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

TagContent
EnhancerAtlas ID
HS105-01051 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr1:19764960-19766680 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12045440chr119765518hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Six3MA0631.1chr1:19765843-19765860AATATGGTATCAATTAT+6.07
Sox3MA0514.1chr1:19766629-19766639CCTTTGTTTT+6.02
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_00361chr1:19758908-19766393Adipose_Nuclei
SE_01199chr1:19764813-19765602Adrenal_Gland
SE_01631chr1:19763072-19765859Aorta
SE_01631chr1:19765884-19767381Aorta
SE_02919chr1:19763288-19766511Bladder
SE_03519chr1:19764939-19765496Brain_Angular_Gyrus
SE_03519chr1:19766063-19766633Brain_Angular_Gyrus
SE_04046chr1:19761365-19766762Brain_Anterior_Caudate
SE_05077chr1:19761658-19766915Brain_Cingulate_Gyrus
SE_05833chr1:19758978-19771689Brain_Hippocampus_Middle
SE_07251chr1:19761522-19766675Brain_Hippocampus_Middle_150
SE_08066chr1:19761310-19766915Brain_Inferior_Temporal_Lobe
SE_09593chr1:19761061-19765333CD14
SE_17553chr1:19764964-19767404CD4p_CD25-_CD45RAp_Naive
SE_18410chr1:19761423-19767274CD4p_CD25-_Il17-_PMAstim_Th
SE_19269chr1:19765031-19766537CD4p_CD25-_Il17p_PMAstim_Th17
SE_22607chr1:19764852-19766515CD8_primiary
SE_25786chr1:19760849-19766711Duodenum_Smooth_Muscle
SE_26537chr1:19758694-19767372Esophagus
SE_28668chr1:19762585-19766007Fetal_Intestine_Large
SE_29645chr1:19762772-19766708Fetal_Muscle
SE_31164chr1:19758811-19766683Fetal_Thymus
SE_31447chr1:19763137-19765805Gastric
SE_31447chr1:19765889-19766635Gastric
SE_41031chr1:19761002-19767422Left_Ventricle
SE_42185chr1:19758942-19767388Lung
SE_44300chr1:19761412-19768336NHDF-Ad
SE_45110chr1:19763704-19765865NHLF
SE_45110chr1:19765868-19766486NHLF
SE_45720chr1:19760211-19770269Osteoblasts
SE_46635chr1:19763027-19765765Ovary
SE_46635chr1:19765887-19766638Ovary
SE_47234chr1:19762903-19786782Panc1
SE_48688chr1:19763147-19766695Right_Atrium
SE_50058chr1:19758801-19767340Sigmoid_Colon
SE_51211chr1:19758996-19767090Skeletal_Muscle
SE_52345chr1:19758916-19766642Small_Intestine
SE_53453chr1:19760224-19765842Spleen
SE_54550chr1:19758998-19766826Stomach_Smooth_Muscle
SE_56083chr1:19760796-19765221u87
SE_56083chr1:19765868-19768296u87
SE_62519chr1:19761354-19815005Tonsil
SE_65446chr1:19764060-19765802Pancreatic_islets
SE_65446chr1:19765879-19766620Pancreatic_islets
SE_67779chr1:19760796-19765221u87
SE_67779chr1:19765868-19768296u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr11976641619766567
chr11976596419766262
Enhancer Sequence
TAAGAAATAA ACTTAAGTAA CCCCATAGCA TGCTGAGTGA AGAGAGGAGC CTTTCTCAAG 60
TGTCTTAGTG CCGAGGAGTG GACCAAGGGG CTCTGAAAAA TGACCAATGA GGCTTCCCGC 120
CACTCAGAGG AAGCCAAGCT CAGAAAGGCC ACGAAGACCA TCCTCGCTTA AGCGCGGGGC 180
CAGATTCCAA GGCCAGGTCT GCTCCGCCTC ATCCATTTCT TGTGCTGCTT CCCAGTGAGA 240
CTCAGCAGAG GACACACGAG GCCACATGAG GTACTCACAT CAGGATCTCA GCTCTCTAAC 300
ACAGGGAGGG GTGCAACGAA GGCAAGGACA CAGGTGCTGT GCGTGACTCC CCACCGGGGC 360
CGGCGGGCAC TGGGTGGCTC AGAGATCATT AGGAACGGTC GCTCCCTCCC TTTCTCCTGG 420
TTTCCCTTCT GTCCTCTGAT AGAGGAAAGT GGCTTAGATC ATTCTCACAG GAAGATTAAA 480
TCCAGAGCAA GGGAAAGGGA TAGGAATCCG TTTCCAATCA ATGATGGAAA CCAGATTCCC 540
TCATCAGTTG GGATTCATTC TTACATGTTG TAAACATCAC AGAGCTCCAC CCATGGCTAC 600
AAGCGTTCAG GAGGTATGAA GCATGGTGGC ACATCCTGGG TGAGAGCTGC CTGTGGCCAA 660
GAAGCCTCCC GGCTTGGGCT GGCCCATCTG AGGGACAGGA AGCAACACGT CTCTTGGAAG 720
TTATCCCCAA AACTCCCATC TCAGAAAGGT GAGATAAAGC ACAAGACTGT CCCACTCTTG 780
TAAATGTTCT ATATTTACAG GAATAAAGTT TTAAAACCAT CTTAGACAAC TATAACCTCC 840
TTCCTGTAGA ACATACCCAT GTACATTTGT ACTCATATGG GAAAATATGG TATCAATTAT 900
TAATAGTAAA GTATTTGAAT TAAAGGTCTT TTGTTCTTGA AGAACCACGG GATCTCAGTT 960
TCAGTGGCCT TGGAGTCCCA CTTCCCCCGT ATGAAATCCC TAAAGCACTA GGTGTTTTGA 1020
CCCCTGCTTG ATCTTGACTA TGGGGAAAAT GCACCATGTC CCCAGTCAGC CTGTGTCACG 1080
CGGTGCTGGC TGTTTGGCAG CTCTGCCTTA CACTGCAGCC TCCAGCACAG AGAGTCCTCT 1140
GTCCAGAACC ACCTCAAGGA TGTGCAAGTT CTCTGCCACA TGGCATCCCT CAGACACCTG 1200
AAGTGAGCCA TCTCAGCCTC CCTCCAAGCA GCTTCCCTCC CGGCTGACAC TCCCAGCTCT 1260
GCTGTGTCCT GCACATGGCA CGCTTCCGAG ACCACTCGCC CTCGGCTGTC CCCTGGGGTT 1320
CATGCCACTG GATCACTGGG TGCTTAATAG GCGCCAACCA TTTCAGAAAC CACCTCTTAT 1380
TCCCGTGAGA GCAACCCCTG CAAGTATTCT GTTTTGGTTT TGTTTGTGCT TTTTCTTTTT 1440
GCAGGAATCA AGGCCCTAAC ATCCAGAACC TCAGCAGTCT CTCTGGCTGC CATCCACATC 1500
ATCTGCCCAG ACACAAAGAG AGCGGGACAG GACCACAGCG TGGCCAGGTG GGGGTGCTAC 1560
CGGTTTTCCC TACAGCTGAC GTAAAATACA TATATTACTG CAAATCTAAT AACCTGCTTA 1620
GAAAGCACTT CAAGGCAGAA CCATTCAGGA AATACCTTAA TACAAAATAC CTTTGTTTTT 1680
CTTTTCTTTT TGTTTTTCTG AAGCAGGGTC TTGCTTGCAT 1720