EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS044-00165 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr1:22235750-22238700 
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
CAAAGATGCA CACTTAACAG CCAAGAGAAT ATTAACTAAA GAAATATAAG AAAAACTCAG 60
GCAGGGCAGG CAGATGGAGC CTGGAGTGAG GCAAGCAGAC AGAGAGCACA TGCTGAATCC 120
CAGAGATCTA GGAAAGGGAC AACTCATGTG GCCCTGAGCT TGCCAGCAGC CAATGGGAAG 180
AAGGAAACCT GACCAGTCCC TAGATTCCAT GTCTCACAAT GTAAAAACAA ACCAGTTGCT 240
TAGAAAAAGC ACAACTATCC CTGATACTGA GAGCAGGGAA TGTCCCAAGG GACAGGCTTG 300
TCTGGCACCC TTCTCTGCCT CATCAGTGGG GCTGGCATCC CCTCAGAGTC TGCTGACCAT 360
GACCCTTTGA AGCTGAAGCC AGGGGCAGAG GCTACAGTGA TCAAAGATTC AGGGAGCTGG 420
AATGGCAGTC CAGTCAGTAC CCCACCAACC TCACCCCAGC AGCCTTGGTC TAGGCAGGAT 480
TACCCATCAC TCCCCAAACC CGAACACAGC CAGTGCCCAA AATAGCTAGA GCAGGAGAGG 540
GTGCCAAGAG GCCCTGGCAA GGGCCTGGGC TAGGCCCACC TACAGGAGGG CCCAGTGGGC 600
CAATGCACAC ATACCTCTGG TGCACAAAGA GGCACCTTCA GTCAGGCACA GAGCCGTCCC 660
TGGGAGTCCC CCACCCACCA GGCTCCCCCC TCAGCTGCAC GTTGCTCACG CAGAACTTGA 720
GCTGCTGCTC CACCCTTCCC ACAAAGCAGG CCTTCCTGCC TGAGCCAGAC TAGAAAAGCC 780
TTCCACAGAA ATGCCACCGC ACCATATAGG GAAGTGCCTG AAGACCTCCC CGCCCCACCT 840
CCAGAATCTG CCAGAATCAG CCCCCTCAGG ATCCTCCATG GCGATGTTGG TTCCTCCCTG 900
GGTCCCCCAG CTGCAGACCA ACACAATGGG GGCTATTCTG GGCTGCACGG GGTATTTAAA 960
GCTCTGACTG GGCCTCCTCC CTGGGGAACA AAAGGCCTTG CCCTCCGTAA GACCTTCCTG 1020
AAATTGTTCC TGCCCAGACT GTGGTGGCTG CATCCTGTAC TGTTCCCCAC CTCCCCTGCC 1080
AGGCCCTGAG GCCCTGTAAG ATTCAGCACA AAATGCCTCC TCCAGGAAGC CCACAGGGCT 1140
GCCTCCTGTG CTCAGCAGCA CTGCCTGAGA CCCTCAGAAA AGCTGGGTCC TGGCTCAACT 1200
CTGCCATCGA TCTTCTCTGG GTCCCAGTTT TCTCATCTGC AAAATATGGA TGTGAATCCC 1260
AGTGTGTGAA AGCACTCCAG AGGCTTCCAT GGTTAGGATG AGTAGTGTCT CTCCAGCCAC 1320
TTTGTGAAGC AGAATATAAG CAGGAACGGG AATTGGTCTG TTTTGTCGCT GCCCTTTTTC 1380
TAGCACCTGG CACACAGTAG GTGCCAAATA AATATTTACT GACTGATACA AATATTTAAA 1440
GAATGTGTCT GTAGCCTCCA TAGAACCACC CAGAATGCCA GGCACACAGG TGGTTAATAC 1500
CCTCGATGGT AACGTTGCCA GCTCTCAGCT TGAGCACAAA GAACACATCA AGCCTTATGC 1560
TAAGTACCTG ATGTTAATTA TCTGATTTAA TTTGCTCAAC AGTCCCAAGA GGTCGGTACC 1620
ATTATCTTAT TTCACAAGCA AGAAAACGGG AGTTCCAGTC CAGGTGGTTA AGCAGCTCGC 1680
CTGAGGTCGC AAATGGCCAA GCTGGGAGTC AAGCCCAGGA GCCCTGAAGC CCCTGGCATC 1740
CTGCGCCAAA TGCACATTGA AGAAAGGCAG TCGGAGAGCA CTGGGTGGGG AGCCAGGAGC 1800
CTGAAGTCAG CCACTAAGCT GTGTGACTTC AAGCAAGTTG CTTGGCCTCT CTGAATCAGT 1860
TTTCTCTTCC ATAAAAACAA GGGCATGAAT TCCTCTTCTT CAGGTCGTTG GTAGGATCAA 1920
AGGAACCAAA GATGTGACTC TGTCTCCCAC ACTAGCCCCA GCCCCTCCCC AAGGGCAGCA 1980
GCTGTGAAGG ATGGTGGGAA GATGTACTGG GAGGAGGGGG CTACCCAGAG CTGGCCCCAG 2040
AACAAAGCTC CACAGCTGCT GACAACAGCT GGGGAGAGCT CTGGGCCTGG CCCAAGCAGG 2100
GGGAGAATGG GCAGGCTGGG AAGTCACCTC TGGCCCTCCT CTGTCACCCT TCCCTGCTGA 2160
CAGCTGCTGA GGCCTCAGGG CCAAGGGCCC CAGAGCAGGC AGGGAGTGGG GGTGTGGAGG 2220
GGGTGGGCGG GCTGGCTGGG GTCATCTTAG TCCTCATGCT GTCAACTGCT CAAGCCTCAG 2280
GGTGCCTGGC CTCGCTGTCC CATAGCACAG CCCTTTACCC AGTTCCCTGG GAAGCCTGGG 2340
TGGAGAGGCC GGAGCAAAGG TCTGGGGCTG AACATGCCTT AACTGGAGCC TGGCCTGCTC 2400
CAGGGCCCCC GTGGGGAGGT GCAGGGCCGG GAGGGAGGGA GTCCTGAAGA GGCTTGCAAT 2460
TTCCCTGGTG CACAGCCCCA CTGCAGGCCC TTCAGGAAAC GTCCCTGGAG GCTGTGAGCT 2520
TGGCCCACCC CAGCCCATCT CAGCCCCCTC AGCTGCCGGC CAGCCCAGCT CCACTCCCAG 2580
TTCGGTGCCA AGCCTTTCCA GCCCGCTCCA GCCCACGCAG CTCTCTCTCC TCTGAACTCT 2640
CACATACCCA TAATTACAAC TGACCATATT TTCCAAAGCA GAAATCAAGA AACCACTAAA 2700
TAAAGGATTT CTGGGCTACT TCTGAGTGTC AGAGGCAGCC TGGGAGGTGA AGTTTGGATG 2760
CAGAGGTATT CAAATCTCTG AGACACGTTG ATAGTTTTTT GCGATGACTA CTATATCTAT 2820
CATATTTTAT TAATAAGTCA AAGCCATCCT AGGAAATGTG TGTTGGGCAC ATGCCACCCC 2880
ATACCACTGT TAACTGTTGA CTGGACACTT TAGCCTGGCA GTTTCCTAGC TGTGTGGCCC 2940
TGGGCAAATC 2950