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

TagContent
EnhancerAtlas ID
HS176-03788 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr1:223892610-223895120 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata4MA0482.1chr1:223894355-223894366AGGAGATAAGA-6.14
Nr2f6(var.2)MA0728.1chr1:223894565-223894580GAGGTCAGGAGTTCA+6.22
SP2MA0516.2chr1:223893170-223893187ATGTGGGAGGGACTTAG-6.73
ZNF263MA0528.1chr1:223894171-223894192GAAAGAGGGAGGGGAAGAAAA+6.35
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00224chr1:223891886-223912166Adipose_Nuclei
SE_01908chr1:223891964-223894610Aorta
SE_02306chr1:223892116-223896302Astrocytes
SE_04026chr1:223892317-223894515Brain_Anterior_Caudate
SE_05972chr1:223891995-223895701Brain_Hippocampus_Middle
SE_07996chr1:223892580-223894588Brain_Inferior_Temporal_Lobe
SE_23408chr1:223892519-223892911Colon_Crypt_1
SE_23408chr1:223893759-223896170Colon_Crypt_1
SE_25230chr1:223894802-223895832Colon_Crypt_3
SE_26209chr1:223892263-223896172Duodenum_Smooth_Muscle
SE_26925chr1:223892455-223896502Esophagus
SE_31491chr1:223892450-223896280Gastric
SE_33950chr1:223892039-223897144HCC1954
SE_34545chr1:223893587-223897272HCT-116
SE_34979chr1:223893945-223896369HeLa
SE_36294chr1:223892209-223896197HMEC
SE_37129chr1:223886879-223896561HSMMtube
SE_38254chr1:223892197-223897487HUVEC
SE_38957chr1:223892076-223894679IMR90
SE_38957chr1:223894705-223896262IMR90
SE_41495chr1:223892178-223896347Left_Ventricle
SE_42269chr1:223892060-223896221Lung
SE_44530chr1:223892152-223896327NHDF-Ad
SE_44904chr1:223892205-223896189NHLF
SE_45872chr1:223889824-223896323Osteoblasts
SE_49408chr1:223892167-223893562Right_Atrium
SE_49408chr1:223893604-223894625Right_Atrium
SE_50365chr1:223893595-223896281Sigmoid_Colon
SE_51879chr1:223892369-223896155Skeletal_Muscle_Myoblast
SE_53249chr1:223893884-223894596Small_Intestine
SE_53249chr1:223894745-223896091Small_Intestine
SE_55958chr1:223886755-223897239u87
SE_63671chr1:223892313-223896169HSMM
SE_64794chr1:223894664-223896174NHEK
SE_65644chr1:223892460-223893201Pancreatic_islets
SE_65644chr1:223893499-223896161Pancreatic_islets
SE_67677chr1:223886755-223897239u87
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1223892629223893260
chr1223893295223893662
Number: 1             
IDChromosomeStartEnd
GH01I223704chr1223892008223897501
Enhancer Sequence
TGACTGTCAT ATGTCACAGC AGGATGGGTA GTTGGCTGCC CCCAGCCCCC TCCTGCCGCT 60
CCCTGTTCCA GCACCCTGGC CCACCAGCCC CTTCCTGGCA ACTCCCATAC TCCCCCAGTT 120
CATCCACTAA AGGATTAATA GCTCACTCAG GGGAGGCTTC CTGCCCCTCG GCCAACACCA 180
ACTTCCCTTT CAGCAAGCCA GTGTCGGCAC TACAGTGGTT TGGAATACTT TCAATATCAC 240
TCCCTGTTAA CAAGCCTATC CTTGGACTGG CTGAGAAAAG AAATGGAACG GGGCAAAGTA 300
ACAAAACAAA GAGGCAAGAC AGAGCCAAAT GTCTCCTATG GTTACCTAAA TCACAATTTA 360
GACAAGCACT GGTGATTCTT GCACATAGAG AACCACCACT GAACTGTACA GGGGAAACTG 420
GTTTCTGCCC CAGAGATGTG TTGGGGAAAT GACATACTGA CCACCATGAC TACATCCTCG 480
GAAGACTGAG TGGCAGAGTG CTACTTTGGC TTTCTTACCA GGTGAACTTG AGCATATATC 540
TGGGCAGTTC TAGAATTTCG ATGTGGGAGG GACTTAGGGA TGAAAAAAAT AAAATGTGGA 600
TGGTAGATGG CATTTGGGGC AGGGGATTGG AGGCTTGTCT TGTAGCTGTT TCTGCTTAGT 660
AAGCTCCCTG TTCTGGCTTA GAGACATATT TATTGGGGAG CTTGCTGATG GGAATTATGG 720
ACGGGGCCAA CTCCTCTCCC AGCACCCTGT GGTGCTGACA TCTGAGGTGA TCACTTCCCA 780
TGGAGTGGAG AAAAGCATGC TGCTCTATAT TTGTTCCCTA CAACAGGAAG CGTGAAAACA 840
GGATTTGCTG CCACATGTCA AGTACTCATG TGCCTGTAGA AGAAAGGGGC CATTGCTGCT 900
GATGATAACA ATGATAGCAT CTAAGGTTTT ATAGTTCCCC AAATAATTTC ACATACACTG 960
TGATTTGATG CTTATAACAA CCGTGTGAAC TATGCAAAGT AGGTATTATT TCCCCATTTT 1020
AAGAGATGGG AGAATGGATA GTTAGTATTT TGAAAATTGC CAGACCCCAC ACTTATAAGA 1080
CTACATGTAT TATTAGTAAA ATTACTACTA GGGGACCCCA GCTATGAAAA CCTCTCTGGG 1140
AGATAGCACT GGTGGGTGAG GGGCAGCAGC TTCGGCTCTT GCCTCCTGGC AAGGGTGGGA 1200
TGTAATACCC TAAGCTCCAA CAGACTGGGG AAAGAGAAGG GGCTTAGAAA ACTGTCTGGG 1260
CTGCTGGATT TCTTTCCGGA GTTTCCCTCT CTCCTTCTAC TGTCAGCACG TCCCATCTTT 1320
TGCAACACCA GGGAGAAGCC TTTCCATGCC TCTTCAGCTC TTGGAATCCC TCCAGAAGCC 1380
CCCTCCCTCC TGAGTGGCAT CTAACAGGCC TGTCCAATAC TCATGCTACA GCTATGAGGA 1440
AAGAATAAAC CCTGCAGCTG CTTCAGAAGA GAAAGAAATC TCTTTTCAAA TGAAACCGTT 1500
TTTTGCAGCC CTGTGGAATT CATATTCTCT GTGATCTCCT TTGGATTCAA ATCACGGACC 1560
TGAAAGAGGG AGGGGAAGAA AACAGGTTCT TTTCCTCTGC CTGGGCCTGC CGTTCCCTCT 1620
GCCCTCCTAC ACTGGGTATG GACAGACCCC AAGGGACCAT GGTCTAGGTG TTGGCAGCCA 1680
GGCTGGCTCT ACAACACAAC ATGTCAGCTG CTCTGCTGGG CCTCTGTTTA CTCATCCATT 1740
AAATGAGGAG ATAAGATCTC CCTTGACTGG CTGTGAAGAT TAAGTGCACA AATATGTGTA 1800
AAGTGCACAA ATATGTCAAA TAAAAACTGA GACTGACACG TGGAGGTGCA AAATTAAAAA 1860
GGAAGCTTTG GTTAGTATCT CCAGAACCTG GCTAGGCACG GTGGCTCACA TCTGTAATCT 1920
CAGCGCTTTG GGAGGCCGAG ATGGGTGGAT CACCTGAGGT CAGGAGTTCA AGACCAGCCT 1980
GGACAACATG GCGAAACCCC GTCTCTATTA AAAATACAAA AATTAGCTGG GCATGGCAGT 2040
GAGCCCCTGT AATCCCAGCT ACTCAAGAGG CTGAGGCAGG AGAATTGCTT GAACCCGGGA 2100
GGCGGAGGTT GCAGTGAGCC GAGATCACGC CACTGCACTC CAGCCTGGGT GACAGAGTGA 2160
GACTCCACCT CAAAAAAAAA AAAAAAAAAA TCCAGAACCT GCAGATTGTG CCTCTGATGC 2220
ATCTCAAACA TCCAGGGCCA GGGAGAAAAT AATCTAAAGA AAAATACTAC TGAAAAAGAT 2280
TCCATTGCCA TGGCCCTCTG AGACACACAC ATTCTTATTC TCTTATTTTC TCTCTCTCTC 2340
TCTCTTCTTC TCTCTCTCTC TCTTTCTATC TCTCTCTCTC ACTCCCTCTC TCATTTACTC 2400
ACAAGGTCAG TGGCCCAGAC CCAGGCAGTT CTGGATAATC CCAGCTGTTT CTGACTCACC 2460
ACCATCCTCA GGGCTGGCTG ACTCACTCCA GGAAGGTTTT CCACCATGAA 2510