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

TagContent
EnhancerAtlas ID
HS139-14036 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr12:123335840-123338570 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10744422chr12123336789hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr12:123336655-123336666GGGTGACTCAG+6.02
JUNBMA0490.1chr12:123336655-123336666GGGTGACTCAG+6.02
NFICMA0161.2chr12:123338165-123338176TACTTGGCAGA+6.62
ZNF263MA0528.1chr12:123337498-123337519CTTCCTTCTTGCCCCTCCCCC-6.21
Number of super-enhancer constituents: 22             
IDCoordinateTissue/cell
SE_01099chr12:123336164-123337356Adrenal_Gland
SE_03273chr12:123336253-123337789Brain_Angular_Gyrus
SE_03273chr12:123337998-123338820Brain_Angular_Gyrus
SE_03969chr12:123335192-123341496Brain_Anterior_Caudate
SE_04866chr12:123335187-123348510Brain_Cingulate_Gyrus
SE_05835chr12:123320384-123351312Brain_Hippocampus_Middle
SE_06752chr12:123320303-123342892Brain_Hippocampus_Middle_150
SE_07820chr12:123320283-123343131Brain_Inferior_Temporal_Lobe
SE_08837chr12:123336567-123337265Brain_Mid_Frontal_Lobe
SE_08837chr12:123338112-123338556Brain_Mid_Frontal_Lobe
SE_26757chr12:123336076-123337829Esophagus
SE_31427chr12:123336079-123337814Gastric
SE_31427chr12:123338001-123338893Gastric
SE_35883chr12:123336155-123337498HMEC
SE_40937chr12:123336044-123337543Left_Ventricle
SE_41807chr12:123338007-123338583LNCaP
SE_42306chr12:123335315-123337685Lung
SE_42306chr12:123337992-123338858Lung
SE_49030chr12:123336074-123337640Right_Atrium
SE_50159chr12:123336170-123337444Sigmoid_Colon
SE_65302chr12:123335214-123337685Pancreatic_islets
SE_65302chr12:123337885-123342137Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12123338145123338297
chr12123336382123337770
Number: 3             
IDChromosomeStartEnd
GH12I122850chr12123335349123336050
GH12I122851chr12123336141123337788
GH12I122853chr12123337886123342141
Enhancer Sequence
TCAGGTGAGC CGTAAAGAGG GGATGCGGGG GTCTGAGTGT ATTGCTAAGT CCCCAGAGAT 60
GGGACGAGAA GAAAAAAGAA GACATGAGTG ATCAGACCAA CTGATCACTA TGAAATGACC 120
CTGGCCAGCC GCAGTGGCTC ACATCTGTAA TCCCAGCATT TTGGGAGGCC GAGGCAGGCA 180
GATTGCTTGA GGTCAGGGGT TCAAGACCAG CCTGGCCAAC ATGGTGAAAC CCTGTCTCTA 240
CTAAAAAAAT ATAAAAATTA GCCAGGCGTG GTGGCGCACG CCTGTATTCC CAGCTACTTG 300
GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGCGGCGG AGATCATGCC GCTACACTCC 360
AGCCTGGGCA ACAGAGTGAG TCTCCGTCTT AAAAAAAAAA AAAAGAAAAA GAAATGCCCC 420
TGCCCCTCCT GGGGTCCCTG CACCTCCAGG GATAGGTAAT GGGGCCTCCT GGCCCCTCCA 480
AAGCATGGCA GGCCCCAGCG GGTACATCCA GGATACAGGT TCAGCCATCT CTTCCATCCA 540
GTGAGTGTCA CTCCATCAGC CCCAAGACAG GGAGGGTGAG GAGGTGTGCA CAGGAGCCAC 600
CTTGCCAGGT TCCTGCCCCA GCCTTGGGCC ATCTGCAGAG CCCAGCTGGA AGAAAGGTTT 660
GGGTCGTCCT GCCATTTTCT GCTCTAGAAA GCCTCTGAGT CACGTCAGAC TTCCTAGCGA 720
GGGAACCCGG CCGCTGTTGG ACAGGAAATC TCAGAGGGCT CAGCTTCCAG GCTGGAGAAC 780
TGATTGTTCT GGGTGGCAGC TTCAAAACAA CTCATGGGTG ACTCAGTGCT CTCCATAAGA 840
GGGCAAGAAG CAAATGCCTC CTTAAGGGAA AATTGGGAGT TAGAGGCAGT TTGGGCAGCC 900
TCCCTGAGTC CCCAGGTCTG GCCAGTGCAG CTGGGCGAGC CTGATGGGTA TTCAGTTCCA 960
GTGGGTGGGA GGTGGGCTCA GAGTTGGACC CTTGTGCCTG GGAAGAGCCT GCTCAGGATC 1020
TGACATGGAG AGCAGAGGGC AGGTGTCCAA AGGTGTGGCC CCAACTGTGC AGCAGGACAG 1080
GGCTACCAGG CTCTGTGTCC TGGCAGAGAT GTGCTGAGCC TGAGCCTCTC AGCACAGAGC 1140
CCACCAGGTA GGAGCCAGTT ACCCCTGGCA TGGGAGAAGG CCAGTGTGGG CAGGCAGTGG 1200
CCCCACGAGG GAAGTGGAGA ACACTCACAG GCACGCTTCC CACCTGGTGA CGCTGGTGTG 1260
TTGATGAAGC ACAAATGGGG TGTACCAGCA TCTGCTGGAG AAATTCCCAG ATCTGCAGAG 1320
GTGACAGGTA CAGGGGCTTC CCTGCCTCAG GACCTGTAAC AGCAAAGAAA CACAAACGTC 1380
CTAAACATGC CTCAGCAGAG GCTGCGTCTC GCTGTCTGTG CAGAGCAGAG AACGGAGGGT 1440
GGTGGGAAGA GAGATGTGTC GAATCTGGGA TGGCCGGGAA GATCTAGAAA ACATTCTACT 1500
GTGTGAAATC AAGCAGATTG CCGAACAGCA TGGACATACG TGTTGAAGAT CCAAGCAGTA 1560
CTTTATGTGT GCTGTAATTT TTTGCAAGGA AAACATACTT AGCATGACAT GTAATTAGAG 1620
ATTACTTTTT TAAAAAGGCA AGGGGCGGCA CTTTGTGTCT TCCTTCTTGC CCCTCCCCCC 1680
CAGGCTCTCT CCTGTCACTG CAGAGATTTG CAAGTGGTCC CATCACAGGC AAGGCAGGAG 1740
CAGGACCTGA GGGGCCAGGG CACAGGTCTG TGCAGCGGGG GCTGTCTGGC CGCTCTCCCG 1800
TGCTGGCCAG CTGCCTGCTC TTTGTCATTC TCTCTGCCCC AGAGAAGCTG CCAGCCAAGG 1860
AGGAGGCAGC CTCATGTTTG TCCTTTGTCC CTCCCACTTG GTAGTTCTGA TACAAGGCCC 1920
GATTGTCAGG GGCAGGGGAG ACGGGCCCTG GGGGTGTCAG GGGCAGGGGA GACGGGCCCT 1980
GGGGGTGTCA GGGGCAGGGG AGACGGGCCC TGGGGGTGTC AGGGGCAGGG GAGACGGGCC 2040
CTGGGGGTGT CAGGGGCAGG GGAGACGGGC CCTGGGGGTG TCAGGGGCAG GGGAGACGGG 2100
CCCTGGGGGT GTCAGGGGCA GGGGAGACGG GCCCTGGGGG TGTCAGGGGC AGGGGAGACG 2160
GGCCCTGGGG GTGTCAGGGG CAGGGGAGAC GGGCCCTGGG GGTGTCAGGG GCAGGGGAGA 2220
CGGGCCCTGG GGGTGTCAGG GGCAGGGGAG ATGGGCCCTG GGGGCAAGCG AGGTTTCAGG 2280
GTCACTTGGG GTGTGCAGAG CCAAGCTGTG ACCCTAGTGC CGTGTTACTT GGCAGAAGCC 2340
CTGCCTGTTC CCACATCTGT AAAGTTAGGC ATTTGGGGTG CTCCATCGTG AGCCTCCTTC 2400
CTGCTCTAAC ATTCAGCGTG GGTTTGAGGC CCGTGGGCAT GGAGCTATCC GTCACCCTTG 2460
TCAGTCGGGC ACCTCGTCCT GGGCTCCCAG GTGGAGGTCT CTGGAAGCCC TTGCTGAGCT 2520
GGGCTGGGAG CTCCTTTGCC CTGACCTTGT TGTTGCCGTT GACCTCCTTC ATGGGAGCAT 2580
CTGGTCTTGA CCTGGGGCAG CCACCAGCAC ATGAGGCTCC CGTCTTGGAG GCAGGGGGCA 2640
CACTGGTGTG TGGGAGCTGG CTTAGGGCCC TGCTTCACAG TTGGACCACC TTGGACAGGT 2700
TGCCCAGCTC CCAAGGGCTC ACGTTCTTCC 2730