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

TagContent
EnhancerAtlas ID
HS044-03536 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr12:113683300-113685980 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GSCMA0648.1chr12:113685368-113685378GGGGATTAGC-6.02
NR2C2MA0504.1chr12:113684590-113684605CAAGGTCAGAGGCCA+6.24
Stat6MA0520.1chr12:113683457-113683472CCCTTCCTGAGAACA+6.01
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00883chr12:113683342-113686698Adrenal_Gland
SE_01635chr12:113683327-113688666Aorta
SE_03074chr12:113683375-113685473Bladder
SE_03506chr12:113684410-113685192Brain_Angular_Gyrus
SE_04226chr12:113683249-113686805Brain_Anterior_Caudate
SE_05290chr12:113676945-113688044Brain_Cingulate_Gyrus
SE_06123chr12:113676787-113688773Brain_Hippocampus_Middle
SE_07164chr12:113681229-113687363Brain_Hippocampus_Middle_150
SE_08283chr12:113683213-113686051Brain_Inferior_Temporal_Lobe
SE_09132chr12:113683621-113684005Brain_Mid_Frontal_Lobe
SE_23178chr12:113683354-113685924Colon_Crypt_1
SE_24018chr12:113683410-113685761Colon_Crypt_2
SE_26345chr12:113681599-113685097Duodenum_Smooth_Muscle
SE_26677chr12:113683335-113686993Esophagus
SE_27860chr12:113683294-113686963Fetal_Intestine
SE_28798chr12:113681446-113686701Fetal_Intestine_Large
SE_29890chr12:113683290-113685679Fetal_Muscle
SE_37095chr12:113677131-113685805HSMMtube
SE_40725chr12:113683293-113688763Left_Ventricle
SE_41860chr12:113683440-113685760LNCaP
SE_42290chr12:113683300-113687155Lung
SE_44290chr12:113683293-113685251NHDF-Ad
SE_46894chr12:113683424-113685786Ovary
SE_47597chr12:113683411-113685798Pancreas
SE_48084chr12:113673313-113688344Psoas_Muscle
SE_48792chr12:113683328-113687025Right_Atrium
SE_49644chr12:113683419-113685464Right_Ventricle
SE_50157chr12:113683349-113685797Sigmoid_Colon
SE_51183chr12:113681221-113686478Skeletal_Muscle
SE_52527chr12:113683325-113686155Small_Intestine
SE_53751chr12:113683299-113685810Spleen
SE_57125chr12:113683422-113683782VACO_400
SE_57125chr12:113683897-113685375VACO_400
SE_57981chr12:113683423-113683883VACO_9m
SE_57981chr12:113683893-113685652VACO_9m
SE_64197chr12:113683297-113685238HSMM
SE_65505chr12:113677296-113687345Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12113683425113685477
Number: 1             
IDChromosomeStartEnd
GH12I113235chr12113673514113686887
Enhancer Sequence
GAGGCTGAGG CAGGAGAATG GCGTGAGCCC GGGAGGCGGA GCTTGCAGTG AGCCGAGATC 60
GCGCCACTGC ACTCCAGCCT GGGCGACAGA GCAAGACTCC GTCTCAAAAA AAAAAAAAAA 120
AAAAAAGAAA AGAAAAGGGG TAGGCCCCTC AGTATCACCC TTCCTGAGAA CAGTCATTCT 180
CTGCTTTTTC TGATCAGAGC TCCCTCCCAG GAGGGGCCCT TTTATCCAAA GCGATCTCTG 240
GCCCAGGCAC CAAAGAAAGG CCCCAGTGGT TTACGCAGCC GGGCTGCCCC CTGCGCCTGC 300
TGGGTGAGGG GTGGGTCGTG GAAGCCTTCC CCTCCTGCCT GTTCTTTCCT GCTCCTCCCC 360
AGTGCATCTT TATAGCTGGC ATATGGAAAC TGTTTCTATT TATCTGGCAC CACCAGGACG 420
CTGCTGCATG CTGTGCTCCA GCAAACAGAA ACCTTGGATT CCCTGCAGGG TCATTTCCGA 480
TGTGGCGTGC AAAGCAGCCA GCTGTTTCGA GGGAGCGTCT GGGCCCTGTG ACATCAGCAT 540
GTGGGAGTGT TACCGTGTGT GCAAACAGGT CATTCTGGTT TGTCTGCCTG TCCTCTGCAC 600
CGGGATGTCT CTCCTGCTTC GAGTCAGAGT TTGCGTTGTT GTTTTGTATT CTCATGCCTG 660
TCAGTTCAGC TGTTTCTTTC CACTCCTTCC CGTCCTCTGA GTGGTTTTAC GTTCTCTCCT 720
CCGGGCTGAT TGCCAGGATT CAGGGAGGGA GGTTAAGGGG CTGGTGCCAC ATAAATCTTT 780
AGTGGCCAAA GTCTGCAGGC CTGCAAGGCT GCGCCTGTCC TCTTGGTCTG GTTTTCCCAA 840
GAGAGCTGTC TGCCCAGGGC ACCAGAAGGG CAGGACAAAA TGTTTCCCTT CGTGGAACTT 900
TCCCCAGAGG CCCAGAACAG AGATGCAGAA TACAGTCTTC CTGGTTGCCA AGAGTGTTCC 960
TGGTCAGCCT CCTCTGGTCC TTTCTGAAAC CTGCATGTGG AGCTTGCTGG CTGTGGGAGC 1020
CAGGGAGACT GCAAATCCTG CCCGCCTGCC CACGCTGCTG CTCATCTCCC TCCCTCCTAT 1080
GTCCGGCCCG GTTGCCTCCC AGGAAAGGTA AACATGCAGA GGCAAGGGCT AGCTGCCGGC 1140
CTTCTGGAGG AGGCAGTGGA GGGCCAGCTT CCTGACAGCC CCGTGGTGAG GTCGTCCTGT 1200
CTTCTCAAGC TGGGCCCCTG CGACGTGCCC CAGTTCCTGC CTTTCCAGCT GGCCTGGAAG 1260
AACCCGTTCT GCTCTGGGCA AGAACAGTGC CAAGGTCAGA GGCCAAAGGT GTTGCTTCTT 1320
CCGTGGTCCG TAATGAGCAC CAGTTGGAGA GGGCCAGCCC CGGCACACAG AGGAAGGGGC 1380
TGGACTGGGG TGATGCGGGG TGAGCCTGCC CGGTCACTTT GTTGGCTAGG ATGCTTCCTG 1440
TGCTTTCTGT GCCTGGTACT CCAAAGATGC GAGTGCCAGT CATTGACCTG GAGGTTCTGC 1500
CCAGGGTCTG TGGGCAGTAG GAGGTCAGAA CAAGGCACCA GGCCACTAGA GCAGGTGGGT 1560
GTAAACAACT GTTGGCATTC GAGGCTGCCC AGGTAGAGGT CCTGGAGTGA ACCCAGTGGG 1620
CACGATGGGC TTCAGTGGGG CAGAGTGTCC TCTAGCTTCA CACACAGTGC TGATGACTCA 1680
GGCCAGCTGG GGGCCCCTGC ACATGCTCTT AGTTCCCACG TGGAGGGTAT TCATTTTGAG 1740
GAAGCTGGGC CTGCCGGGAT TGGTTCCCCA GCAAGCAGGG GCTCATTCTC CCAGAAACCA 1800
CTCCATCTGC ACTCACACCC TGACTCACCA GGCTCACATC CTGACTTACC AGGACTTGGC 1860
TATCAGCCTG TCCCCTTTGA TCTGCCCCTT CTGCCCCCTG CCTTCCCGCT TTCTGGGCCT 1920
GAAATGTCCT CCTCAGAAAG CTGCCGAGCC TTCGAGCATA CCTTCTGCGG GAACAACGCA 1980
GCACTCGGAG TGGGAGCATA TCCATTGTCC CTTCAGCCAC TTCTGCAACC TCTTAAGTGG 2040
GGAAGAGGGT TAGACAGCAG ACAGGGCAGG GGATTAGCAC TCCACGAGGT GGCCCAGCCC 2100
CACCCGGCCC CTGCCGTGCC CTCGTCTTGG CTGGTACAGC TGCACTGCTG CGTGAAGGCC 2160
ACGTACAAAA GGAACAGAAT GGAACTGTGG CTCCTCGCCT TCCATTTGCA CCCTTTCTAT 2220
AATCCCTAAA TATGTAGCCC AGTTGCTCGT GCCTTGATGT GAAGGAGGCC CTTTGCGATC 2280
ACCTGTGGCT TTCTTGAAAA GTCCCTGAGT GGCCAGTGTC ACCCCAGGCC TTCCATCCCT 2340
CTCTCCGTGT GGAGAAATGA GCGATCATGC TTTGCCTTTT GGGACCACAT GAGCACTCCA 2400
AGTCCTGTTT TCTGAGGTTG AGTGGTTAGA AGCACAGAAC AAAGTCCGTC CTGGGAGGGG 2460
GAGAATTCGC TGTTCTTTCA CCTTAGCTCT TGAGTCTTAT TCTCCCCTTT CCCTTTCAAG 2520
GTTCTACCCT GAATTACTCT TAACACAAAA CAGCCCCTCT TCCGCAGATC CTTAAAAGAA 2580
AGGTTTTTAC AAATACAAAC TTACCACATC ACACCCCTTC CTAACACCCT TTGGCGCTGC 2640
CCACTGCACC CCGGGTGGAG CCCGCCCTCT TGCCCGAGGC 2680