EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS157-02320 
Organism
Homo sapiens 
Tissue/cell
PANC-1 
Coordinate
chr11:1356040-1358900 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs199527622chr111357872hg19
TF binding sites/motifs
Number: 33             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr11:1356350-1356367TGATTTTGAGGAATTCA+6.1
KLF16MA0741.1chr11:1357943-1357954GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1357965-1357976GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1357986-1357997GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1358006-1358017GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1358025-1358036GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1358038-1358049GGGGGCGGGGC-6.02
KLF16MA0741.1chr11:1358060-1358071GGGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357922-1357932GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357927-1357937GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357944-1357954GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357966-1357976GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1357987-1357997GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1358007-1358017GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1358026-1358036GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1358039-1358049GGGGCGGGGC-6.02
KLF5MA0599.1chr11:1358061-1358071GGGGCGGGGC-6.02
SP2MA0516.2chr11:1357984-1358001CGGGGGGCGGGGCGTGG-6.27
SP2MA0516.2chr11:1358036-1358053GTGGGGGCGGGGCGTGG-6.32
SP2MA0516.2chr11:1357941-1357958GGGGGGGCGGGGCGTGG-6.63
SP2MA0516.2chr11:1357963-1357980GGGGGGGCGGGGCGTGG-6.63
SP2MA0516.2chr11:1358058-1358075GGGGGGGCGGGGCGTGG-6.63
SP3MA0746.2chr11:1357942-1357955GGGGGGCGGGGCG-6.11
SP3MA0746.2chr11:1357964-1357977GGGGGGCGGGGCG-6.11
SP3MA0746.2chr11:1357985-1357998GGGGGGCGGGGCG-6.11
SP3MA0746.2chr11:1358059-1358072GGGGGGCGGGGCG-6.11
ZNF263MA0528.1chr11:1357320-1357341AAAGGAGTGGGGTGGGGAGGG+6.08
ZNF263MA0528.1chr11:1357590-1357611CTCCTCCCTCCTCCCACCTCC-6.19
ZNF263MA0528.1chr11:1357560-1357581CCTCCCCCCTCCCCCGCCCTC-6.3
ZNF263MA0528.1chr11:1357547-1357568CCTCCCCCGCCGTCCTCCCCC-6.45
ZNF263MA0528.1chr11:1357579-1357600TCTCTCCCACCCTCCTCCCTC-6.67
ZNF263MA0528.1chr11:1357583-1357604TCCCACCCTCCTCCCTCCTCC-7.51
ZNF263MA0528.1chr11:1357576-1357597CCCTCTCTCCCACCCTCCTCC-8.03
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1113581051358800
chr1113566001357964
chr1113578631358286
Number: 1             
IDChromosomeStartEnd
GH11I001335chr1113564721359269
Enhancer Sequence
TAGTAGAGAC AGGGTTTCAC CGTGTTAGCC AGGATGGTCT CGATCTCCTG ACCTCATGAT 60
TCGCCCGCCT CAGCCTCCCA AAGTGCTGGG ATTGCAGGCG TGAGCCGCTG CGCCTGGCCC 120
CTTTGCCATT TTTTAATTGA GCTGCTTGTC TTTTCGTTGT CAAGTTGCAA TTGTTCTTTG 180
TGTAATATAA CCCCCTTTAT ATATGCCAGA TACAAGTCTC TTATAGACAA GTGATTTGCA 240
AATATGTTCT CCCATTTTGC AGATTGTTTT TTGGTTTTCT TGATGGTGTC CTTTGAAGCA 300
CAAAATTTGT TGATTTTGAG GAATTCAGTT TATCTATCTT TTTCTTTTGT TTCTGTGCTT 360
TTTGGGTCAT ATCTAAGTAA ACCAAGCTCA AAAAGATTCA CCCCATGTCT TCTCAGTGAT 420
TTATAGTTTG AATTTCTACA TCTAGGTCTT TAACCCACTT TAAACTAATT GTTCTATGTG 480
GTATGAGGCA CCTGTCTCTT CCTAGAGACC ACTGCACTCC ACCTGTCCCT GAGAATGACT 540
CCTGACTCCA CTGCATACGA GTCCCTCTCC CCCACCTTCT ACCTGGAAAA CTCCTATTCA 600
TCCCATCAAG ACCCAGCCCT GGGTTGCTCC TGGGTGGCTT TTTTCACTCT CCTTGGCAGC 660
TTTAACTGCT GCCTGGGATG TGGGCTCAGG GCCAGTGCCC TGGAGGGCCC CTGTCATAGC 720
CCTTCTCACC AGCACTGAGA TTGGTCACCT CCGAGTCTGG TGGGCCCGGG GCCCCCATGC 780
AGGTGCACAC AAGTGCTGCT GAGTGACTGG TGATCATACA GCCAACATTC GCGGTGACAT 840
TCATGCACCG GGGACTTCAC AATTCCCCGG ACTCGTCATA AGGGCTGCTC GGCCCCATCT 900
TACAAATGGG GAAACTGAGC CTGGGGGGTT CAGTAACTTG CTGAGTTCAC ACAAACAGTG 960
AGTGGATGGC TGGATGAGTT TGTAAAAGGA AGGTCGATTC TGCATGATGA AGCTAAATTG 1020
GAGCCCAAAA TTCTCTCTTC CGGCCCCCAG TAGAATATTA TGGGTGCACC CAAAGGAATG 1080
TAAAAAGACC AGATGCCCAG GACACGGGGC GGTGCCTGAT GAAACAGCTG CATTAGAGAG 1140
TGACTTTGCA ACTCTGGAGA GAAGCCACTG AAACCCAGCG CTCCTATAAA TAGCAGCTCT 1200
TGCAAAGCAT CGGGTGTGAA TTTTCGTGGT GTTGGCAAAT TCAGAGATTG AGAAATCCAG 1260
AGACGTTCAT GTTCCCGGAG AAAGGAGTGG GGTGGGGAGG GAGGTCGCAA GCAATGCCAT 1320
CTTCAGGAAC AAAACTCCTG CATAACGAAG CCCAGGTTTC TGTGTTTTCG TGGGTGTTCC 1380
CGGGCACCTT CGGGCAGGTG GCCCCAGGCG ATGTTGTGTG TCTCTCCTGG CTGTGGACGA 1440
ATGGACGCCT GGGGTGAGGC TGGGCCAGGG ACCTGGGGCT TGTGGGTGTC GGCTCCCATC 1500
CCGGGGTCCT CCCCCGCCGT CCTCCCCCCT CCCCCGCCCT CTCTCCCACC CTCCTCCCTC 1560
CTCCCACCTC CCCTGCCCTC TCCCACCGGC GTGCACCCCC CCGCCCCGCT GCTCACCGCC 1620
CACCACTCCC CAGAGGCCGC TTGCTTCCCC GTCTTTGGCC CTGGGCCCCC AGTACCGCCC 1680
CGTGCCCCCC TCACTTCTCC CCCGGAAGCG CATCCGTCAG GGAAACCGTC CTAAGACCGT 1740
CCGCACTCGC TTCAGAGCCG CTGCAAACGG CCGTCAATCC GTCATTCAGA CGCGAAGACA 1800
AAGCGTCCCT GGCTCAGCCC TGAGAAGCAG CGGGACGGCG GCGCGTTCCT GAGTTCCCGC 1860
CACGCGGGCG CCCGGCGAGG GCGGGGCGGG GCGGGGCGGG CGGGGGGGCG GGGCGTGGAG 1920
GGCGGGGGGG CGGGGCGTGG AGGGCGGGGG GCGGGGCGTG GAGGGCGGGG GCGGGGCGTG 1980
GGGGCGGGGG CGGGGCGTGG GGGCGGGGCG TGGAGGGCGG GGGGGCGGGG CGTGGAGGGC 2040
GGGGGGCGGG GGGATGGGGA CAAGGTAGGG GTCGTGGGGC GCTGGGCTCA CCCCAGGCCC 2100
TCAGGTGTCT CGAGATGGCC CGGGCTCCGA GCGCTCCCGG CGCTTACGCT AGAGCCTCCT 2160
CCTGTGCGAA ACGCGTCCGT GCCCAGGCGC GGGGACCCTG CAGGGCTGTG GGTTCGCGCT 2220
GCCGCTGATC CTGCGTCTTC CCCCCTCCCA GGCCCCGCGT CCAGCCCGCC CCGCCCGCGG 2280
TGGGAGACGC GCCCTCCAGG TGCGGATGAG ACGCGCGGAC AGCGGGATGG AGAAGGTGAG 2340
ACCTGTCCGG CCCCCGCCTC GCGCTCCCGC TTCTCCAGGA AGAGGTGTCG CCGCCGCCCG 2400
GGGGTCCCCG TCCCTCCCTA GCCCGATCCC CCGGAGCCGC GGCCCCACCA CCGCCTGGCA 2460
CTCCCGGGAG CGCGCGGCCT CGGAGCCCCC AGCCCCGCAC AGCCCCTTGT CCCCGGCTGG 2520
GAATGGCGCC TCGCACGGGG TCCCTCGGAG GCCGCGAGGC TCCGCTCGGC GTGTTCGGAA 2580
GCCACCCCCA GCTCCCCCGG CAGCTTGGAG CCTCAGAAAC GCGGGGCAGA GACGCGACAC 2640
GGAGCCGCCT GGCACTGAGA CTCCCCAGTG GCTGCGCCGC CTTCCCGGGG GCCCGAGGCG 2700
GGGGCGGGGG GCGCGCTCGC TTCTTCCCCT CGCGGGGGTC TTCCCAGCCC ACCGGCCACG 2760
GCCGCTCCGT TCCAAGCGCG CTTTTCATTC CGCGTCATCT TATCTGACAA ACGTTAAAAA 2820
GAGGGAGGGT GGGAGGCCCC GAAGTCCCAC CCGAGTCCCC 2860