EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS190-01243 
Organism
Homo sapiens 
Tissue/cell
Treg_cell 
Coordinate
chr1:223913280-223916110 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr1:223914582-223914593GGTGACTCATC+6.32
FOSL2MA0478.1chr1:223914581-223914592GGGTGACTCAT+6.14
JUNBMA0490.1chr1:223914581-223914592GGGTGACTCAT+6.32
JUNDMA0491.1chr1:223914582-223914593GGTGACTCATC+6.62
NKX2-5MA0063.2chr1:223915940-223915950CTCAAGTGGT-6.02
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00224chr1:223912311-223916909Adipose_Nuclei
SE_01908chr1:223913738-223914955Aorta
SE_02306chr1:223913344-223915961Astrocytes
SE_04026chr1:223913451-223915326Brain_Anterior_Caudate
SE_05036chr1:223913560-223915403Brain_Cingulate_Gyrus
SE_05972chr1:223913207-223916372Brain_Hippocampus_Middle
SE_07996chr1:223913125-223915466Brain_Inferior_Temporal_Lobe
SE_09681chr1:223912826-223918041CD14
SE_19702chr1:223913106-223916325CD4p_CD25-_Il17p_PMAstim_Th17
SE_24051chr1:223913880-223914466Colon_Crypt_2
SE_26209chr1:223912988-223915695Duodenum_Smooth_Muscle
SE_26925chr1:223913192-223915372Esophagus
SE_31491chr1:223913141-223916265Gastric
SE_34545chr1:223913070-223916058HCT-116
SE_34979chr1:223912930-223916086HeLa
SE_36294chr1:223913510-223915892HMEC
SE_37129chr1:223913319-223916436HSMMtube
SE_38254chr1:223913007-223915923HUVEC
SE_38957chr1:223913198-223916265IMR90
SE_41495chr1:223912854-223916323Left_Ventricle
SE_42269chr1:223912507-223916406Lung
SE_44530chr1:223913197-223916987NHDF-Ad
SE_44904chr1:223913680-223916262NHLF
SE_45872chr1:223913083-223917105Osteoblasts
SE_49408chr1:223912976-223915760Right_Atrium
SE_50365chr1:223913039-223916033Sigmoid_Colon
SE_51879chr1:223913896-223915223Skeletal_Muscle_Myoblast
SE_53249chr1:223913106-223915207Small_Intestine
SE_55958chr1:223913015-223914574u87
SE_55958chr1:223914578-223916004u87
SE_63671chr1:223913673-223915261HSMM
SE_64794chr1:223913313-223915321NHEK
SE_65644chr1:223913370-223915937Pancreatic_islets
SE_67677chr1:223913015-223914574u87
SE_67677chr1:223914578-223916004u87
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1223914239223914747
chr1223913851223914937
Number: 1             
IDChromosomeStartEnd
GH01I223722chr1223910120223916233
Enhancer Sequence
TGGCACATCT TGAATACCCG ACTGGGTCCC AGCTTTAGCA CTTGACATTG GCGGCCACCT 60
AAGTTTTGGA GAGGGGTATG ACAGAGGAGG TGGTGTCCCA GGGGGAAGGT CCGGAAACTC 120
AGAGGAGTTT CCTGCTGTAA TTTTCTTTGG TCACACAATG GTCATGGCCT CCTGATGTTT 180
CCCACAAAGG GCCAGAGGCC CTTCAGTGCC AAGGAACGTG GACTCTCTCC TATCCCAGCA 240
CATACACGTG CTTCCAGTAC CTTGTGATCT CTAGCCATAA GTTTCCACTC ACCCATCTGC 300
GAAATGGGAA CAATGACGAT GTTTGCGTCC TTTCTTTTTC TTTTCCTACA ATGCAGGGAA 360
CTTTAAGACT ATGTGACAGA AAGGTGCCAC TGGAACCCAG GGCCTCGTGG GTTTCCTCCG 420
TCTCTCGGGA GACCAGGATC CGAGTGAGAA AGTTTCCCAC GTTCATTCTT GTTGGGCCCA 480
TTCTCAGGAT GATGTTTCTC CTGTATTTTG CTACCCCAGC CCAAGCAAGA CTAGTAGTTC 540
AGCTTTGTGA ATCCCCTCAG GAAGTCAGGA AAATAGATAC TGTCTTTGGG CTTCCTCCAG 600
GAGCTAAGAA AGGAGAGTTC CTGAAGAGCA GGAATTTAAG ACAGGAATTG GCAGCCGAGG 660
GCAAGGTTCC ACCTCCTCCT CCCTTCTTCT GTGGGGTCTG TGATGAGAGC AGGGATGGGG 720
AGGAAGAGGG TGGGTTTGCC TGCGCCTGGG GGGAGGGCAG CCATCAGGAA GGAGCAGCCA 780
CCTCTGCTGG GGTACTGGAG ATAAAAACTC TGATATTGAC TAGTGACCGT GGGGGCGATG 840
GCCCAGGAGG GTCAGGGCTG CAGGGAACAG GGACACAAAA ACGACAAAAC ATGCAACAGG 900
TTATGTCCTT CTGGTCCAGG GCACGGCTGA GACAGGCAAG GGACTAGAGA GAGGAAGAGT 960
GAATGTCAAG CCCCAGCACC CTCGCCTCCC TCCCATCCTC CCTTTTAGGG CCTCCCTTCT 1020
GGCAGATAGG GCAGGGAGAA GGGAAAGGAA AGGCCTGGGA CACGTGGTTT GGATCACTGG 1080
CTGTGGCTCA CAGTTCTGAT GTGTGTGCAG TTTAGGGAAG GAGGCTGAAG ACTTCTTGTT 1140
AATAAGGGTG GGGCATGAGT AAAATGGAGG ATCTGCCCCC TCCCCTCCCA GCCCCTGATA 1200
CAAATGAAGG ATGATTGTAC ATGCATGGGG AATTCCACTT TGGGGGTATC CTTTTCTGGG 1260
CTGCTGCCAG ACTCTGAAAT GAGTAACAAA GGGATGGCCC AGGGTGACTC ATCAGCTACC 1320
CTCTCGCAGG CCTAGCACGC TGGCGGGGTG TGCATTTCCT CTAGAGAAGC CCCTCCCTGC 1380
CAGTTTCAGA GGGATGGCCC TGAATTGGCT TTTCAGAGGT TCCTTCTCCT CCCTTCCAAA 1440
GCGAAGACCC ACAGCTGCCT GAAAATGTGG CTCTCCGCCT TCTTGGGCTG CCTAGGACCT 1500
TGAGAGATGT GTCTCTCTGG GACAGGGTGT CAGGTCTGCT GGAGATTGTT AAAATGCTGT 1560
TGTCTCAGGA AGGGTGAAAT TTAGCCAGGA GCAGTCTTCA GTAGCTTGGT CTGTTTATCG 1620
TGTATCTAGC TGTCAGCATG CAAAACAAAA GAACAAAAGG TCTAAAGAAA TATAACGCAA 1680
AACAGGTACG ATTTGAGATC CATCAGGGTT TCTCAACCTT GGCACAACTG ACTGGATAAT 1740
TGTTCATTGT AGGGGGCTGT CCTGTGAATT ATAGGATGTT TAGCTGCATC CTTGGCCTCT 1800
ACCCACACAC CCCCGTGTGC CACTCAAAAA TGTCTGCAGA CCTTGCCAAA TGTCCCCTGG 1860
GGGCTTGGCG GAGTTGGGGG GTGCATGGAA TGCCCCCAGT TGAGAACCAC TGGCAGAGCA 1920
GGAGTGAAGG GGGAGGTACT GTGGGGGTCA CTGGGCACAC AGAATGCCAT TTGGGGAGCC 1980
TGGTGCAAGG GAGTGGCCGG ATGGGAGGTA GGAATAGCAG TGGTAATCAG TAGGTGAGTT 2040
GCTGAAGACA AACTAAATAT TCTTTCCAGC ATTGCTTCAA TCTAATCCAG CCGCAAGTAT 2100
GAGTAAATAC TGTAGGAAAG GAGAAAACAT TGCATGTACG GGGTCAGGGC AGCATTGCTG 2160
GGATATTTGA GCCTGTGGGA GGGGAGCTTC AAGCTTCCCA CTAGCATTGG GAGGAACACA 2220
GCAAAGGAGG AGAAGGGCCC TCCCTGCTTC TTGGAGAATG GTTCCACTGG CAGGCCATTC 2280
CGTCTGCTCA GCTTCCTAGC TCAGGTGCCT TTCCAAACCA CACATCAGCA GGGAGACAGT 2340
GGGAACATCT CAGGTCCAGG GTACCTTGGG AACTGCAGAG CAGCTGGGTG GCCTGACACT 2400
GGCATTTCTC AGTGTTGGCT CCATTCTCTT GCTGGCACCC CCAGGTGGGA GACTCTGTTA 2460
GCAGGTGTAT CTTACTATCC CTGGCTCCCT GGTATGCGTT ACAGTTCAGA CTCCCAAGCA 2520
CAAGCTCCCT GTTTTGTCAC ACCTGTATCT AGTGTGTAAC AATCCACCCC AAAACAAATG 2580
GCTTGAAACA CAAGGCATTT TGTTCTCTCT CATGGTTCTG AAGGATGACG GGGCTGAGCT 2640
GGGCAACTCT CTCCCGCTCT CTCAAGTGGT TGCAATCAGA TGGGGATGGG GACAGAGTCA 2700
TCTGTAGGCC CCCTCAACCA CATGTCTGGT GCCCGGGCTG AAGGGTGGAT CAGCAGGGGT 2760
CCAGGGATCT CTGTCTCTTT TGTGGTCTCC CCATCACAGG GACTTGAAGG TAGCTGAACA 2820
TCTTACAGCA 2830