EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-24539 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr3:129321030-129324060 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr3:129322775-129322786GGAGGGTGTGG-6.32
ZNF263MA0528.1chr3:129321263-129321284TCCTCCTGCTCCTCCGCCCCC-6.85
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00112chr3:129305417-129325570Adipose_Nuclei
SE_00978chr3:129319808-129321592Adrenal_Gland
SE_00978chr3:129321697-129323153Adrenal_Gland
SE_00978chr3:129323570-129325703Adrenal_Gland
SE_01893chr3:129320358-129325457Aorta
SE_04322chr3:129319668-129323752Brain_Anterior_Caudate
SE_05345chr3:129310701-129325499Brain_Cingulate_Gyrus
SE_05951chr3:129308023-129325521Brain_Hippocampus_Middle
SE_07365chr3:129320968-129325546Brain_Hippocampus_Middle_150
SE_08750chr3:129311577-129324158Brain_Inferior_Temporal_Lobe
SE_09767chr3:129321251-129323545CD14
SE_25754chr3:129320148-129325522DND41
SE_26494chr3:129322626-129323696Duodenum_Smooth_Muscle
SE_27065chr3:129320439-129327730Esophagus
SE_29874chr3:129321554-129323225Fetal_Muscle
SE_31569chr3:129320973-129323348Gastric
SE_31569chr3:129323423-129327747Gastric
SE_33524chr3:129321014-129326721H2171
SE_37506chr3:129321224-129323754HSMMtube
SE_37994chr3:129310132-129325566HUVEC
SE_40701chr3:129308079-129325658Left_Ventricle
SE_42115chr3:129307923-129325621Lung
SE_46476chr3:129321099-129324056Osteoblasts
SE_46996chr3:129321102-129321453Ovary
SE_46996chr3:129321736-129322814Ovary
SE_46996chr3:129322871-129323297Ovary
SE_47266chr3:129310010-129324076Panc1
SE_48609chr3:129310376-129325641Right_Atrium
SE_49818chr3:129323622-129325482Right_Ventricle
SE_50249chr3:129319807-129325616Sigmoid_Colon
SE_51354chr3:129310040-129325518Skeletal_Muscle
SE_52687chr3:129320970-129325489Small_Intestine
SE_53375chr3:129320912-129328307Spleen
SE_62855chr3:129293187-129347490Tonsil
SE_65523chr3:129319825-129321411Pancreatic_islets
SE_65523chr3:129321577-129323275Pancreatic_islets
SE_65523chr3:129323511-129324084Pancreatic_islets
SE_68869chr3:129320930-129322808H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr3129322103129322311
Enhancer Sequence
GTGCCTGCTG AGACCACTCC ACTTCTCTGG CTAAAACCCT TCATGGCTCC CAGGACCCCA 60
GGATAAAGTC CAGACTCCCA AGGACGGTCT CCCCAGGCCT CCCTGGCCCT TGTGTCATGT 120
GCTTCCCACT CTACTCGCCT GGCCACGCAG ACCCCCTCGA GCCTGCTCAC AGCCTTCGCA 180
CAGGCTGCTC CCTTTGCCTG GATGCCTTTC CTCTTCTCCG GCCTCACCTG GCTTCCTCCT 240
GCTCCTCCGC CCCCTCCGCT GGGCTCCCTC CACCCTCATT CTCCCTTTGC GGCACGCATT 300
GCCCTGTGTA TAAGGGCCTG GTCACACATC CGTCCTCGGC TCACCTGCCC AGCCCACAAG 360
AGTAGAAACA AAGTGAGTTG CCATTGGCTC CCCAGGGCAC AGCATGGGAC TGGGCTCACA 420
ATAGGGACTT AGTAAATGTC TATGGAGGTG TCATCTGGGG CTAGAAGTAG GAGATGGTGG 480
GGTGTTTACA GCTGCAGAAC AAGCCAGATT AGGCAACTGC TCTCCAGGAC CAAGCAGAGA 540
CCTGTGCTAA TAATGTCCCT TAGAGTAATA ACAAGAAGAA CTGCCATCTG CTTGGTGCTT 600
ACTGTGTACT GGGTACACTG AGCTGCATTT ATCGATTCAT CTAGTCCTTA AAACAATGCT 660
TTGGGATAAG GATTGCTTTT ACTGTCCCCA CTTCACAGAT GAAGAAACTG AGGCCCAGAG 720
AGGTTAAGTT CCTTGGCCAA GGTCACACAG CTGGGAAGTG ACAAAGTGGG ACTTGAACCC 780
AAGCAGCCTG ATGCAAAGTC TAGGTTCTGA ATCTGTCGCT GCATAGCTGG CAACAGCCTG 840
GAGCAAGAAT AATGATCCCT CCCCCACCCC TGCCCATGCT AGAGGCCCAG ACCGGGGACC 900
TTGAGCACCT CTGGGAGATA CTGCCAAGTG GCACTGGCCT GTGCCCACAG CGGGCACGGC 960
GAAGAGGAGA AGGGTGTGGA AAACACAGGG AGGGTGACCA AGGAAGGCCG CAGCCGGAAT 1020
CTGTGGCCTT GGGGTGGGGA AGAGGCCCTT CGCCACTCTG TCCTGGGGCT GTGTCCCTGG 1080
AGAGGCCCTG TCCCCTTAGG TAGAGAAGCT CCAGCCCCCC TCAGCTGGGT GAGTCACTGC 1140
ACCGAGGGAG CGGACCGTGG GAACCAGAAT GGTTCTTGCC AGAGGGGGAG GGAACCCTGG 1200
GCTGGCCTAA GGAATCCCAC AGATCAGCTT ACACCAAAGG GCCGAGACAC AGGGCCTGAA 1260
ACTACTGGAG GAAGGCCCTC AGTCCACAGG ACACTTCTCT CCATTCAGCG ACTCCCCACT 1320
GAGACCCCCA GTGCCAAACA CAGTTGCCTG CGAGATGAAG CTCTGGGGTG GAGATGGTGG 1380
ATGAACCAAC CATGGCACAG GGCAAGCAGC CCCACCACCC TTTGGACTGT CTGCCCTGCT 1440
CACCCACCGT GACCTTTACT TTCAGGGTGG CCGGCCAGAT GGTGGGCAGT CGTGGGAGAC 1500
CGACCTCGAC CTTGGGAGAA GGAATCTGCA TTTTCTCAAA GCCCCAGTGT TGGGCCCGCC 1560
CACAGAGGAA TGGTTAATCT CATGAAATTC TTGTCACAGC CATGGAGAAG GGACAGGGTG 1620
GGGCCCCAAG GAAGGCTTGG GTCACCACAA GAAGGCTGAG TTCTGCATTT TGCTGATGGA 1680
GATGCAGCTT CCTAAGGGAA TGGCAGGCAG TGGAGCTGAA GTGGGCTCGC CAGACTCAGA 1740
TGGGTGGAGG GTGTGGGAAA GGCCCCAGTG TCATTCTGGG GCCTCATTCC TCAGGGTGAA 1800
CTATGGGGAT CAACAGACCC AGCTCCCAAA GCCAGTGTGA GGAGCAATCC CTTGCCATGA 1860
ACTTCCTTTC AGGGAACCAC ACCAAGTCCC CTCCCGCACC CTTGTCATGT CAACACACAT 1920
GCTGATTCCG TCAACCTGGC CCCCCTTGCT ACTGCCCAAC CCAGCCTCAG ACACCTGGGC 1980
CCCATGCCTG CCTGTACTCC TCCTCATTCC CCACTGAGCC CCACGGCCCT CTCCTGCCCC 2040
CAAAACACCC CTGTTCACAT CCCTCCATTC TCCTGGCCCT GGCATCTGCC CACCCCAGCT 2100
GCCTGGGACG CCCCCAAAAC ACACGCACTC TGAGATCCAA GTCCAGAAGG CAGCAAAGGC 2160
TGGGCATTAA AAACACAGAT GCTGAGGCCA GACAGGCTGG ATTCAAATCC ACCTCTGCTA 2220
GTGCCCAACT GTGTGATCCT CAGCAAGTTG CTTAACCTCT CTGTGCCTGT TTCTTCATCT 2280
GTAAAATGTG ATGAGAATAG AGGCTACCTG AGAGGGTTGT TCTGAGAACT GGGAATTGTG 2340
ACATGTGATG CCCCTAGCTG GCACTCCACA AGTGCTATTG TTTACCCCAG ACTCCCACAC 2400
CTGGTACATA CTAGGTGCTC AGGAAATATT TGCAGAATAG GTGAATAAAA GTTGGCCTCA 2460
GGCACACACC TGTTTGCCAA CCATGCAGCC TCCTCAGAGT ACCGACTCAT GCCCAAATAC 2520
CTGCGTCCCC TGCCACGCAC ATCCCACTGC ACACCTAGCC CTGTCCCGTT GTACCAGTGT 2580
CTGTGCAGTA CACCTGTCTG CCCTGTGCGT CTTCAGGCCC CAGCTTGCTG GCACACAAGT 2640
CCATGCAGAC ATCTGCAGGG CCCTGGTGCA CACCTGTGTG CCTCCTTGCA CACCTGCCAC 2700
ACCCATGCAC CCATCACCAA CGTGCAATGG TAACTCTGAC AGGCTCACGC AGTGGCCCCA 2760
GAACACAACT TTGGTCAGGC ATGCAGTCAC TTACTGCGCC CTCAGCATGC ACCTGTGACC 2820
CTCACGTGCA TACCTGGGCT TTATGCGCAC CTGGGTACCT GTGGCAACTT GGACCCCTCC 2880
CAGTACGCCT AGGTATGCGC GCCCATGAGC CGGCACTCAC TTGAGTCCCT GCACATGCCC 2940
ACCTGGGCCA TACAGGCGCC AGTAGTACCC CTCGGGGGAC ACCTGTATTC TCGCGTGCAC 3000
ACCTGGGTTC CACGTACATC TGGATCTCTG 3030