTCCTGTCTG GAGCCAGTGA CCTCATTTCC 1440
TGTCTGTGTC ACTCTGTCCT GACCTCATTT CCTGTCTGTG CCACTCTTTG TCCTGACCTC 1500
ATTTCCTGTA TGCAACACAC TGTGCCCGGA CTGCATTTCC TGTCTGGAGC TCTCTCTGTC 1560
CTGATCTCAT TTCCTGTCAG GAGCACTCTG TGTACTGACC TCATTTCCTG TCTGTGCCAC 1620
TCTTGTGTCC TGACCTCTTT TCCAGTCTGT GCCACTCTGT GTCCTGACCT CATTTCTTAT 1680
CTGTGCCACT CTGTGTCCTG ACCTCATTTC CTGTCTGGAG CACTCTGTCC TGACCTCATT 1740
TCCTGTCTTG TGTCCTGACC TCATTTCCTG TCTGGAGCTC TCTGTGTCCT TACCTCATTT 1800
CCTGTCTGTG CTGCTTTCTG TCTTGGAGTT GCGTGCCTGA CCTCATTTCC TCTCCACTGT 1860
GTGTTCCTGG AGTTAGGCAT CATCTTGGTT TTTACTCCCT TGCTTGGTTT TCTCAGGATC 1920
TCTGGCTGCT CCGTCCTTGC TCCAGCGTTC TTCTCTGCCC CCTCCCTCTG TGGTCCAGAG 1980
GCCGATGGCC AGCTGGCCCT CACCTGCCCG CCCTGGGTAT TTCTGTGCTC TTCCTGGTGA 2040
GGGATTCTAG GGGTTCCCCT CCTGGGTTCA TCCTTACCTG AGTAGCCACA GCACACTGTG 2100
CAGTTGGGTG CCTGGGAGGC ACGTGCTTTG GGTGTTGCAT GGCTGACCTG GTAACTGGGC 2160
ACCCGTGTAT GGAGGGCTGG AACAGAACAC TTGTCGGCGC TCCTCAGCGT CTTGCCTCTG 2220
GTGTCCCCAT GGCGAAGTCC CCTGCCATCT GCTTTGGGCT CTGACATGTG ACCTGACTGT 2280
GCCCTTCAGG AGCTTTCAGA ACCTCCTCTT AGATCTGGCA TTCAAAATGT CTTGTCAGAC 2340
ACCTCGAGGC GGCTTGTGTT TGGCCCTGTG TTGGGCGCCT ATTGGGCCCT TGTCAGGTTT 2400
TTGTTGCCAG GAGGCTCGCG CCCCGATCTT CGGGATGGTG CCCGTGGCAT CTTCTGCTCG 2460
GTGCTCCCTA GGGCTGGACG TTGGTCCTCC TGGCACTGGT GCTCCGGTTG CTGTGGTCTC 2520
CCTGCTGTTC CCTTGTGGCT CAGGATTACT CTCTGGAGGT CTCCGCCTTA TCATGAGCAC 2580
TTTCTTTGTT GGCTACTTTT AGTTTCATGA TTTCATTTTC GTTTCTAAGA TATCTATCTC 2640
TTTGTAAAAG CTCCCACCTT TTGTGACTTG TGGATGCTGT ATCTTTCTCC TGTTGCTGCA 2700
GACATTAATG ATGTTTTTCT TGACAGTTTG TCCTGCTGGT TTCCTCTGCA TTCCTTTGGT 2760
TGGTTTCAGA CCTCGGCTTT AAAGGGGCAT TTCCCCACAT TGCCAATTCT TGACCATCTG 2820
GTCACGTCAA GGCTGACGTG CCAATGGCTG CAAGGGGGAG GGCACCTGGG AGCCCGCGGA 2880
TGGCTCTTAT GCAGACGTGC GGGCCAGCCC CGATCCTGCT TCTGCAAGGC CTCCCCTCCC 2940
ATGGTGGCGC TTTGGTGCCA GAGCGCGTCG GCGTGGCTCC CTAGCGTCTG CCTCTGCAGC 3000
TGCTTGGCCC CCAGCCGCCT CCTCCCAGCT GCCTCCTGCC CTATGTGTGC TTGAGCTCGA 3060
GACAATGCTT CCTTCATCCA AGAGCCGGGC TCTCGGCGAT TTTTGAGAGG AGAATGGGGT 3120
TGAAGCGATG 3130