EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS190-02894 
Organism
Homo sapiens 
Tissue/cell
Treg_cell 
Coordinate
chr12:47599460-47602200 
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
ATAGGTTTTT ATGAATAGGA GGAAAGAAAG AGAGGGAAAG AGGGAGAAGA GGAGGGAGGA 60
AAAGAGGGAG AGAGAGAGGA AGGAAGGAAG GAAGGAAAAA AAAGGGGCAA TAACCATGTA 120
ACCGCCTAAG GGGTTCACCT TGCCCACTGC GTAGACAGAG CCAATTCACC AAAATAAGGG 180
AATTGGAATA GAGAAAGAGT AATTCACGCA GAGCCAACTG TGCAGGAGAC CAGGGTTTTA 240
TTATTACTCA AATCAGTCTC CCCCAGCGTT TGGAGAGCAG AGTTTTTAAG GACAATTTGG 300
TGGGTTGGGG GAAGCCAGTG AGCCAGGAGT GCTGATTGGT TAGGGATGAA ATCACAAGGA 360
GTCGAAGCTG TCTTCTTGCG CTGAGTCAGT TCCTGGGTGG AGGGCACAAG ATCAGATGAA 420
CCAGTTTACC GATCTGGATG GTGTCAGCTG ATCCATCACA TGCAGGGTCT GCAAAATATC 480
TCAAGCATTG ATCTTGGGAG CAGTTTAGGG AGGGTCAGAA TCTTGGAGAC TCCAGCTGCA 540
TGACTCCTAT CCATAATTTC TAATCTTGTG GCTCATGTTA GTCCTACAAA GGCCATCTAG 600
TCCCCAGACA AGAAGGAGGT CTGCTTTGGC AAAGGGCTGT TATCATCTTT GTTTCAAACT 660
ATAAACTAAA TTTCTCCCAA AGTTAGTTCA GCCTATGCCC AGGAATGAAC AAGGACAGCT 720
TGGAGGTTAG AGGCAAGATA GCTAGCGTTG GTTAAGTTAG ATCTCTTTCA CCGTCTCAGT 780
CATAATTTTG CAAAGGCAGT TTCAACCATA GTCAGCCCTC AGTAAGTACT AACCATAATA 840
TTGTCAATGA TTGGCACCAG GCTTGGTGTG TTTTGCTCCA CCTCCTGCCT CCTTGGTAAT 900
TCCTCAGCCT GCTGGGGACA AGGCAAAAGT CTTTTTTCAG TTTCTCTTTA TATGAATTGA 960
TCATTTTTCA ACTGCTAGGT TTTCTTTGGG GGACTGAGGC AGAAGGATCA CTTGAGGCCA 1020
GGAGTTCAAG ACCAGCCTGG TCAATATAGC GAAACCTCAT CTCTACCCCG CCCCCGCAAC 1080
AAAAAAAAAA TCCAAGGTTT TTTTAAGGAC CTTGTATGTT AAAAATGAAA GTGAAGAAGT 1140
AGATCTGACG GTAGTTACAG ACACTACCCT GTTTCTACCT TCCACTCTGT GCTCTCAAAT 1200
CCCAACATCA CCAACATAAA TAAATGGTGA TTAGATGCTT TAGCCAGCAT TTGCTCTTGC 1260
CTTAGGTAAA TGGCTATTCG AATGGCCAGG GACTTTGACA TACTCATCCA ACTGAAGCTG 1320
AACTCAACTT GGCAGGCTCT GCCCAGGTAG AAGGAGCTTT GAATGGGATT TTAGCAAACA 1380
ATCAGATGTT ACCAAAATCT TATTAGGAGA ACAGCATGTA GAGTTACCCT GTGGTCTCTA 1440
GCTCAGGGCC TTGAGGGAAT ATCCTTTCAG AGCCTAGATG GAGCCCCATG GTCAATGCAC 1500
CAAGAAAATA AAGGACTTTA GCCTGAAGGT GACAGATGGA GGACTAAATT ACTTTAAACT 1560
TTTGTCCAAA ATACATAAAC ATATTGCTAG AATAATATCA GTGTTGGTTT GAATAGCCTG 1620
TTGGATTGGT TGAGATGAAG TAAGGAGCTG GCAGCTGGGC TCATCTGGTA GCACAGATAA 1680
GAACCTAATT AGCTCTATGA AAGAGGAAGC CCTGTGCCAC CTCCCCAGAG CTGTGTGAGG 1740
CCCAGGGGCA CACCTTCCAG CTGCCTGAGG CTGCTGCCTC CTCCCAGTCC CACTGAGGAA 1800
AGGAAGTGCT CTTTCTCTCC TGATAGGACA AGGATGACCC AGCAGATGGG CACGTGGGCA 1860
GGCAGAGCTC TCAACTACCT TTTCTCTTAG CATGGGTGAC AGTGTGTATG ACCACAGACC 1920
TCCCTTCCTT CCTCTTTGCT TTTATGGACC AAGCGATGGA AGGAAATGAC AATAAGGAAA 1980
TCTTCCTTAC ACAAATATGT AAGTATGCAT TCCTCTTCAT CAGACACAAT CACAACTTAA 2040
AGAACTTGCA TCAGTCTTGT GAGCTGGCCC CTAACCCCTG ACTATAATCT ATTATTCTTA 2100
AGATACCTAC TGAGAGAACT TATTCAGATA AAACATTTTA GGGCTTTTTG GAGCTTTTCT 2160
ATTTAAAGAA TAACAAGCTC CTTCTCTAGT TTTCTTTAAC AAACTAAGCA TATGACAGGC 2220
AGAGGTTACA GATTTTTCAT AGCTTACTTC CTCCTGAAAT TTAAGTCTGT GGTTAATCAA 2280
GCTCTGTGAA TGACAGTTTC TCCCTCGAAC TTTGTGGGCT AACACAGCTC TCTGAACACC 2340
CATAATTTGT TGGGTTTTTT TTTTCTTTTT TTCCTGAGCA GTGTAAACAA TTGTAAAGCT 2400
TTAAATAAAT AAGCTATAAG AAGTTTTCCC AGGGTCTTGA TTCTGTGACT CCACCAGGTG 2460
TCAAGGTCTC TGAACCGGCT GCCCTTAGAC ACGTGCCTGA ACTCAAAGCA GTCATACTGT 2520
TAAGGGATAG ACTTGGTGCT GTAAACTTAG CCATTTTGGT TTTTGTTTGT TTGTTTGTTT 2580
TCAGACAGGG TCTCATCTCC CAGGCTGGAG TGCAGTGGCA CGATCATAGC TCACTGCAGA 2640
CTTGACTTTC TGGGCTCAGG TGATCCTCCC ACCTCAGCCT CCTGAGTAGC TGAGTATAGC 2700
ACGCACCACC ACCCTCAGCT AATTTTTTAT TTTTATTTTT 2740