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

TagContent
EnhancerAtlas ID
HS095-07983 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr12:123335910-123338580 
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: 3             
IDChromosomeStartEnd
GH12I122850chr12123335349123336050
GH12I122851chr12123336141123337788
GH12I122853chr12123337886123342141
Enhancer Sequence
GAAAAAAGAA GACATGAGTG ATCAGACCAA CTGATCACTA TGAAATGACC CTGGCCAGCC 60
GCAGTGGCTC ACATCTGTAA TCCCAGCATT TTGGGAGGCC GAGGCAGGCA GATTGCTTGA 120
GGTCAGGGGT TCAAGACCAG CCTGGCCAAC ATGGTGAAAC CCTGTCTCTA CTAAAAAAAT 180
ATAAAAATTA GCCAGGCGTG GTGGCGCACG CCTGTATTCC CAGCTACTTG GGAGGCTGAG 240
GCAGGAGAAT CACTTGAACC TGGGCGGCGG AGATCATGCC GCTACACTCC AGCCTGGGCA 300
ACAGAGTGAG TCTCCGTCTT AAAAAAAAAA AAAAGAAAAA GAAATGCCCC TGCCCCTCCT 360
GGGGTCCCTG CACCTCCAGG GATAGGTAAT GGGGCCTCCT GGCCCCTCCA AAGCATGGCA 420
GGCCCCAGCG GGTACATCCA GGATACAGGT TCAGCCATCT CTTCCATCCA GTGAGTGTCA 480
CTCCATCAGC CCCAAGACAG GGAGGGTGAG GAGGTGTGCA CAGGAGCCAC CTTGCCAGGT 540
TCCTGCCCCA GCCTTGGGCC ATCTGCAGAG CCCAGCTGGA AGAAAGGTTT GGGTCGTCCT 600
GCCATTTTCT GCTCTAGAAA GCCTCTGAGT CACGTCAGAC TTCCTAGCGA GGGAACCCGG 660
CCGCTGTTGG ACAGGAAATC TCAGAGGGCT CAGCTTCCAG GCTGGAGAAC TGATTGTTCT 720
GGGTGGCAGC TTCAAAACAA CTCATGGGTG ACTCAGTGCT CTCCATAAGA GGGCAAGAAG 780
CAAATGCCTC CTTAAGGGAA AATTGGGAGT TAGAGGCAGT TTGGGCAGCC TCCCTGAGTC 840
CCCAGGTCTG GCCAGTGCAG CTGGGCGAGC CTGATGGGTA TTCAGTTCCA GTGGGTGGGA 900
GGTGGGCTCA GAGTTGGACC CTTGTGCCTG GGAAGAGCCT GCTCAGGATC TGACATGGAG 960
AGCAGAGGGC AGGTGTCCAA AGGTGTGGCC CCAACTGTGC AGCAGGACAG GGCTACCAGG 1020
CTCTGTGTCC TGGCAGAGAT GTGCTGAGCC TGAGCCTCTC AGCACAGAGC CCACCAGGTA 1080
GGAGCCAGTT ACCCCTGGCA TGGGAGAAGG CCAGTGTGGG CAGGCAGTGG CCCCACGAGG 1140
GAAGTGGAGA ACACTCACAG GCACGCTTCC CACCTGGTGA CGCTGGTGTG TTGATGAAGC 1200
ACAAATGGGG TGTACCAGCA TCTGCTGGAG AAATTCCCAG ATCTGCAGAG GTGACAGGTA 1260
CAGGGGCTTC CCTGCCTCAG GACCTGTAAC AGCAAAGAAA CACAAACGTC CTAAACATGC 1320
CTCAGCAGAG GCTGCGTCTC GCTGTCTGTG CAGAGCAGAG AACGGAGGGT GGTGGGAAGA 1380
GAGATGTGTC GAATCTGGGA TGGCCGGGAA GATCTAGAAA ACATTCTACT GTGTGAAATC 1440
AAGCAGATTG CCGAACAGCA TGGACATACG TGTTGAAGAT CCAAGCAGTA CTTTATGTGT 1500
GCTGTAATTT TTTGCAAGGA AAACATACTT AGCATGACAT GTAATTAGAG ATTACTTTTT 1560
TAAAAAGGCA AGGGGCGGCA CTTTGTGTCT TCCTTCTTGC CCCTCCCCCC CAGGCTCTCT 1620
CCTGTCACTG CAGAGATTTG CAAGTGGTCC CATCACAGGC AAGGCAGGAG CAGGACCTGA 1680
GGGGCCAGGG CACAGGTCTG TGCAGCGGGG GCTGTCTGGC CGCTCTCCCG TGCTGGCCAG 1740
CTGCCTGCTC TTTGTCATTC TCTCTGCCCC AGAGAAGCTG CCAGCCAAGG AGGAGGCAGC 1800
CTCATGTTTG TCCTTTGTCC CTCCCACTTG GTAGTTCTGA TACAAGGCCC GATTGTCAGG 1860
GGCAGGGGAG ACGGGCCCTG GGGGTGTCAG GGGCAGGGGA GACGGGCCCT GGGGGTGTCA 1920
GGGGCAGGGG AGACGGGCCC TGGGGGTGTC AGGGGCAGGG GAGACGGGCC CTGGGGGTGT 1980
CAGGGGCAGG GGAGACGGGC CCTGGGGGTG TCAGGGGCAG GGGAGACGGG CCCTGGGGGT 2040
GTCAGGGGCA GGGGAGACGG GCCCTGGGGG TGTCAGGGGC AGGGGAGACG GGCCCTGGGG 2100
GTGTCAGGGG CAGGGGAGAC GGGCCCTGGG GGTGTCAGGG GCAGGGGAGA CGGGCCCTGG 2160
GGGTGTCAGG GGCAGGGGAG ATGGGCCCTG GGGGCAAGCG AGGTTTCAGG GTCACTTGGG 2220
GTGTGCAGAG CCAAGCTGTG ACCCTAGTGC CGTGTTACTT GGCAGAAGCC CTGCCTGTTC 2280
CCACATCTGT AAAGTTAGGC ATTTGGGGTG CTCCATCGTG AGCCTCCTTC CTGCTCTAAC 2340
ATTCAGCGTG GGTTTGAGGC CCGTGGGCAT GGAGCTATCC GTCACCCTTG TCAGTCGGGC 2400
ACCTCGTCCT GGGCTCCCAG GTGGAGGTCT CTGGAAGCCC TTGCTGAGCT GGGCTGGGAG 2460
CTCCTTTGCC CTGACCTTGT TGTTGCCGTT GACCTCCTTC ATGGGAGCAT CTGGTCTTGA 2520
CCTGGGGCAG CCACCAGCAC ATGAGGCTCC CGTCTTGGAG GCAGGGGGCA CACTGGTGTG 2580
TGGGAGCTGG CTTAGGGCCC TGCTTCACAG TTGGACCACC TTGGACAGGT TGCCCAGCTC 2640
CCAAGGGCTC ACGTTCTTCC TCCTGCCCCT 2670