EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-00057 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr1:3267890-3270340 
TF binding sites/motifs
Number: 25             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr1:3268739-3268750GCAGGGTGTGG-6.62
RREB1MA0073.1chr1:3270260-3270280AGGCTGGTGGAGGTTTGGGG-6.03
RREB1MA0073.1chr1:3269356-3269376CCCCAACTCATCCCCCTCCC+6.18
ZNF263MA0528.1chr1:3268282-3268303CCCTCCCTCTGTCTCTCCTCT-6.05
ZNF263MA0528.1chr1:3268101-3268122CCCTCTCTGTCCCCCTCCCTC-6.16
ZNF263MA0528.1chr1:3268189-3268210CCCCCTCCCTCTCTCTCCATC-6.17
ZNF263MA0528.1chr1:3268124-3268145TCATCCCCTTCCTCCTTCTCT-6.18
ZNF263MA0528.1chr1:3268295-3268316TCTCCTCTCCCTCTCTCCCCC-6.39
ZNF263MA0528.1chr1:3268212-3268233TCTCTCTCCCCTCCCTCTTTC-6.44
ZNF263MA0528.1chr1:3268218-3268239TCCCCTCCCTCTTTCTCCCCT-6.48
ZNF263MA0528.1chr1:3268223-3268244TCCCTCTTTCTCCCCTCCCTC-6.54
ZNF263MA0528.1chr1:3268227-3268248TCTTTCTCCCCTCCCTCTTTC-6.61
ZNF263MA0528.1chr1:3268208-3268229TCTCTCTCTCTCCCCTCCCTC-6.67
ZNF263MA0528.1chr1:3268173-3268194CTCCCCCTCCCTCTCTCCCCC-6.6
ZNF263MA0528.1chr1:3268215-3268236CTCTCCCCTCCCTCTTTCTCC-6.6
ZNF263MA0528.1chr1:3268238-3268259TCCCTCTTTCTCTCCTCCCTC-6.74
ZNF263MA0528.1chr1:3268118-3268139CCTCTCTCATCCCCTTCCTCC-6.77
ZNF263MA0528.1chr1:3268270-3268291TCCTCTGTCTCCCCCTCCCTC-6.77
ZNF263MA0528.1chr1:3268179-3268200CTCCCTCTCTCCCCCTCCCTC-6.88
ZNF263MA0528.1chr1:3268149-3268170CCCTCTCTCTTCCCCTCCCTC-6.94
ZNF263MA0528.1chr1:3268159-3268180TCCCCTCCCTCTCTCTCCCCC-7.08
ZNF263MA0528.1chr1:3268235-3268256CCCTCCCTCTTTCTCTCCTCC-7.41
ZNF263MA0528.1chr1:3268165-3268186CCCTCTCTCTCCCCCTCCCTC-7.58
ZNF263MA0528.1chr1:3268121-3268142CTCTCATCCCCTTCCTCCTTC-8.3
ZNF263MA0528.1chr1:3268133-3268154TCCTCCTTCTCTCCCTCCCTC-8.42
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_01548chr1:3261400-3275654Aorta
SE_28099chr1:3268220-3269153Fetal_Intestine
SE_28099chr1:3269171-3273832Fetal_Intestine
SE_31959chr1:3268236-3270788Gastric
SE_40807chr1:3261779-3270921Left_Ventricle
SE_47515chr1:3267108-3268169Pancreas
SE_47515chr1:3268289-3270686Pancreas
SE_49549chr1:3262964-3268173Right_Ventricle
SE_49549chr1:3268208-3269152Right_Ventricle
SE_49549chr1:3269169-3270727Right_Ventricle
SE_65787chr1:3264747-3269292Pancreatic_islets
SE_65787chr1:3269308-3270534Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr132684243269000
Number: 1             
IDChromosomeStartEnd
GH01I003345chr132620933272904
Enhancer Sequence
TCCTGCTCTC CTGGGCTGGG TTTAGGGAAA AAGCTCCATC CAGGGCCCAC GTGGGGTCCC 60
AGAATTTCTT CAGAACCCAG AACCCGTCTC TATAGGAACG CAGAGGGAGC AGCACAGGGA 120
CATAGGTCTT CTCCTTCCCA TCCCTGGTCC TGGAGCAGGT GCCTGGGCCC TCAGCTCACT 180
GTGTCACATT GGAACCCGTC TCTGTCCCCC TCCCTCTCTG TCCCCCTCCC TCTCTCATCC 240
CCTTCCTCCT TCTCTCCCTC CCTCTCTCTT CCCCTCCCTC TCTCTCCCCC TCCCTCTCTC 300
CCCCTCCCTC TCTCTCCATC TCTCTCTCTC CCCTCCCTCT TTCTCCCCTC CCTCTTTCTC 360
TCCTCCCTCT GTCTCTCCCT TCCTCTGTCT CCCCCTCCCT CTGTCTCTCC TCTCCCTCTC 420
TCCCCCCCCT CTGTTTCTCT TCTTCCCTCC CTCTCTCTTG CTCTCTCTCA CCATAGCCCC 480
TCCTCTTGCA GTCTCCAGCC ATTTGGGGGG TTCCGCCTCC CCCTTGAGAA CTCACACACT 540
CACTCTGTGT CTGTGACTTG GTATGGAAGG GAGAGCTGGG GGCGGGGAGG CACTGATGCC 600
TGAGGGTAGC TGGGCTGTAC CATCCTCAGC CTCGCCCAGA CCCTCCAGAG ACCCTAAGGA 660
CCTCCCCAAA GAGCAAGATG ACCACACACT TTACCTCCAG AGGAGAGGAG ACACTCCTGC 720
GAGGGAATGG GGAGCACAGT GTGAATGACT CTGGGCAGCA TGACCAGCTC AGACAGCCCC 780
AGGCCAACCC TGGCACACCG GTGCATGGTC CACCTGCCTG GCACAGTCCA CCTGCCCGGC 840
CCTGGCACTG CAGGGTGTGG GCCCTTCTCC CTCCGTGTTT GGCCCTCTCT GCCATGGGCT 900
GGTGCTCCCC TCCACCCAGC CGTGCTGCCC CCACCTGCGG ACTGATTCAA TTCTGCCCCC 960
ATCCCAGCCG TGCCCACCCC TCCCACGACT TCCCACGGCA GAGTTGTGGT CCTGGCGGCT 1020
GGCTGCAGCT TTTAATTGTT TTTCTCCCCC CAGATGCTCT CCACTGACCC TCCCTCCCCT 1080
CCGAAGCCGG CGCCCCCCTT GCTGCCCGCA GTGGGCTGGG GGAGGGGACA CGGATTCCAG 1140
TAGCATTTCC GCCCTCCGCT CTATCATTTC GTTTGTTCTC CTTTCCTTTC CCTTTCTTCT 1200
CCCTCCACGG GCCCAGCCTC TGTGATTAAG CCTCAAGGCC TCCTGCTGCT TTTAATAGGC 1260
CTGCGGGCCT GACCATCTGA TGAGAACCGC GCAGCACAGC TTGTTCCCGA ATACTTGCGC 1320
TGGAATCGCC TAATGCACGG TATTAATCAT CACTGTCAGG CCGTTCAGGC CCTAAATACA 1380
CCCACCCAGT ATAAAATTAT CCTAAACAGA AAAGAAGCAG GCTGCGATTG GCCGCATATT 1440
GAAAACAGAC ATGAGACAGC CCCCGCCCCC AACTCATCCC CCTCCCAAAT TTCAGGGCCG 1500
CCTCCAAGGC CTCTGCCCGG TGTCAGGAAC AATAGCTAGC TCTCGGTGGC AGTCAGGCCG 1560
CATTTGGTGT TCACACAAGT CCCACGTCGG GGAGGGGGCC GTCCTCTGCA CAGGGCCCTG 1620
AGTGCCCACC CTGCAGGCTT CGGGGCCCAT GCGTGGCCGG AGGCAGAGGG CTTCCCGGTT 1680
GGGCTGAGGG CTGTTTCAGA GCAGTGCCCT GAGGAGGACC AGGCCTGGGG CTCTGGAGCC 1740
AGAAGTCAGG AAAGGGAGGC TGCAGCCGCA CACCCGAAGA GCTCGAAAGC TGGCCCCCAG 1800
CCCAGACTCC CACGCAGGGA CGTCCCTCAC AGCAGGATTT GCTGCTTCCT CCTGACCAAT 1860
GCCCTCCTGT AGTAAAAGTT AACCGGGTGT GAAATGCATG TTGCCTGAGG TGCGGTAAAA 1920
GTTTACGAGG GCTGGGCAGC TCCTAGGCAT GGGCAGGCCC ATTTCTCACC TGCAGCCTGG 1980
GTCCCTGCAG AAACCTGGCT CGGCCTGGGG GCTATGGCAG GGCCCTCATT GGGTGAGGGA 2040
GGCCCGGGGT ATTTCTTGCC ACATCTGAAA TTGGACCCGA ATGCGCATGG GGACACCATC 2100
CTGCAGCCTC TGCGTTTGTC CTTGGGGTCA TTGAGGAATC TCAGCACTGG CCCTGGCTTC 2160
TGGCAGGCAC CTGGGCCATG GGAGCCCAAG GGTGGCTCCC TCGGGCCACC CCGTTACACT 2220
CCAGCCAAGT ACTGGGGGCC ACGGGCTGAG GGCACAGGCC ACAGGGGATG AGTCCAGCCC 2280
CGCAGTGTGA CCGGCAGTTG GCAAACCATT GACTCAGGCC ACCTCACTGC ACCCACAGGC 2340
TTTGCAGAGA GAACAGGACA ATCCTAGCTC AGGCTGGTGG AGGTTTGGGG ATGCCGAAGC 2400
AGCCAGAGAG TGGCCAAGGG GGTTGCACTT GGGGCCGGAC CTCCTGACTC 2450