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

TagContent
EnhancerAtlas ID
HS061-06048 
Organism
Homo sapiens 
Tissue/cell
GM12892 
Coordinate
chr12:113666580-113668780 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr12:113666695-113666706AGGGTGTGGCT-6.02
NFKB1MA0105.4chr12:113667794-113667807CGGTGAATCCCCT-6.24
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00883chr12:113664391-113671759Adrenal_Gland
SE_01635chr12:113664281-113667458Aorta
SE_01635chr12:113668074-113671857Aorta
SE_04226chr12:113666509-113667424Brain_Anterior_Caudate
SE_04226chr12:113668219-113671573Brain_Anterior_Caudate
SE_05290chr12:113664454-113667544Brain_Cingulate_Gyrus
SE_05290chr12:113668185-113671971Brain_Cingulate_Gyrus
SE_06123chr12:113664483-113668557Brain_Hippocampus_Middle
SE_07164chr12:113664435-113667544Brain_Hippocampus_Middle_150
SE_07164chr12:113668204-113672804Brain_Hippocampus_Middle_150
SE_08283chr12:113664441-113667611Brain_Inferior_Temporal_Lobe
SE_09783chr12:113664182-113681103CD14
SE_23178chr12:113667524-113667944Colon_Crypt_1
SE_24018chr12:113667561-113667905Colon_Crypt_2
SE_26345chr12:113666385-113667518Duodenum_Smooth_Muscle
SE_26677chr12:113664465-113671657Esophagus
SE_27860chr12:113666514-113670777Fetal_Intestine
SE_28798chr12:113666400-113670853Fetal_Intestine_Large
SE_29890chr12:113664319-113667465Fetal_Muscle
SE_37095chr12:113664640-113672337HSMMtube
SE_40725chr12:113664070-113673220Left_Ventricle
SE_42290chr12:113664247-113673161Lung
SE_48084chr12:113663861-113673266Psoas_Muscle
SE_48792chr12:113664080-113667427Right_Atrium
SE_48792chr12:113667499-113671975Right_Atrium
SE_49644chr12:113668214-113668917Right_Ventricle
SE_50157chr12:113666365-113667434Sigmoid_Colon
SE_50157chr12:113667477-113668047Sigmoid_Colon
SE_51183chr12:113663840-113675194Skeletal_Muscle
SE_52527chr12:113666312-113668153Small_Intestine
SE_52527chr12:113668194-113669763Small_Intestine
SE_53751chr12:113665943-113668697Spleen
SE_60802chr12:113634217-113672070DHL6
SE_61851chr12:113631410-113672028Toledo
SE_65505chr12:113666921-113667902Pancreatic_islets
SE_65505chr12:113667937-113672747Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12113667617113667862
Number: 1             
IDChromosomeStartEnd
GH12I113226chr12113664004113672117
Enhancer Sequence
TTTCCTCCCA CACCACAGTG GAAGGCGCTT TGGGGAAAGG GATGAAAGTG ATTGTGGCTC 60
AGTTTCAGCT TTAGAGAGGA ATGCTGCCTA GTGAGGGAGG GTGGTTGGCC TACTAAGGGT 120
GTGGCTTGTG TCTGGAAATA GCCAGGCTTA AGATTCTAAA TGGGAATCCT GGCTGTCATC 180
GTGAGTGTCA CTTTTAAGTC CCTCCAACGT GCCTGACCTG ATGGTGGGGT GTCCAGCTTT 240
CCTGTGGGAT GAAAGGGGCA AGAGAGCAAC CCAGTCCTGT GTCAAGATCA GGCTTTGAAT 300
GTTGATGAAT AGGAAATAGG CCAGAGACAC AATAAGACTC CCCTTGGCTA GGCCACTAGC 360
AAGGCTGCTT TTATCTTGGC AAAGTCAGTG GCTTGCTTTG GTTTGTTTCT CAAGAATAAA 420
GAAATGTATA ACTAACTGCT GGGGTCCAGG GACATTGTTT TTCCTGTACA GCACATTAGT 480
ATCTTAGTTT CTTCTCTCAG CTTCTTACTG GGTCATTTTT TAAAACCTCA ATGACTTGTG 540
GGTGTAATTC ACCAAGCCTG GCTGGGAAGA AGGGTAGGAC CTGTGCAAGT AAACAAGAGT 600
TTTCAGAGGA GGCCTGCTCT GCCTTAGCAT AGTAGGCCTT TGATATTTCA TGCTTGGATT 660
TTGGCCTTGA CCTTCTACCC CAGCGTCCCC CTGTCCCTGC TGTCTGAGGA GCAGTCCTTC 720
AGTCCTTTTT TTTGAGACAG TCTCGTTCTG CTACCCAGGC TAGAGTGCAG TGGCACAATC 780
TCGGCTCATT GCAACCTCCG CCTCCCGTGT TCAAGCAATT CTCCTGCCTC AGCCTCCCAA 840
GTAGCTGGGA TTACAGGCGT GAGCCACTAC ACCCAGCTAA TTTTTTTGTA TTTTTAGTGG 900
AGACGGGGGT TTTACCATGT TGGCCAGGCT GGTCTCGAAC TGTTGGCCTC AAGTGATCCA 960
CCTGCCTCGG CCTCCCAAAG TGCTAGGATT ATAGGCGTGA GCCACCACAC CCGGCCCTGA 1020
GCAGTCCATC TAAAACACAA GCCCAACCTG GTTGTTGCCT TGTTTTAAAG CTTCCTGGGA 1080
CTTTCCCATC CCTCTATGGG GGTTGGGGAG GGCAAGCTCT TCAGCTGGCA ACGAAGCCTT 1140
GCGTGTTCTA GTGCCTTCTT GCTTGACCAG TCCCATTTCC TGCCTCAGTC CACAGCATCA 1200
TACTGCATTT AGTTCGGTGA ATCCCCTGTG CATTCTTAAA CCTTTCCACC TTGCTGGCAA 1260
GTCAGTCTAG AATCCCTTTC TCAGCCTCTT GTTTGCTCGT GGCCTCCAGT TCTGTCTTGA 1320
AAATCCTGCT GATAACACCA TCTCTTTGAA GCCTTCACTG AACTTCCCCT TCCTGACAGA 1380
GCTAATTACT CACTACCCTT TTCTGCTTCG GTATCTTGAT TAGGCTTCCA TTATTACAAG 1440
TAGATTATAG TGGGGTAATT ACACATTTAA CCATCTGATC ACCTACTAGG CCCTGAGATC 1500
CATTCATCTT TTTTTTTTTT TTTTTTTTTT TGAGGTGGAG TATCACTCTG TCACCCAGGC 1560
TGGAGTGCAG TGGCACCATC TCAGTTCACT GCAACCTCCA CCTCCCAGGT TCAAGTGATC 1620
CTCCCACCTC AGCAGCTGAG ACTACAGGCA TGTGTCACCA CGCCCAGCTA ATTTTTTGTA 1680
TTTTCAGTAG AGCCTCTTTC CTTGGCTCCC AAATGGTTAC CTTTTTGCTG TGTCCCCACG 1740
TGATTGTCCC TGAGTCTGTG TGTCTGTCCT CTTCTGATAA AGACACCAGT CCTATTGGAT 1800
TAGAGCTCAT CCATATGACC TTGTTTTATC TTAGTCACCT TTAAAGGCCC TTTCTCCAAA 1860
CACAGTCACA TTCTTTCACC ATGTTGGCCA GGCTGATCTC AAATTCCTGA CCTCGAGTGA 1920
TCTATCCGCC TTGGCCTCCT GAAGCGCTGG GATTACAGGC ATGAGCCACC ATGCCTGGCC 1980
CATCCATTTG TCTTTGTATC ACATAGCTCA GTGCCCACAA TATGCAGGTA CTCAACAAAT 2040
AGTGGTCAGA ATCAACGTAC TTGGATTTCT GGGGCCTCGC AGCCCATGGG AGTGGCAGTG 2100
TAAGGGCCCG AGTTAGAGGT GGGCAGCCTC CCTCCTGCCG CCTCTCCTCA CCATTGCTTT 2160
GAGTCCCATT GCTCTCAGCA CAGCTGAGTG TCCTGGTGGC 2200