EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-03131 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:153916910-153918770 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUNMA0488.1chr1:153917218-153917231ATGACATCATTCA-6.41
JUND(var.2)MA0492.1chr1:153917217-153917232CATGACATCATTCAT-6.33
KLF4MA0039.3chr1:153917550-153917561CCACACCCTCC+6.32
RFX2MA0600.2chr1:153916916-153916932GGATGCCATGGCAACC+6.08
RFX2MA0600.2chr1:153916916-153916932GGATGCCATGGCAACC-6.12
RFX5MA0510.2chr1:153916916-153916932GGATGCCATGGCAACC+6.33
RFX5MA0510.2chr1:153916916-153916932GGATGCCATGGCAACC-6.55
ZNF263MA0528.1chr1:153918437-153918458GGAGGAGGCTGAGGAAGGAGC+6.23
ZNF263MA0528.1chr1:153916949-153916970CCCTCCTCTTCCTAGTCCTTC-6.49
ZNF263MA0528.1chr1:153918434-153918455GGGGGAGGAGGCTGAGGAAGG+6.89
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_07112chr1:153916510-153920184Brain_Hippocampus_Middle_150
SE_13301chr1:153916379-153919168CD34_Primary_RO01480
SE_13979chr1:153916328-153920017CD34_Primary_RO01536
SE_17279chr1:153916800-153919789CD4p_CD225int_CD127p_Tmem
SE_19751chr1:153916106-153919855CD4p_CD25-_Il17p_PMAstim_Th17
SE_20550chr1:153916049-153920190CD56
SE_22844chr1:153916133-153920212CD8_primiary
SE_27263chr1:153916630-153920158Esophagus
SE_41224chr1:153916145-153919925Left_Ventricle
SE_42677chr1:153916172-153920139Lung
SE_49113chr1:153916189-153919933Right_Atrium
SE_50562chr1:153916550-153920149Sigmoid_Colon
SE_53266chr1:153916690-153920078Small_Intestine
SE_53527chr1:153916236-153920284Spleen
SE_59593chr1:153916527-153921857Ly3
SE_60702chr1:153916094-153937455DHL6
SE_62719chr1:153916077-153937522Tonsil
SE_65739chr1:153916330-153917168Pancreatic_islets
SE_65739chr1:153917349-153918800Pancreatic_islets
SE_68155chr1:153917025-153964411TC32
SE_68156chr1:153917025-153964411TC32
SE_68157chr1:153917025-153964411TC32
SE_68158chr1:153917025-153964411TC32
SE_68159chr1:153917025-153964411TC32
SE_68160chr1:153917025-153964411TC32
SE_68161chr1:153917025-153964411TC32
SE_68162chr1:153917025-153964411TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1153917018153917841
Enhancer Sequence
GGCTGGGGAT GCCATGGCAA CCAGGGTACC CTCTTGCTCC CCTCCTCTTC CTAGTCCTTC 60
CAAAGAAAGG CAGGATAAGG GGTCGGCCAA TCCTGAACTC TTCCCCCTGT GACATCACTG 120
CCCACCACAG CTTCTTAAAG AGACCAGATC CCTCCCACTT AATGGTCCTG GCACTCCCCT 180
CAAAGAACCT AAACTCCACC ACACACAGCT AACCTGAGCT ATGACATTCA CATTGTCCAT 240
GTGTCCCTTT TAAAGGCTCA CCAGTTATAA CATCACAGAG ATCACAATCT TTTTTGTAAT 300
AGCCTTCCAT GACATCATTC ATGCTGGCCA TGACATCATA CCAACCTTAC AGTCTTTTCA 360
AGGGTTTCTG ACCTTCCTAC TCTAGTTATG ACACCATAAG AACCTTGTGA TCCTGCCAAT 420
GTTCTTAAAG AGCCCACTCC TAGGTTTTTA AGAGGACCCC ATGGGTTTCT GAGAAAGCCC 480
ACAAAACCCA AGCTTTAAGA GTCTTTTCAA CGAACCCAAG TGTCCTTTCT CCTAGCTTAA 540
CTCCACCAAT CTGGCCCAAA ATCCAGTGTT CTCACACCTC CAGGATCCTT AGGTAGCTCG 600
TTAGATCCAA AGCAGTTGTG AGAGACAAGT CCCGGCCATC CCACACCCTC CACCATGGAG 660
CCCAGAGACA GAAACAGGCC CACAACAGCC TAGTTCTCAC CTGCCTCCAT GGCCCAACCC 720
CGGGGAGTAG GAGCCCCAAG GGTCCTGAGG CGCCCCAGGG TGCAGAAGCT GGGAAAAAGC 780
CTGGTGGGTA GCTCGCAGCA GGGGCCCAGA AGCGTGGGGG GTGCTTCAGA GGGGAAGGGA 840
GGTTACTTCC TGAAACAGTG GAGGGGAAGC TGCAACTCAG AGGAAGTCAG CCTATGGGTG 900
TGTGTGGTGG CGGTGGCGGT GGTGGGGTTA CCATTGAAGG TGCCAGCACA GCATTACGCC 960
AAGTTGGAAT CTCAGACTAT AGGATCCTGA GCAAGGCAGA GGAGGCTCAG AATGGTTCCA 1020
GGATGTGCAG TCCTGCTAAC CTCCTGCTGT TCCCCCAGAG AACAGGGAAT AAGGAATCTC 1080
ATAGAGCCAG GCTGGCTTTC TTCATCACCT GGCCTCTGGA CACACACACA CACACACACA 1140
CGCACACACA CACGCACACA CGTACACACA CCAACCCCAG CTAAATTTAG ACTCCACTTC 1200
TGGGAGGTAA AGCCAGGAGT CAGCGTCAGC CTCTTGATTT AATTCTGGGG CACAGACCTG 1260
TCCCTCATCC ACTGAGGGCG AATGGGAGCC CTATGCCCAA GGCAGCAGGC AGAGGCCATT 1320
AGGTGGGACC TTCTGAGGGG CAAGTGGGTG GCACCCATCC GCAGGACCTG CGCACCGGGG 1380
CCTCCCCTCA CCAAGCCAGG GAAGAGTCCT GCAGAAAGCA GCCCTTTCTC CCTAGGGAAG 1440
ACAACGGGCA CAGGGCCCAC TCCGGGTCCC CACGCCCGCG TGCCGGGTGA CGGGAAGTTC 1500
GGGTTGGGGC AGAGGGCGCG CCGAGGGGGA GGAGGCTGAG GAAGGAGCAG GAGGGCAGAG 1560
AAGCAGGCGC GCCGGCGGCC GAGGACGTGA CGGCAGCAGC GCCGGCCGCC GCGTGACCCA 1620
AGCGGGAGGG AGGGCGGCTC CGACTCCGGC ACCCACGGGA GCAGAAGGGG GTGCAGGAGG 1680
CCGGGCACGG CGAGCTAATT GCGGGAGGTG CCCTCCCCTC CACTTTCACT TCCCCAGGAG 1740
AGAGGAACCG GAACCAGATG TGCAGTGAGG GACAGCAGCT GGGGGCCATC CCCCACCCCG 1800
CCTGCCGCCC GCGCTCCCTC CTGCCCGTCC CCGCCTGCCG CCCAGCCCGG TCCAGCCCCT 1860