EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-07234 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr12:47599310-47602200 
TF binding sites/motifs
Number: 26             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EGR3MA0732.1chr12:47600525-47600540CCCCGCCCCCGCAAC+6.3
EWSR1-FLI1MA0149.1chr12:47599537-47599555GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr12:47599545-47599563GGAAGGAAGGAAAAAAAA+6.18
EWSR1-FLI1MA0149.1chr12:47599529-47599547GAGAGAGAGGAAGGAAGG+6.25
EWSR1-FLI1MA0149.1chr12:47601374-47601392CAGACCTCCCTTCCTTCC-6.25
EWSR1-FLI1MA0149.1chr12:47599533-47599551GAGAGGAAGGAAGGAAGG+8.32
EWSR1-FLI1MA0149.1chr12:47599541-47599559GGAAGGAAGGAAGGAAAA+9.07
Foxd3MA0041.1chr12:47602024-47602036GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr12:47602028-47602040GTTTGTTTGTTT+6.32
GATA2MA0036.3chr12:47601132-47601143ACAGATAAGAA-6.14
Gata1MA0035.3chr12:47601132-47601143ACAGATAAGAA-6.62
HEY2MA0649.1chr12:47601947-47601957GACACGTGCC+6.02
IRF1MA0050.2chr12:47600575-47600596ATGTTAAAAATGAAAGTGAAG-6.18
IRF1MA0050.2chr12:47600388-47600409GTCTTTTTTCAGTTTCTCTTT+6.34
MYCMA0147.3chr12:47601307-47601319GGGCACGTGGGC-6.44
Npas2MA0626.1chr12:47601947-47601957GACACGTGCC-6.02
TFAP2AMA0003.3chr12:47601221-47601232TGCCTGAGGCT-6.32
ZNF263MA0528.1chr12:47599523-47599544GAGGGAGAGAGAGAGGAAGGA+6.22
ZNF263MA0528.1chr12:47599502-47599523GGAGAAGAGGAGGGAGGAAAA+6.28
ZNF263MA0528.1chr12:47599514-47599535GGAGGAAAAGAGGGAGAGAGA+6.37
ZNF263MA0528.1chr12:47599538-47599559GAAGGAAGGAAGGAAGGAAAA+6.56
ZNF263MA0528.1chr12:47599534-47599555AGAGGAAGGAAGGAAGGAAGG+6.58
ZNF263MA0528.1chr12:47599499-47599520GAGGGAGAAGAGGAGGGAGGA+6.68
ZNF263MA0528.1chr12:47599495-47599516GAAAGAGGGAGAAGAGGAGGG+7.08
ZNF263MA0528.1chr12:47599507-47599528AGAGGAGGGAGGAAAAGAGGG+7.66
ZNF263MA0528.1chr12:47599511-47599532GAGGGAGGAAAAGAGGGAGAG+7
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_11678chr12:47595248-47615259CD20
SE_12426chr12:47599987-47602334CD3
SE_15130chr12:47599770-47603135CD4_Memory_Primary_7pool
SE_16515chr12:47600124-47603456CD4_Naive_Primary_8pool
SE_18471chr12:47598003-47620164CD4p_CD25-_Il17-_PMAstim_Th
SE_20636chr12:47598124-47604287CD56
SE_22240chr12:47600030-47613913CD8_Naive_8pool
SE_22759chr12:47598038-47605635CD8_primiary
SE_60920chr12:47587105-47622074DHL6
SE_62568chr12:47583867-47618703Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr124759972247599955
Number: 1             
IDChromosomeStartEnd
GH12I047204chr124759836147604566
Enhancer Sequence
CTATAAACTA AGTTCCTGCC AAAGTTAGTT CAGCCTATAC CCAGGAATGG TGTAACAGCT 60
TGGAAATTAG AAGCAAGGTG GAGTCAGTTA GGTCAGATTT CTTTCACTGA CATAATTTTC 120
TTAGTTGTAA TTTTTGCAAA GTCAGTTTCA ATAGGTTTTT ATGAATAGGA GGAAAGAAAG 180
AGAGGGAAAG AGGGAGAAGA GGAGGGAGGA AAAGAGGGAG AGAGAGAGGA AGGAAGGAAG 240
GAAGGAAAAA AAAGGGGCAA TAACCATGTA ACCGCCTAAG GGGTTCACCT TGCCCACTGC 300
GTAGACAGAG CCAATTCACC AAAATAAGGG AATTGGAATA GAGAAAGAGT AATTCACGCA 360
GAGCCAACTG TGCAGGAGAC CAGGGTTTTA TTATTACTCA AATCAGTCTC CCCCAGCGTT 420
TGGAGAGCAG AGTTTTTAAG GACAATTTGG TGGGTTGGGG GAAGCCAGTG AGCCAGGAGT 480
GCTGATTGGT TAGGGATGAA ATCACAAGGA GTCGAAGCTG TCTTCTTGCG CTGAGTCAGT 540
TCCTGGGTGG AGGGCACAAG ATCAGATGAA CCAGTTTACC GATCTGGATG GTGTCAGCTG 600
ATCCATCACA TGCAGGGTCT GCAAAATATC TCAAGCATTG ATCTTGGGAG CAGTTTAGGG 660
AGGGTCAGAA TCTTGGAGAC TCCAGCTGCA TGACTCCTAT CCATAATTTC TAATCTTGTG 720
GCTCATGTTA GTCCTACAAA GGCCATCTAG TCCCCAGACA AGAAGGAGGT CTGCTTTGGC 780
AAAGGGCTGT TATCATCTTT GTTTCAAACT ATAAACTAAA TTTCTCCCAA AGTTAGTTCA 840
GCCTATGCCC AGGAATGAAC AAGGACAGCT TGGAGGTTAG AGGCAAGATA GCTAGCGTTG 900
GTTAAGTTAG ATCTCTTTCA CCGTCTCAGT CATAATTTTG CAAAGGCAGT TTCAACCATA 960
GTCAGCCCTC AGTAAGTACT AACCATAATA TTGTCAATGA TTGGCACCAG GCTTGGTGTG 1020
TTTTGCTCCA CCTCCTGCCT CCTTGGTAAT TCCTCAGCCT GCTGGGGACA AGGCAAAAGT 1080
CTTTTTTCAG TTTCTCTTTA TATGAATTGA TCATTTTTCA ACTGCTAGGT TTTCTTTGGG 1140
GGACTGAGGC AGAAGGATCA CTTGAGGCCA GGAGTTCAAG ACCAGCCTGG TCAATATAGC 1200
GAAACCTCAT CTCTACCCCG CCCCCGCAAC AAAAAAAAAA TCCAAGGTTT TTTTAAGGAC 1260
CTTGTATGTT AAAAATGAAA GTGAAGAAGT AGATCTGACG GTAGTTACAG ACACTACCCT 1320
GTTTCTACCT TCCACTCTGT GCTCTCAAAT CCCAACATCA CCAACATAAA TAAATGGTGA 1380
TTAGATGCTT TAGCCAGCAT TTGCTCTTGC CTTAGGTAAA TGGCTATTCG AATGGCCAGG 1440
GACTTTGACA TACTCATCCA ACTGAAGCTG AACTCAACTT GGCAGGCTCT GCCCAGGTAG 1500
AAGGAGCTTT GAATGGGATT TTAGCAAACA ATCAGATGTT ACCAAAATCT TATTAGGAGA 1560
ACAGCATGTA GAGTTACCCT GTGGTCTCTA GCTCAGGGCC TTGAGGGAAT ATCCTTTCAG 1620
AGCCTAGATG GAGCCCCATG GTCAATGCAC CAAGAAAATA AAGGACTTTA GCCTGAAGGT 1680
GACAGATGGA GGACTAAATT ACTTTAAACT TTTGTCCAAA ATACATAAAC ATATTGCTAG 1740
AATAATATCA GTGTTGGTTT GAATAGCCTG TTGGATTGGT TGAGATGAAG TAAGGAGCTG 1800
GCAGCTGGGC TCATCTGGTA GCACAGATAA GAACCTAATT AGCTCTATGA AAGAGGAAGC 1860
CCTGTGCCAC CTCCCCAGAG CTGTGTGAGG CCCAGGGGCA CACCTTCCAG CTGCCTGAGG 1920
CTGCTGCCTC CTCCCAGTCC CACTGAGGAA AGGAAGTGCT CTTTCTCTCC TGATAGGACA 1980
AGGATGACCC AGCAGATGGG CACGTGGGCA GGCAGAGCTC TCAACTACCT TTTCTCTTAG 2040
CATGGGTGAC AGTGTGTATG ACCACAGACC TCCCTTCCTT CCTCTTTGCT TTTATGGACC 2100
AAGCGATGGA AGGAAATGAC AATAAGGAAA TCTTCCTTAC ACAAATATGT AAGTATGCAT 2160
TCCTCTTCAT CAGACACAAT CACAACTTAA AGAACTTGCA TCAGTCTTGT GAGCTGGCCC 2220
CTAACCCCTG ACTATAATCT ATTATTCTTA AGATACCTAC TGAGAGAACT TATTCAGATA 2280
AAACATTTTA GGGCTTTTTG GAGCTTTTCT ATTTAAAGAA TAACAAGCTC CTTCTCTAGT 2340
TTTCTTTAAC AAACTAAGCA TATGACAGGC AGAGGTTACA GATTTTTCAT AGCTTACTTC 2400
CTCCTGAAAT TTAAGTCTGT GGTTAATCAA GCTCTGTGAA TGACAGTTTC TCCCTCGAAC 2460
TTTGTGGGCT AACACAGCTC TCTGAACACC CATAATTTGT TGGGTTTTTT TTTTCTTTTT 2520
TTCCTGAGCA GTGTAAACAA TTGTAAAGCT TTAAATAAAT AAGCTATAAG AAGTTTTCCC 2580
AGGGTCTTGA TTCTGTGACT CCACCAGGTG TCAAGGTCTC TGAACCGGCT GCCCTTAGAC 2640
ACGTGCCTGA ACTCAAAGCA GTCATACTGT TAAGGGATAG ACTTGGTGCT GTAAACTTAG 2700
CCATTTTGGT TTTTGTTTGT TTGTTTGTTT TCAGACAGGG TCTCATCTCC CAGGCTGGAG 2760
TGCAGTGGCA CGATCATAGC TCACTGCAGA CTTGACTTTC TGGGCTCAGG TGATCCTCCC 2820
ACCTCAGCCT CCTGAGTAGC TGAGTATAGC ACGCACCACC ACCCTCAGCT AATTTTTTAT 2880
TTTTATTTTT 2890