EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS141-17196 
Organism
Homo sapiens 
Tissue/cell
NB4 
Coordinate
chr7:75245800-75248190 
Target genes
Number: 13             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1186222chr775247329hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr7:75247611-75247621GGCACGTGCC+6.02
HES2MA0616.2chr7:75247611-75247621GGCACGTGCC-6.02
IRF1MA0050.2chr7:75247463-75247484TCTTTCTTTCATTTTTTTTCT+6.32
Nr2f6(var.2)MA0728.1chr7:75246615-75246630TGAACTCCTGACCTC-6.22
ZNF263MA0528.1chr7:75245935-75245956GGAGGAGGACGAGGAGGAGGA+10.26
ZNF263MA0528.1chr7:75245917-75245938GGAGGAGGAGGAGGAAGAGGA+10.86
ZNF263MA0528.1chr7:75245920-75245941GGAGGAGGAGGAAGAGGAGGA+11.13
ZNF263MA0528.1chr7:75245914-75245935GGAGGAGGAGGAGGAGGAAGA+11.36
ZNF263MA0528.1chr7:75245923-75245944GGAGGAGGAAGAGGAGGAGGA+11.79
ZNF263MA0528.1chr7:75245902-75245923GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr7:75245905-75245926GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr7:75245908-75245929GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr7:75245911-75245932GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr7:75245926-75245947GGAGGAAGAGGAGGAGGACGA+7.25
ZNF263MA0528.1chr7:75245932-75245953AGAGGAGGAGGACGAGGAGGA+8.11
ZNF263MA0528.1chr7:75245899-75245920TGGGGAGGAGGAGGAGGAGGA+8.68
ZNF263MA0528.1chr7:75245938-75245959GGAGGACGAGGAGGAGGAAGA+8.87
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_04465chr7:75246867-75247567Brain_Anterior_Caudate
SE_05143chr7:75246542-75247650Brain_Cingulate_Gyrus
SE_06030chr7:75246418-75249003Brain_Hippocampus_Middle
SE_07279chr7:75246613-75247686Brain_Hippocampus_Middle_150
SE_54400chr7:75245704-75246196Spleen
SE_54400chr7:75246223-75248730Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr77524720075248011
chr77524702475247489
Number: 1             
IDChromosomeStartEnd
GH07I075616chr77524588975248318
Enhancer Sequence
GGCTGGTCTT GAGCTCCTGG CTTCTAGCGA TCCTCCCACC TTAGCCTCCC AAAGTGCTGG 60
AATTACCGGC GCTAGCCACC ATGCCTGGCT TTTTAAGGGT GGGGAGGAGG AGGAGGAGGA 120
GGAGGAGGAG GAAGAGGAGG AGGACGAGGA GGAGGAAGAA ATAGTAGCAG CAGGAAGCCA 180
CAAAGCCAAA AACATTTACC ATCTGGCCCT TTGCAGAAAA TGTTTGCTGG CCCCTGGACT 240
AGGCAGGGCA GCCTATGAGG GTGGATGTCC ACACATACAG AGGCTGATTA CTGGCCATCA 300
CTTTGGGGTA AGGCATGCTG GTGCCTGAGC CTGTGTCCTC CTCCTCATGT TTACCAGGGA 360
GGTATATGTC AGGCACAGTG ATTGATCTAA CTGATGCTGG GAACAACAGT AACTACATTT 420
AGATGACTAT TTTTTTTTGT TTGGACAAGG TCTTGCTCTG TTGCCCAGGT TGGAGTGCAG 480
TGGTGCAATC ATGGCTCATT GCAGCCTCGA CCTCCTGGGC TCAAGCAATC CTCCCACCTC 540
AGCCTCCCAA AATAGTTGGG AGCACAGGTG CATGCCACCA CACCCAGCTA ATTTTTTTTT 600
TTTTTTTTTT TGAGATGGAG TTTTGCTCTG TCACCTGGCT GGAGTGCAAT GGCGTGATCT 660
CAGCTCACTG CAACCTCCGC CTCCCCGGCT CAAGCGATTC CCTTGTCTCA GCCTGCCAAG 720
TCGCTGCGAT TACAGGCACC CACCATCACT CCCGGCTAAT TTGTTTTGTA GTTTTTAGTA 780
GAGACGGGGT TTCACCATGT TGACCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCCT 840
CCTGCCTCGG CTTCCCAAAG TGCTGGGATT ACAAGCGTGA GCCACCGCAC CCAGCCACTA 900
ATTTTTTATT ATTTGTAGAG GTGAGGATCT CCCTGTGTTG CCCAGGCTGG TCTCGAACTC 960
CTGGCCTCAA GCCATCCTCC TGCAGCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGACC 1020
CACCGCGCCC AGCCTCAGCC TGGTTCCTTG CGTGAGTCTT GGTTTCTTGG TCTCCTTTTC 1080
CCCGTATGCC AGCTGCCTCC CTCCATAAGA GAACATCTGT GATGACCTTC GGGGTGCCCA 1140
CTTAGGCTTT CAAAGGGGCC TGGAATGTAG GGCACAGGGT AAGAGACTCG GACACCAGGC 1200
CTTGGGGAAA AGGAGAAGCG GGCCCATATG CCCTCCTCTC ACCCACAGGG AGCTGTGGCT 1260
TCGAAAGGGG CTCCTCCCTT GTAAGGCTGC TGCTCCTGTC GTCATGGAGG AAACCTTGGT 1320
TCTGCTTCCC TAGCACCCCA AACTGCAAAG TCACGCTGGC AGGTATTGCA CCCAGAGGGC 1380
TCATTCCCCA TTCATCATAG TCACTGGTTG GGCAAGTCAC CCTCCCTAGA AAGCGCAGCC 1440
TTGGGTAAAT CCACCAGACA TATCCTGATC TTTCACTATT CACAGAGCCA GACTGGAGTG 1500
GCCTTTCGTA ATGGCCCTGG CCAGAGCTCC CGGGGGAAGC CTTCCGGATA GGCAGCTTGT 1560
CAGCAAGAGT GGGAAACCCT GGGCTGCGCC CTCCCCACAA ACCACCAGCA TTGCCCAACT 1620
TCCTCTCTTC ATGCCCTCTA CCACCCTCTC GTTGCCCCAG CTTTCTTTCT TTCATTTTTT 1680
TTCTTGAGAC ACAGTTTCAC TGTCACCCAG GCTGGAGTGC AGTAGTGTGA TCTCGGCTCA 1740
CTGCTACCTA CCTCCACCTC CTGGGTTCAA GCGATTCTCA CACCTTAGCC TCCCGAGTGG 1800
CTGGGATTAC AGGCACGTGC CACCAACTCT GGCTAATTTT ATATTTTTAG TAGAAACAGG 1860
GTTTCACCAT GTTGGTCAAG CTGGTCTCAA ACTCCTGACC TCAAGTGTTT CATCTGCCTC 1920
AGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAGCTACCAC ACGTGGCTAA TTTTTGTATT 1980
TTCAGTAGAG ATGGGGGTTT CACCATGTTG GCCAGGCTGG TCTTGAACTC CTGACCCCAG 2040
GTGACCTGCC CTCCTCAGTC TCCCAAAGTG CCGGGATTAC AGGCATGAGC CACCGCACCC 2100
AGCTGTTTCC CCAGCTTTCT AACAGTGAGG TTAGTTTTGT CTCTTCTCTT TTATTAATAT 2160
ACTGCTACTT ATCTCCAATG ATCTGAAGAC TCAAGGTGGG TGATGCCTGA CTTACAGGAG 2220
ATCCCCCAGC ACGGGAACCA TCCCTTATCC AGCTCTGGGT CTCTTGCAGT GTCCAATTTC 2280
TAGAAGTGAC CTTTCTGTCA AGTGAATGAG CCAAGCCCCA GCCACATCCC AGCACTAGAA 2340
AACCTGATGC CTCTCCCTTG AGCACATCCT TTTTTTTTTC TTCCAAGTTT 2390