EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS182-19352 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr6:158439020-158443270 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NKX2-5MA0063.2chr6:158440290-158440300CTCAAGTGGT-6.02
Stat6MA0520.1chr6:158439876-158439891TTTTCTGTGGAAATG-6.18
TFAP2CMA0524.2chr6:158439040-158439052TGCCCGGGGGCA+6.02
TFAP2CMA0524.2chr6:158439040-158439052TGCCCGGGGGCA-6.37
Tcf12MA0521.1chr6:158439510-158439521CAGCAGCTGTT-6.32
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_01612chr6:158438628-158439647Aorta
SE_01612chr6:158439706-158441990Aorta
SE_02260chr6:158439101-158441015Astrocytes
SE_03167chr6:158438664-158441813Brain_Angular_Gyrus
SE_03167chr6:158442095-158442926Brain_Angular_Gyrus
SE_03982chr6:158438657-158440710Brain_Anterior_Caudate
SE_04807chr6:158428760-158450510Brain_Cingulate_Gyrus
SE_05791chr6:158414418-158455991Brain_Hippocampus_Middle
SE_06699chr6:158427905-158445004Brain_Hippocampus_Middle_150
SE_07755chr6:158429088-158446658Brain_Inferior_Temporal_Lobe
SE_19962chr6:158440537-158442456CD4p_CD25-_Il17p_PMAstim_Th17
SE_29930chr6:158438639-158443107Fetal_Muscle
SE_37125chr6:158437198-158441748HSMMtube
SE_37951chr6:158437235-158443186HUVEC
SE_38898chr6:158438580-158440957IMR90
SE_40902chr6:158438962-158441010Left_Ventricle
SE_42660chr6:158438993-158440820Lung
SE_44789chr6:158438849-158439696NHLF
SE_44789chr6:158439718-158440709NHLF
SE_45571chr6:158434391-158444034Osteoblasts
SE_47213chr6:158441954-158443221Panc1
SE_55691chr6:158438598-158440190u87
SE_55691chr6:158440234-158442083u87
SE_65268chr6:158437581-158439754Pancreatic_islets
SE_65268chr6:158439778-158441270Pancreatic_islets
SE_65268chr6:158442126-158445961Pancreatic_islets
SE_67484chr6:158438598-158440190u87
SE_67484chr6:158440234-158442083u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr6158440159158440546
Number: 1             
IDChromosomeStartEnd
GH06I158016chr6158437575158443335
Enhancer Sequence
AAGACAGGGA CCAGGGCAGA TGCCCGGGGG CACAGGGGTG GGCTGGGAGT TGTCAGCAGG 60
AGAAAAAAGC CACCGATGTG TGACTGTCAG TCAGTGTGGG GTGGGAGGGA GAGGAAGGGA 120
CAGTGTGATC TGACTTGCGA AGGGAGAGAA CTTCCAGGAA GACGTGGGCA TCTCTGCTCA 180
CTCTGAGAGA CTCGGGGGTG AGCCGGTGGT GGCCGGCTGT CGTGGGTGGT CACAGCCAAA 240
CTCAGCTGTT CCTGGAGCTC AGGAGCCCTG GGGCTTTAGG TTCTACCACC TGTTTCCTTC 300
CTTCTCTCTC AGGGGCCCCC TTGCCATCTG TGACCTGGCT GTGGACATCT CTTGTGACTT 360
CTGGGGCCGA GACAAGAGCC CAGTCGCATT CCTGATTCTC AGTCCCACCT GGCTGAGATG 420
GGAATGGCTG TATGGGTTGT CTGAATTCGG GCTTTCCCTG AGCCAAGCGC ACACCTCCCT 480
TCCCTGCTCA CAGCAGCTGT TTTCAGAGAC TGAGGATGTT TAAAGCTGCC AGAAAAGCAC 540
GGTTACGTTG GCCATTCCTT TTCTGGGTGT TTTCTGTCAT GGAATGTTTT TCCCTGAACT 600
GTGACGATTA CAGTGATCAT TTCCAAATAG CATTTAGGAA AAATACACAG TACCCACATG 660
ACAAAGTGCA TTTATGAAAT GTCTGTTTCG TGCCAAGAGC TAGCCGTACA TTCACTTATT 720
TAATCCTAAA AATAGGCTAC CGTGATAATG CATCTTTGTC CCCGTTTACA GTAACGGGAA 780
CAGGCTCAGA AGCTTCAAGT AACTTGCCTT AGGTCAGAAA CTTAGTTGGG GTTTGAAGCG 840
CCTCCAAACG CTTGCTTTTT CTGTGGAAAT GTGCGGGCTG CCGAGGGTTT TCTGCAGGAC 900
TTTCCGCTCT GCAGCGATCT TCCTGAAGTT GCAGGAAATC CCTGTGGCCC TTGCCTTCCA 960
TGGTGATGAC CGTGAGGATG GTGGCCTGCA CCTGCATGGG ACTCACTTAG GAACTTGTTA 1020
ACACGGCTCC CGAGGCCACC TGTGCTGTTG TCACCCTGCC TTGCAGGTGT GGCAGGGATG 1080
CCGCGTTCCA TCCATGCTGA TGCCCTTTTT TCCACATGGT AGTATCTGGG CCCCCAGGAT 1140
GCCTCACAGT CTTGGCTTCC TTCAGTTATA GTTGGCAGCT GCTTTTGGTC CTTACATGAA 1200
TGACTCATTT TGCATCCGAC AGGGACTGGG ATTCGACGAA TTACAGTAAC CGGCTCAAGG 1260
TCACGCCATT CTCAAGTGGT GCCCTGGGTT TTAAACTCAT GCCTTGCGGC ACCAGGGACT 1320
GCCTTCAACC ACCAGGCTGT TCTCCTTTCT GAAAGGGACA GGTGGCTGGG CTCACAAGGG 1380
GGACAGGAAG TGCAGTACCT TCCCCCATCC CAGGGGAAAA GTGTTTTTTC CCAGGGCTGT 1440
GATCTAAGAT CAGCTGTGGG AAATTGGTCC TAACCAGGAA GGGTGGCAGC CCCAAAGATG 1500
TCTTATTAGA GCGAGCCAGG GTGTCTGCGG GGGTCAGCAG GGTCTAATGG GGCAGGGAGT 1560
GCTCAGAGAG GAGACCACCT CCCAGGGCTG CCCTAGGCGA GGCCTCCTCC CTGCCTTCAG 1620
CCAGTCCCCG CCACCCCACA CCCCACAGAA GGGAATGAGG CTTCTTGTGG ACCATGCGAG 1680
ACCAGCCCTG CTCCGAGGCT TTGGGTGCCC CCAACCCCTG CCCACCTGTG AGAGTCACCC 1740
CCCGGAGTGG GTTGGAGTTT CTCTGAGTGT GGTGTGTATG AGTTTGACTT TGGCGATGTC 1800
AGGATAATTT GGTCTGTTTT CAACACATTC TGGAAAGCAC CCTGAGCATC TGAAGGATGG 1860
AAGGATTGGG CTTTAAATCA AGTTTTTTCA GTCCCCATTG GTTATCTTAA GGGGCGTTTG 1920
ACTTTAACTT GATTTTCTTT TTCCCCTGTA AGTCCCTGAC CCAGAACTGT GATCTATTTT 1980
CTTTTGTGTT TTCAGCTGTT GAGCATGTTG GGCAGCACGG AGTGTAGCTA CAACTGTGTG 2040
ACCCCACCTG TGTGACTGAC TCCACCTGTG TGACTCCAGT CGTGTGACCA ACTACAACTG 2100
TGTAACTGAC TCCAATTGTG TGACTAACTC CACCTGTGTG ACTCTGCGTG ACTCCAACTG 2160
TGACTCCATC TGTATGACTC CAATTGTGTG ACCCCCACCT GTGTGACTCT GACTGTGTGA 2220
CCCCCACCTG CGTGACTCTG ACTGTGTGAC CCCCACCTGC GTGACTCTGA CTGTGTGACC 2280
CCCACCTGCG TGACTCCGAC TGTGTGACCC CCACCTGTGT GACTCCAACT GTGGACTGAC 2340
TCTAACTATG TGACTGACTC CAACTGTGTG ACTAACTCCA CCTGTATGAC TCCAACTATA 2400
TGATTGACTT CAACCGTGTG ACCCCACCTG TGTGACTCCA ATTGTATGAC TGACTCTAAC 2460
TGTGTGACTC CAACTGTGAC TCCATCTGTA TGACTGACCT CAACTGTGTG ACCCCACCTG 2520
TGTGACTCCA ACTGTGTACT GACTCTGTGT GACTGACTCC ACCTGTATGA CTCCAACTAT 2580
ATGACTGACT TCAACCGTGT GACCCCACCT GTGTGACTCC AGTTGTGTGA CTGATTTCAC 2640
TGCGTGGCTA ACTCCACTGT TGCCTGACTC CAGCTGCGTG ACTTCAGCTG TGTGACTCCA 2700
TGTATGTGAC CCTAGCTGTG TGACTCCAAC TTTCAGTTGC CACGAAGACA ACCAGCTGAG 2760
TCAGGAGTGG GCCTCCCTTT CAATGTTTTT AGCTAAGCAT CTCTGCGCAA AGAAAGAGGC 2820
TTCCCCACAG GCTCTTAATT TGGGACAAGT TTTCCCTTAG TTTGGGAAAA ATTTCAATCT 2880
ACCTAAATTA GCCTTTTACA TTAGAAATCG AGAAATATGC ACAAAAATTC ATAAAAGCCT 2940
TTTTCCAGGT TCCAAGGTTT TTGTAGAAAG CCCAAAGTTC CCCTTTCCTT CCTGAAATGC 3000
CAGCAGGAAG GGGTTGGAGC TCCCGTGATT AGCCAGGGAG TCAGGCTTCC TGAAGTTTAC 3060
ACAATACAAA GCATATTAAG TGAGAATGTA GCAGAAAAAA GAACTTATCC CAATGATTAT 3120
AGCAATTTAA ATTCTCTTGA ACCCAAGCTC TCAAGGCCTA CCTGTTTTAT AGCCTCAAGG 3180
GACTCTACTC CTATCCCAGA CTATAATGAA TTGTGTCTCC TGGAGTTGTG CAGTACGCAA 3240
CCTGTGAAGC TGTACACGAC AGCCCTATAA ATTCTCTAGC AGACAGCCCT CCTAGATTCT 3300
AGTTCCCACT TCACAGCTGA ACTGCATTTA ATCTCTGTAG GACTGTTTTC CTGTCTGTAA 3360
ACCTGGGAAA ACTGCCTCAT CTCTATGTTG CCTAGTTCTC AGGAGGTCCA CATGGGCCAT 3420
GCACATGGTA GCCATGAAGA GTGTGGAGTG CTCCTCCAAC ACCAGGCGGG CTGGCCACAG 3480
GCAGTTTCTT AGAGTGTGGC CTGGGGACGC TGCCACCACT GAGAAGCTCT GCTGTCTCTC 3540
CTCTGTCCCT GGGAGGGCTG GAGGGAGGAG GGTGCTGAGT GAGAGGGACC TGGCCTGCAG 3600
AGGGCTGAGG ACGAGGTGTG AGCTGGAAGG CCAGGCTGTG TGGCCTCGGG GTGTGGACTC 3660
CTGGTGGGGG GCTCCTCTGC ACAGGCTAGC AGAGGGCTGG TTTCATGGGC AGTCACTTCA 3720
GAAGGAGGAT TCCCTGGAGG GGAGTTTGAA CCCTTAGTCT TTTGGGATGC AGTGTTCTCT 3780
AGCAAGTCTT GAAGCGAACT GGCCTTTGTC GGTCTTAGAT TAATTTAATT CCTGTGCCCA 3840
GTGGTGGGAT ATTACCAAGA GAGTTGACAC CCAGCTCCCT GAGGGGGAAG CTCTGAGATG 3900
ATGCAGCATT TGCCAGTTTC CAAGGTGTAA ATTCACGGGC CAGGGCTGAT TTCAGGTTCC 3960
CAGCGTGGAG CTGAGGAAGG ATCTGCACCA GGGGTGCTCA CTGCGGGTGT TCACTGCTGT 4020
GGCCGCCGCT GCCTACACCT CCCTCATGTT CTGCAGAAGG GAGGCGGGAG AAGGCCCTGA 4080
GACCATGCCG CATGGGCACA CAGTGCTTAG GGTTCTGAAC CTGCGGGTGG CGGGGGAGGC 4140
TCAAGGGTCA TCTGGCCGAA GCTTCCCCCT TCACAGGTGG GAAAGCCTAG ACATCTTTAG 4200
TCCTTTGTTT GGAGCTTTAA GTCTGAGGGT GTCTGTGTGA GCAGAGGGAC 4250