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

TagContent
EnhancerAtlas ID
HS145-06308 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr12:123336130-123338580 
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: 2             
IDChromosomeStartEnd
GH12I122851chr12123336141123337788
GH12I122853chr12123337886123342141
Enhancer Sequence
CAGCTACTTG GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGCGGCGG AGATCATGCC 60
GCTACACTCC AGCCTGGGCA ACAGAGTGAG TCTCCGTCTT AAAAAAAAAA AAAAGAAAAA 120
GAAATGCCCC TGCCCCTCCT GGGGTCCCTG CACCTCCAGG GATAGGTAAT GGGGCCTCCT 180
GGCCCCTCCA AAGCATGGCA GGCCCCAGCG GGTACATCCA GGATACAGGT TCAGCCATCT 240
CTTCCATCCA GTGAGTGTCA CTCCATCAGC CCCAAGACAG GGAGGGTGAG GAGGTGTGCA 300
CAGGAGCCAC CTTGCCAGGT TCCTGCCCCA GCCTTGGGCC ATCTGCAGAG CCCAGCTGGA 360
AGAAAGGTTT GGGTCGTCCT GCCATTTTCT GCTCTAGAAA GCCTCTGAGT CACGTCAGAC 420
TTCCTAGCGA GGGAACCCGG CCGCTGTTGG ACAGGAAATC TCAGAGGGCT CAGCTTCCAG 480
GCTGGAGAAC TGATTGTTCT GGGTGGCAGC TTCAAAACAA CTCATGGGTG ACTCAGTGCT 540
CTCCATAAGA GGGCAAGAAG CAAATGCCTC CTTAAGGGAA AATTGGGAGT TAGAGGCAGT 600
TTGGGCAGCC TCCCTGAGTC CCCAGGTCTG GCCAGTGCAG CTGGGCGAGC CTGATGGGTA 660
TTCAGTTCCA GTGGGTGGGA GGTGGGCTCA GAGTTGGACC CTTGTGCCTG GGAAGAGCCT 720
GCTCAGGATC TGACATGGAG AGCAGAGGGC AGGTGTCCAA AGGTGTGGCC CCAACTGTGC 780
AGCAGGACAG GGCTACCAGG CTCTGTGTCC TGGCAGAGAT GTGCTGAGCC TGAGCCTCTC 840
AGCACAGAGC CCACCAGGTA GGAGCCAGTT ACCCCTGGCA TGGGAGAAGG CCAGTGTGGG 900
CAGGCAGTGG CCCCACGAGG GAAGTGGAGA ACACTCACAG GCACGCTTCC CACCTGGTGA 960
CGCTGGTGTG TTGATGAAGC ACAAATGGGG TGTACCAGCA TCTGCTGGAG AAATTCCCAG 1020
ATCTGCAGAG GTGACAGGTA CAGGGGCTTC CCTGCCTCAG GACCTGTAAC AGCAAAGAAA 1080
CACAAACGTC CTAAACATGC CTCAGCAGAG GCTGCGTCTC GCTGTCTGTG CAGAGCAGAG 1140
AACGGAGGGT GGTGGGAAGA GAGATGTGTC GAATCTGGGA TGGCCGGGAA GATCTAGAAA 1200
ACATTCTACT GTGTGAAATC AAGCAGATTG CCGAACAGCA TGGACATACG TGTTGAAGAT 1260
CCAAGCAGTA CTTTATGTGT GCTGTAATTT TTTGCAAGGA AAACATACTT AGCATGACAT 1320
GTAATTAGAG ATTACTTTTT TAAAAAGGCA AGGGGCGGCA CTTTGTGTCT TCCTTCTTGC 1380
CCCTCCCCCC CAGGCTCTCT CCTGTCACTG CAGAGATTTG CAAGTGGTCC CATCACAGGC 1440
AAGGCAGGAG CAGGACCTGA GGGGCCAGGG CACAGGTCTG TGCAGCGGGG GCTGTCTGGC 1500
CGCTCTCCCG TGCTGGCCAG CTGCCTGCTC TTTGTCATTC TCTCTGCCCC AGAGAAGCTG 1560
CCAGCCAAGG AGGAGGCAGC CTCATGTTTG TCCTTTGTCC CTCCCACTTG GTAGTTCTGA 1620
TACAAGGCCC GATTGTCAGG GGCAGGGGAG ACGGGCCCTG GGGGTGTCAG GGGCAGGGGA 1680
GACGGGCCCT GGGGGTGTCA GGGGCAGGGG AGACGGGCCC TGGGGGTGTC AGGGGCAGGG 1740
GAGACGGGCC CTGGGGGTGT CAGGGGCAGG GGAGACGGGC CCTGGGGGTG TCAGGGGCAG 1800
GGGAGACGGG CCCTGGGGGT GTCAGGGGCA GGGGAGACGG GCCCTGGGGG TGTCAGGGGC 1860
AGGGGAGACG GGCCCTGGGG GTGTCAGGGG CAGGGGAGAC GGGCCCTGGG GGTGTCAGGG 1920
GCAGGGGAGA CGGGCCCTGG GGGTGTCAGG GGCAGGGGAG ATGGGCCCTG GGGGCAAGCG 1980
AGGTTTCAGG GTCACTTGGG GTGTGCAGAG CCAAGCTGTG ACCCTAGTGC CGTGTTACTT 2040
GGCAGAAGCC CTGCCTGTTC CCACATCTGT AAAGTTAGGC ATTTGGGGTG CTCCATCGTG 2100
AGCCTCCTTC CTGCTCTAAC ATTCAGCGTG GGTTTGAGGC CCGTGGGCAT GGAGCTATCC 2160
GTCACCCTTG TCAGTCGGGC ACCTCGTCCT GGGCTCCCAG GTGGAGGTCT CTGGAAGCCC 2220
TTGCTGAGCT GGGCTGGGAG CTCCTTTGCC CTGACCTTGT TGTTGCCGTT GACCTCCTTC 2280
ATGGGAGCAT CTGGTCTTGA CCTGGGGCAG CCACCAGCAC ATGAGGCTCC CGTCTTGGAG 2340
GCAGGGGGCA CACTGGTGTG TGGGAGCTGG CTTAGGGCCC TGCTTCACAG TTGGACCACC 2400
TTGGACAGGT TGCCCAGCTC CCAAGGGCTC ACGTTCTTCC TCCTGCCCCT 2450