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

TagContent
EnhancerAtlas ID
HS187-06311 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr12:113666500-113668940 
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: 38             
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_06123chr12:113668589-113673221Brain_Hippocampus_Middle
SE_07164chr12:113664435-113667544Brain_Hippocampus_Middle_150
SE_07164chr12:113668204-113672804Brain_Hippocampus_Middle_150
SE_08283chr12:113664441-113667611Brain_Inferior_Temporal_Lobe
SE_08283chr12:113668652-113671919Brain_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
TTTTACAGAG GAGGAGACAG GCTCAGAGAG GTTAAGTGAC TTGTCCAAGG TCACACAGCT 60
AGTAAGCAGT AAAGCCTGTC TTTCCTCCCA CACCACAGTG GAAGGCGCTT TGGGGAAAGG 120
GATGAAAGTG ATTGTGGCTC AGTTTCAGCT TTAGAGAGGA ATGCTGCCTA GTGAGGGAGG 180
GTGGTTGGCC TACTAAGGGT GTGGCTTGTG TCTGGAAATA GCCAGGCTTA AGATTCTAAA 240
TGGGAATCCT GGCTGTCATC GTGAGTGTCA CTTTTAAGTC CCTCCAACGT GCCTGACCTG 300
ATGGTGGGGT GTCCAGCTTT CCTGTGGGAT GAAAGGGGCA AGAGAGCAAC CCAGTCCTGT 360
GTCAAGATCA GGCTTTGAAT GTTGATGAAT AGGAAATAGG CCAGAGACAC AATAAGACTC 420
CCCTTGGCTA GGCCACTAGC AAGGCTGCTT TTATCTTGGC AAAGTCAGTG GCTTGCTTTG 480
GTTTGTTTCT CAAGAATAAA GAAATGTATA ACTAACTGCT GGGGTCCAGG GACATTGTTT 540
TTCCTGTACA GCACATTAGT ATCTTAGTTT CTTCTCTCAG CTTCTTACTG GGTCATTTTT 600
TAAAACCTCA ATGACTTGTG GGTGTAATTC ACCAAGCCTG GCTGGGAAGA AGGGTAGGAC 660
CTGTGCAAGT AAACAAGAGT TTTCAGAGGA GGCCTGCTCT GCCTTAGCAT AGTAGGCCTT 720
TGATATTTCA TGCTTGGATT TTGGCCTTGA CCTTCTACCC CAGCGTCCCC CTGTCCCTGC 780
TGTCTGAGGA GCAGTCCTTC AGTCCTTTTT TTTGAGACAG TCTCGTTCTG CTACCCAGGC 840
TAGAGTGCAG TGGCACAATC TCGGCTCATT GCAACCTCCG CCTCCCGTGT TCAAGCAATT 900
CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA TTACAGGCGT GAGCCACTAC ACCCAGCTAA 960
TTTTTTTGTA TTTTTAGTGG AGACGGGGGT TTTACCATGT TGGCCAGGCT GGTCTCGAAC 1020
TGTTGGCCTC AAGTGATCCA CCTGCCTCGG CCTCCCAAAG TGCTAGGATT ATAGGCGTGA 1080
GCCACCACAC CCGGCCCTGA GCAGTCCATC TAAAACACAA GCCCAACCTG GTTGTTGCCT 1140
TGTTTTAAAG CTTCCTGGGA CTTTCCCATC CCTCTATGGG GGTTGGGGAG GGCAAGCTCT 1200
TCAGCTGGCA ACGAAGCCTT GCGTGTTCTA GTGCCTTCTT GCTTGACCAG TCCCATTTCC 1260
TGCCTCAGTC CACAGCATCA TACTGCATTT AGTTCGGTGA ATCCCCTGTG CATTCTTAAA 1320
CCTTTCCACC TTGCTGGCAA GTCAGTCTAG AATCCCTTTC TCAGCCTCTT GTTTGCTCGT 1380
GGCCTCCAGT TCTGTCTTGA AAATCCTGCT GATAACACCA TCTCTTTGAA GCCTTCACTG 1440
AACTTCCCCT TCCTGACAGA GCTAATTACT CACTACCCTT TTCTGCTTCG GTATCTTGAT 1500
TAGGCTTCCA TTATTACAAG TAGATTATAG TGGGGTAATT ACACATTTAA CCATCTGATC 1560
ACCTACTAGG CCCTGAGATC CATTCATCTT TTTTTTTTTT TTTTTTTTTT TGAGGTGGAG 1620
TATCACTCTG TCACCCAGGC TGGAGTGCAG TGGCACCATC TCAGTTCACT GCAACCTCCA 1680
CCTCCCAGGT TCAAGTGATC CTCCCACCTC AGCAGCTGAG ACTACAGGCA TGTGTCACCA 1740
CGCCCAGCTA ATTTTTTGTA TTTTCAGTAG AGCCTCTTTC CTTGGCTCCC AAATGGTTAC 1800
CTTTTTGCTG TGTCCCCACG TGATTGTCCC TGAGTCTGTG TGTCTGTCCT CTTCTGATAA 1860
AGACACCAGT CCTATTGGAT TAGAGCTCAT CCATATGACC TTGTTTTATC TTAGTCACCT 1920
TTAAAGGCCC TTTCTCCAAA CACAGTCACA TTCTTTCACC ATGTTGGCCA GGCTGATCTC 1980
AAATTCCTGA CCTCGAGTGA TCTATCCGCC TTGGCCTCCT GAAGCGCTGG GATTACAGGC 2040
ATGAGCCACC ATGCCTGGCC CATCCATTTG TCTTTGTATC ACATAGCTCA GTGCCCACAA 2100
TATGCAGGTA CTCAACAAAT AGTGGTCAGA ATCAACGTAC TTGGATTTCT GGGGCCTCGC 2160
AGCCCATGGG AGTGGCAGTG TAAGGGCCCG AGTTAGAGGT GGGCAGCCTC CCTCCTGCCG 2220
CCTCTCCTCA CCATTGCTTT GAGTCCCATT GCTCTCAGCA CAGCTGAGTG TCCTGGTGGC 2280
TGCCATCACT GACCTTTGTC TTTGGTTGCT GTAAACCTTT GAAGTACTAA GGAGTTGGCA 2340
GAATGCAGAT GCAGGCCATC CGCGGAGTTG GCAACGACAT GAGCATGGGC TACTGGGAAC 2400
GAAGCAAGCT TTCTAAGGCT GAGTCACCAT CAAGCCTGGC 2440