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

TagContent
EnhancerAtlas ID
HS182-05416 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr12:113683330-113685790 
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: 38             
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_09132chr12:113684557-113684823Brain_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
GGGAGGCGGA GCTTGCAGTG AGCCGAGATC GCGCCACTGC ACTCCAGCCT GGGCGACAGA 60
GCAAGACTCC GTCTCAAAAA AAAAAAAAAA AAAAAAGAAA AGAAAAGGGG TAGGCCCCTC 120
AGTATCACCC TTCCTGAGAA CAGTCATTCT CTGCTTTTTC TGATCAGAGC TCCCTCCCAG 180
GAGGGGCCCT TTTATCCAAA GCGATCTCTG GCCCAGGCAC CAAAGAAAGG CCCCAGTGGT 240
TTACGCAGCC GGGCTGCCCC CTGCGCCTGC TGGGTGAGGG GTGGGTCGTG GAAGCCTTCC 300
CCTCCTGCCT GTTCTTTCCT GCTCCTCCCC AGTGCATCTT TATAGCTGGC ATATGGAAAC 360
TGTTTCTATT TATCTGGCAC CACCAGGACG CTGCTGCATG CTGTGCTCCA GCAAACAGAA 420
ACCTTGGATT CCCTGCAGGG TCATTTCCGA TGTGGCGTGC AAAGCAGCCA GCTGTTTCGA 480
GGGAGCGTCT GGGCCCTGTG ACATCAGCAT GTGGGAGTGT TACCGTGTGT GCAAACAGGT 540
CATTCTGGTT TGTCTGCCTG TCCTCTGCAC CGGGATGTCT CTCCTGCTTC GAGTCAGAGT 600
TTGCGTTGTT GTTTTGTATT CTCATGCCTG TCAGTTCAGC TGTTTCTTTC CACTCCTTCC 660
CGTCCTCTGA GTGGTTTTAC GTTCTCTCCT CCGGGCTGAT TGCCAGGATT CAGGGAGGGA 720
GGTTAAGGGG CTGGTGCCAC ATAAATCTTT AGTGGCCAAA GTCTGCAGGC CTGCAAGGCT 780
GCGCCTGTCC TCTTGGTCTG GTTTTCCCAA GAGAGCTGTC TGCCCAGGGC ACCAGAAGGG 840
CAGGACAAAA TGTTTCCCTT CGTGGAACTT TCCCCAGAGG CCCAGAACAG AGATGCAGAA 900
TACAGTCTTC CTGGTTGCCA AGAGTGTTCC TGGTCAGCCT CCTCTGGTCC TTTCTGAAAC 960
CTGCATGTGG AGCTTGCTGG CTGTGGGAGC CAGGGAGACT GCAAATCCTG CCCGCCTGCC 1020
CACGCTGCTG CTCATCTCCC TCCCTCCTAT GTCCGGCCCG GTTGCCTCCC AGGAAAGGTA 1080
AACATGCAGA GGCAAGGGCT AGCTGCCGGC CTTCTGGAGG AGGCAGTGGA GGGCCAGCTT 1140
CCTGACAGCC CCGTGGTGAG GTCGTCCTGT CTTCTCAAGC TGGGCCCCTG CGACGTGCCC 1200
CAGTTCCTGC CTTTCCAGCT GGCCTGGAAG AACCCGTTCT GCTCTGGGCA AGAACAGTGC 1260
CAAGGTCAGA GGCCAAAGGT GTTGCTTCTT CCGTGGTCCG TAATGAGCAC CAGTTGGAGA 1320
GGGCCAGCCC CGGCACACAG AGGAAGGGGC TGGACTGGGG TGATGCGGGG TGAGCCTGCC 1380
CGGTCACTTT GTTGGCTAGG ATGCTTCCTG TGCTTTCTGT GCCTGGTACT CCAAAGATGC 1440
GAGTGCCAGT CATTGACCTG GAGGTTCTGC CCAGGGTCTG TGGGCAGTAG GAGGTCAGAA 1500
CAAGGCACCA GGCCACTAGA GCAGGTGGGT GTAAACAACT GTTGGCATTC GAGGCTGCCC 1560
AGGTAGAGGT CCTGGAGTGA ACCCAGTGGG CACGATGGGC TTCAGTGGGG CAGAGTGTCC 1620
TCTAGCTTCA CACACAGTGC TGATGACTCA GGCCAGCTGG GGGCCCCTGC ACATGCTCTT 1680
AGTTCCCACG TGGAGGGTAT TCATTTTGAG GAAGCTGGGC CTGCCGGGAT TGGTTCCCCA 1740
GCAAGCAGGG GCTCATTCTC CCAGAAACCA CTCCATCTGC ACTCACACCC TGACTCACCA 1800
GGCTCACATC CTGACTTACC AGGACTTGGC TATCAGCCTG TCCCCTTTGA TCTGCCCCTT 1860
CTGCCCCCTG CCTTCCCGCT TTCTGGGCCT GAAATGTCCT CCTCAGAAAG CTGCCGAGCC 1920
TTCGAGCATA CCTTCTGCGG GAACAACGCA GCACTCGGAG TGGGAGCATA TCCATTGTCC 1980
CTTCAGCCAC TTCTGCAACC TCTTAAGTGG GGAAGAGGGT TAGACAGCAG ACAGGGCAGG 2040
GGATTAGCAC TCCACGAGGT GGCCCAGCCC CACCCGGCCC CTGCCGTGCC CTCGTCTTGG 2100
CTGGTACAGC TGCACTGCTG CGTGAAGGCC ACGTACAAAA GGAACAGAAT GGAACTGTGG 2160
CTCCTCGCCT TCCATTTGCA CCCTTTCTAT AATCCCTAAA TATGTAGCCC AGTTGCTCGT 2220
GCCTTGATGT GAAGGAGGCC CTTTGCGATC ACCTGTGGCT TTCTTGAAAA GTCCCTGAGT 2280
GGCCAGTGTC ACCCCAGGCC TTCCATCCCT CTCTCCGTGT GGAGAAATGA GCGATCATGC 2340
TTTGCCTTTT GGGACCACAT GAGCACTCCA AGTCCTGTTT TCTGAGGTTG AGTGGTTAGA 2400
AGCACAGAAC AAAGTCCGTC CTGGGAGGGG GAGAATTCGC TGTTCTTTCA CCTTAGCTCT 2460