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

TagContent
EnhancerAtlas ID
HS196-05781 
Organism
Homo sapiens 
Tissue/cell
ZR75-1 
Coordinate
chr10:71217520-71220660 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17490626chr1071218646hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXA1MA0148.4chr10:71219004-71219020CATTAAGTCAACAAAT+6.25
ZNF740MA0753.2chr10:71219675-71219688ACCCCCCCCCCAC+6.32
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00177chr10:71208884-71237023Adipose_Nuclei
SE_03334chr10:71217415-71218032Brain_Angular_Gyrus
SE_03334chr10:71218308-71218883Brain_Angular_Gyrus
SE_04154chr10:71216588-71221786Brain_Anterior_Caudate
SE_04937chr10:71216635-71221777Brain_Cingulate_Gyrus
SE_05904chr10:71216127-71221923Brain_Hippocampus_Middle
SE_06878chr10:71216373-71221571Brain_Hippocampus_Middle_150
SE_07975chr10:71216588-71219267Brain_Inferior_Temporal_Lobe
SE_07975chr10:71219700-71221941Brain_Inferior_Temporal_Lobe
SE_23286chr10:71216337-71220954Colon_Crypt_1
SE_23928chr10:71216637-71218016Colon_Crypt_2
SE_23928chr10:71218190-71219803Colon_Crypt_2
SE_23928chr10:71219805-71220891Colon_Crypt_2
SE_25858chr10:71215901-71220911Duodenum_Smooth_Muscle
SE_29794chr10:71219457-71221699Fetal_Muscle
SE_31566chr10:71215830-71221796Gastric
SE_41723chr10:71216331-71218193LNCaP
SE_41723chr10:71218269-71221688LNCaP
SE_42468chr10:71216218-71221922Lung
SE_47339chr10:71216946-71219518Panc1
SE_47339chr10:71220244-71221480Panc1
SE_48249chr10:71215999-71221926Psoas_Muscle
SE_49437chr10:71219259-71221866Right_Atrium
SE_50329chr10:71216303-71221673Sigmoid_Colon
SE_51407chr10:71215733-71221961Skeletal_Muscle
SE_52896chr10:71216217-71221726Small_Intestine
SE_54066chr10:71216709-71218767Spleen
SE_54066chr10:71218864-71221937Spleen
SE_54616chr10:71216909-71221726Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 6             
ChromosomeStartEnd
chr107121980971220461
chr107121758171217684
chr107121823271219262
chr107121928571219384
chr107121880071219652
chr107121802671218168
Number: 1             
IDChromosomeStartEnd
GH10I069456chr107121632571221892
Enhancer Sequence
AACTTCCATG CACCTAACCT ACCTGAAGAG TTGCTAAGCA GATTAGATGG ATTAATACAT 60
CTGAAGAGCT TAGAGTGGTG CCTGGCACAT GATGAACACT CCATCAACTA GTCATGGATT 120
AGTCGTTCTT TTCCTGCCTT CCTCTCTAGC CTTGCTGCTC AAGAGCCATA GACTAAGAAT 180
GAGAAGGGCT GTTAAAGACA CCTCTAGTGC AGCCTTTTAA ATTTACCGAT AAGAAATCAG 240
AGGCCTGAAG AGAAGTGAGT TGCCTGAAAG CCCACAGCAA GTCAGTGACA GGCCAAGACC 300
AGATCCAGGC TGCCTGACTC CAGTTTCTTC CTCGGGCCCC CATGACCTTT CCAGGCGCCA 360
TGTATGTTTC TCCCTGGTCT CAGGGTGAGG GTAGAAGATA ACCTTTCTGA AAGAGGCCAC 420
GTCCCTGGCC TCCCAGTGAA GCACTAGGTG AAGCCAGGCC AAAAAGAAAG CACTTCTCTG 480
GAGACAGTTT CCAGGAGATT TTTACTTTCG AGAAGAGCTT TATTATTTTT GTGAAAATCA 540
TACATGCGCA TAGCTTAAAA GATTCAAGCC ATTTGGGAAA GTACAACGAA AACAGCAAAA 600
GTCCCCTTTG ATTCTACCAC TGGGATTCAG CCACTGTTAT ATGTTGGTAA ACATCCATCT 660
GGACATCTTG TACATATATG TAGACATTTT ATTTCTTTAA TTATCTTTCT TATTGTGTTT 720
GATTTGTCGA GCAAAGTTCA TTTTCTGGCT CTAGGTAAGC ATTCCAAATA GTGAAACTCA 780
AATAGTGAAG CTGAAAGTGG GGCAGCCTTC ATATTGGAGA AGTGGCCAGC CGTGCCTAAC 840
GGGCTGTCAG AGATGATCTC ATAGCATCAG ACTGGGCTCA GGCCTCGGGC ACAGAGAGGT 900
CCTCCCCTCC CCCAGTCTGG CCACAGAGCC TTTAAAATCC AGAGAATCAG GGCTGCAGCC 960
CTGCCAGGGG TTTGGAGAAC CTTCCAACAC CTTCATTTTA TAGATGAGCA AACTAAGGCC 1020
CTGAGAAGTG TCCTTCGCTC TTAACCTAGA CTTTGTACAT GGTCTCGTTC CCCGCTTTAA 1080
TAGAGGAATT GCTTTATGTC GTAGGACTGG ACCTTGCTGC CTTTGGGTTG GTTCCTGGAG 1140
AAGCAGGAAT AACCACCTGC CCTCCTGCCC GGAGGCCTTT CTTCCCAGGT GACTCACAGT 1200
GCCACCCTGG GGTGGGGCTC ACGGTCAACC TGATAAGGGA CTGATAATGA AATTTCTGTA 1260
CCAACTGGCT CCACACAGGG GAAAGATGTT TTCTGGGTAA GTCTGGTCAG AAGAGGTTGA 1320
TGGGGGGAAA ACAAAACAGA CAAAAAAAAA AAAAAAAAAA ACAACAACAA AACAACCTTT 1380
CCCAGAGAGA ACTTTTAGAT GTGAATGGGT TTGAATTGAC TTCTTGTTGG AAGGCAGGAG 1440
CATTCAGTCT TAACCAGCCG TGCTCTCTGG TTGGTTGGTT TGTTCATTAA GTCAACAAAT 1500
AGTTATTTGA TGCCTACTGA ATGCCAGGCA CTGTGATACC GTGATAGGTG TGGGAAGCAA 1560
CTATGAACAA GACAGGTTTA GTCCAGGCCT TGGAAGACAG AGCAGTAAAT AAATATCACT 1620
TGTGATAGGT GCTAAGGAGA AAATTAGGGA GCAAGTGGGG AGGGATGGGC GTTTCCACTT 1680
TCGATGATGT GGTCAGGGAA AGCCTTTATG AGGAGCTGAC ATTTCAGCTG AAGCTCAAAT 1740
AGAGAAGGAG CCAGCCATAA AGACTTGTCC AGAGCATCCC AGGCAGAGAG AGCCATGAGT 1800
TCAAAGTCCC TGAGGCAGGT CGCAAGCATG GCTACAGCAG ATGAGGAAGC CCGGGAAGGG 1860
CTGCGCTGTG GGTGGAGAGG GTGGCAGGGG CCTGGCTGTG TGAAGAGTTT GGGGTTCGAG 1920
TGACTGAGAA GCAGGGTTTC ATTGTCAGGC CCTGTGGTCT TGCCATCCAG AGACCTAGAT 1980
CAGGTGTTGG CTATTCTGTG TGACACTGGG TAAAGGACCA GCTCTCTGAG CCTCCGAGAT 2040
GCCTCCTCTG TGGGTACCCC AGAGGGCAGT GGGGAGGATC CTGTGAGATG AGAGGTGCCA 2100
AAGCACGGGG CCTACTCTAG GGTCCCCCAC CCACGGAGGG AGGGAGACTC TAGGCACCCC 2160
CCCCCCACGA ATGGAGGGAG ACTCTAGGGC TCCCTGCCCA CGGAGGGAGG GAGAGTCACC 2220
TGGGAGCCTT GCATTGCTCA GGGGTAGTTG GGGAGATGAG ATGAGATGAG ATGAGATGAG 2280
ATGAGATGAG ATGAGATGAG ATGAGAACCT CTGGAATCCG TCTTGTCAGA GGAGGCTCCT 2340
TTGCCCCTGG GGGTACTCAG CCTGCCTAGA ACAGATGGCT ATGGAACCAA CTCCTCCAGC 2400
CAGCTGGTCT GACCCCTAGG GTGTGCATGT GGTCTTTTCC AGAGGCTGGG CCCCTCCCAC 2460
CCCTTAGTTT CTGGGCTACC ATGGCACACT GTCAGAAGCA CTAGGCCACA ACAGGCACGC 2520
GGGGCCAGGC AGGCCGTCTG AGAAGTGTCC TGCTAGGCTC TGAGGGGTCC CAGCCCTCGG 2580
TCAGCATGAG TTGTTCAGCT CCAAGCTAGG CCCCTGGGCT GGTGGAGGTG AGGAAGAGAC 2640
ACCGTAGAGA CACTGTAGAC TTACGATGTC ACCTTCCCCA GCTAGAGGGT TGGCCTGTGA 2700
AGGAGCTGGC AGCCATCTCT GCCTCTGGCG ATGTGCCATG TTAGCCCAGG AACTAAGGGG 2760
TGGGAAGGGC CCAGTCCCTG GAAAAGACCA CATGCACGCC CAAGGGGTCA GACCAGCTGG 2820
CTGGAGGAGC TGGTTCCATC AAGGGCCAGT CTGAGCTAGG CTGCCTGACT GTGGTGGCCT 2880
GACCACCACA TTTTGCTTCA TCTCTTTGGA TTCTCAGAGT GACCCTTGAG CTGGGCTGGA 2940
CAGGGGGTCT TGTCCTGTTT TACAGAGGAG TCTTTGGGAG GACTCTGAGG GCTTCACTGG 3000
GCAGGGAGGC CTCGCAGAGA GGAGTGGAGA TGAGTCTTAG GAGAGGGAGG GCGGGCTACA 3060
GAATGTTTTT TGGGCCTGAG TGTTGAGGTC AGAAATGTCC TCTGGGAAGA CCAGGTCTGG 3120
AGGCCAAGCA GAGCTGAGGA 3140