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

TagContent
EnhancerAtlas ID
HS039-00141 
Organism
Homo sapiens 
Tissue/cell
ESC_NPC 
Coordinate
chr1:22235800-22238500 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2445130chr122237722hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MyogMA0500.1chr1:22237908-22237919GACAGCTGCTG+6.14
Tcf12MA0521.1chr1:22237908-22237919GACAGCTGCTG+6.02
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00032chr1:22219419-22267496Adipose_Nuclei
SE_00908chr1:22235514-22242299Adrenal_Gland
SE_01556chr1:22235059-22242385Aorta
SE_02999chr1:22235920-22237166Bladder
SE_02999chr1:22237345-22237955Bladder
SE_02999chr1:22237999-22239189Bladder
SE_06476chr1:22235474-22238889Brain_Hippocampus_Middle
SE_13865chr1:22227437-22237425CD34_Primary_RO01536
SE_13865chr1:22237959-22239034CD34_Primary_RO01536
SE_23160chr1:22237333-22238567Colon_Crypt_1
SE_23793chr1:22237648-22238327Colon_Crypt_2
SE_24796chr1:22237541-22238537Colon_Crypt_3
SE_25801chr1:22235294-22242489Duodenum_Smooth_Muscle
SE_26605chr1:22235509-22242357Esophagus
SE_28012chr1:22235488-22242414Fetal_Intestine
SE_28954chr1:22235552-22242440Fetal_Intestine_Large
SE_29681chr1:22234910-22242400Fetal_Muscle
SE_36920chr1:22219607-22267740HSMMtube
SE_37945chr1:22220303-22255266HUVEC
SE_39947chr1:22234842-22236953K562
SE_40620chr1:22234922-22242399Left_Ventricle
SE_42167chr1:22234999-22242386Lung
SE_44366chr1:22235089-22239328NHDF-Ad
SE_45173chr1:22235732-22237092NHLF
SE_45173chr1:22238204-22238804NHLF
SE_45699chr1:22234847-22242422Osteoblasts
SE_46764chr1:22235798-22237204Ovary
SE_46764chr1:22237309-22239252Ovary
SE_47433chr1:22235733-22240874Panc1
SE_47860chr1:22236045-22236448Pancreas
SE_48478chr1:22235486-22242245Psoas_Muscle
SE_48565chr1:22235175-22242369Right_Atrium
SE_49456chr1:22235561-22237122Right_Ventricle
SE_49456chr1:22237167-22238544Right_Ventricle
SE_50206chr1:22235495-22242384Sigmoid_Colon
SE_51733chr1:22235366-22239269Skeletal_Muscle_Myoblast
SE_52462chr1:22235524-22239350Small_Intestine
SE_53700chr1:22235033-22242399Spleen
SE_54522chr1:22234975-22242507Stomach_Smooth_Muscle
SE_63519chr1:22235220-22240758HSMM
SE_68865chr1:22235783-22238487H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12223583622236001
Number: 1             
IDChromosomeStartEnd
GH01I021893chr12222048622243088
Enhancer Sequence
AAAAACTCAG GCAGGGCAGG CAGATGGAGC CTGGAGTGAG GCAAGCAGAC AGAGAGCACA 60
TGCTGAATCC CAGAGATCTA GGAAAGGGAC AACTCATGTG GCCCTGAGCT TGCCAGCAGC 120
CAATGGGAAG AAGGAAACCT GACCAGTCCC TAGATTCCAT GTCTCACAAT GTAAAAACAA 180
ACCAGTTGCT TAGAAAAAGC ACAACTATCC CTGATACTGA GAGCAGGGAA TGTCCCAAGG 240
GACAGGCTTG TCTGGCACCC TTCTCTGCCT CATCAGTGGG GCTGGCATCC CCTCAGAGTC 300
TGCTGACCAT GACCCTTTGA AGCTGAAGCC AGGGGCAGAG GCTACAGTGA TCAAAGATTC 360
AGGGAGCTGG AATGGCAGTC CAGTCAGTAC CCCACCAACC TCACCCCAGC AGCCTTGGTC 420
TAGGCAGGAT TACCCATCAC TCCCCAAACC CGAACACAGC CAGTGCCCAA AATAGCTAGA 480
GCAGGAGAGG GTGCCAAGAG GCCCTGGCAA GGGCCTGGGC TAGGCCCACC TACAGGAGGG 540
CCCAGTGGGC CAATGCACAC ATACCTCTGG TGCACAAAGA GGCACCTTCA GTCAGGCACA 600
GAGCCGTCCC TGGGAGTCCC CCACCCACCA GGCTCCCCCC TCAGCTGCAC GTTGCTCACG 660
CAGAACTTGA GCTGCTGCTC CACCCTTCCC ACAAAGCAGG CCTTCCTGCC TGAGCCAGAC 720
TAGAAAAGCC TTCCACAGAA ATGCCACCGC ACCATATAGG GAAGTGCCTG AAGACCTCCC 780
CGCCCCACCT CCAGAATCTG CCAGAATCAG CCCCCTCAGG ATCCTCCATG GCGATGTTGG 840
TTCCTCCCTG GGTCCCCCAG CTGCAGACCA ACACAATGGG GGCTATTCTG GGCTGCACGG 900
GGTATTTAAA GCTCTGACTG GGCCTCCTCC CTGGGGAACA AAAGGCCTTG CCCTCCGTAA 960
GACCTTCCTG AAATTGTTCC TGCCCAGACT GTGGTGGCTG CATCCTGTAC TGTTCCCCAC 1020
CTCCCCTGCC AGGCCCTGAG GCCCTGTAAG ATTCAGCACA AAATGCCTCC TCCAGGAAGC 1080
CCACAGGGCT GCCTCCTGTG CTCAGCAGCA CTGCCTGAGA CCCTCAGAAA AGCTGGGTCC 1140
TGGCTCAACT CTGCCATCGA TCTTCTCTGG GTCCCAGTTT TCTCATCTGC AAAATATGGA 1200
TGTGAATCCC AGTGTGTGAA AGCACTCCAG AGGCTTCCAT GGTTAGGATG AGTAGTGTCT 1260
CTCCAGCCAC TTTGTGAAGC AGAATATAAG CAGGAACGGG AATTGGTCTG TTTTGTCGCT 1320
GCCCTTTTTC TAGCACCTGG CACACAGTAG GTGCCAAATA AATATTTACT GACTGATACA 1380
AATATTTAAA GAATGTGTCT GTAGCCTCCA TAGAACCACC CAGAATGCCA GGCACACAGG 1440
TGGTTAATAC CCTCGATGGT AACGTTGCCA GCTCTCAGCT TGAGCACAAA GAACACATCA 1500
AGCCTTATGC TAAGTACCTG ATGTTAATTA TCTGATTTAA TTTGCTCAAC AGTCCCAAGA 1560
GGTCGGTACC ATTATCTTAT TTCACAAGCA AGAAAACGGG AGTTCCAGTC CAGGTGGTTA 1620
AGCAGCTCGC CTGAGGTCGC AAATGGCCAA GCTGGGAGTC AAGCCCAGGA GCCCTGAAGC 1680
CCCTGGCATC CTGCGCCAAA TGCACATTGA AGAAAGGCAG TCGGAGAGCA CTGGGTGGGG 1740
AGCCAGGAGC CTGAAGTCAG CCACTAAGCT GTGTGACTTC AAGCAAGTTG CTTGGCCTCT 1800
CTGAATCAGT TTTCTCTTCC ATAAAAACAA GGGCATGAAT TCCTCTTCTT CAGGTCGTTG 1860
GTAGGATCAA AGGAACCAAA GATGTGACTC TGTCTCCCAC ACTAGCCCCA GCCCCTCCCC 1920
AAGGGCAGCA GCTGTGAAGG ATGGTGGGAA GATGTACTGG GAGGAGGGGG CTACCCAGAG 1980
CTGGCCCCAG AACAAAGCTC CACAGCTGCT GACAACAGCT GGGGAGAGCT CTGGGCCTGG 2040
CCCAAGCAGG GGGAGAATGG GCAGGCTGGG AAGTCACCTC TGGCCCTCCT CTGTCACCCT 2100
TCCCTGCTGA CAGCTGCTGA GGCCTCAGGG CCAAGGGCCC CAGAGCAGGC AGGGAGTGGG 2160
GGTGTGGAGG GGGTGGGCGG GCTGGCTGGG GTCATCTTAG TCCTCATGCT GTCAACTGCT 2220
CAAGCCTCAG GGTGCCTGGC CTCGCTGTCC CATAGCACAG CCCTTTACCC AGTTCCCTGG 2280
GAAGCCTGGG TGGAGAGGCC GGAGCAAAGG TCTGGGGCTG AACATGCCTT AACTGGAGCC 2340
TGGCCTGCTC CAGGGCCCCC GTGGGGAGGT GCAGGGCCGG GAGGGAGGGA GTCCTGAAGA 2400
GGCTTGCAAT TTCCCTGGTG CACAGCCCCA CTGCAGGCCC TTCAGGAAAC GTCCCTGGAG 2460
GCTGTGAGCT TGGCCCACCC CAGCCCATCT CAGCCCCCTC AGCTGCCGGC CAGCCCAGCT 2520
CCACTCCCAG TTCGGTGCCA AGCCTTTCCA GCCCGCTCCA GCCCACGCAG CTCTCTCTCC 2580
TCTGAACTCT CACATACCCA TAATTACAAC TGACCATATT TTCCAAAGCA GAAATCAAGA 2640
AACCACTAAA TAAAGGATTT CTGGGCTACT TCTGAGTGTC AGAGGCAGCC TGGGAGGTGA 2700