EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS044-08665 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr22:47130040-47131640 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXC1MA0032.2chr22:47130644-47130655ATATTTACATA-6.62
Foxa2MA0047.2chr22:47130464-47130476TGTTTACACAGG+6.14
RREB1MA0073.1chr22:47130966-47130986CCCCCCAACACACACACACA+6.69
RREB1MA0073.1chr22:47130968-47130988CCCCAACACACACACACACA+7.29
SOX10MA0442.2chr22:47131413-47131424AAAACAAAGGA+6.32
Sox3MA0514.1chr22:47131413-47131423AAAACAAAGG-6.02
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_09349chr22:47130192-47135971CD14
SE_14697chr22:47130289-47135628CD4_Memory_Primary_7pool
SE_17674chr22:47129977-47136955CD4p_CD25-_CD45RAp_Naive
SE_17901chr22:47129479-47137350CD4p_CD25-_CD45ROp_Memory
SE_18695chr22:47129530-47134167CD4p_CD25-_Il17-_PMAstim_Th
SE_19505chr22:47129264-47136199CD4p_CD25-_Il17p_PMAstim_Th17
SE_20325chr22:47129975-47135578CD56
SE_23520chr22:47130719-47132305Colon_Crypt_1
SE_24287chr22:47130679-47131949Colon_Crypt_2
SE_27442chr22:47130654-47136087Esophagus
SE_28432chr22:47129751-47141198Fetal_Intestine
SE_29215chr22:47129758-47141281Fetal_Intestine_Large
SE_31641chr22:47129922-47130667Gastric
SE_31641chr22:47130718-47135958Gastric
SE_38281chr22:47129860-47135670HUVEC
SE_40789chr22:47129770-47139213Left_Ventricle
SE_42260chr22:47130597-47139109Lung
SE_48916chr22:47130614-47133016Right_Atrium
SE_49561chr22:47130813-47132963Right_Ventricle
SE_50233chr22:47130014-47135867Sigmoid_Colon
SE_51682chr22:47130699-47137805Skeletal_Muscle
SE_52427chr22:47129806-47136051Small_Intestine
SE_53517chr22:47130708-47132392Spleen
SE_58383chr22:47122081-47199614Ly1
SE_62483chr22:47129710-47188820Tonsil
SE_65427chr22:47130748-47133722Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr224713033347131449
chr224713006347131516
Enhancer Sequence
GCATAGCCCC TAAAGGGTCA GGGTGTCTTT ATCCACATAG TCAAGGTGAA TGGACTGCAA 60
ACTGTCCAGA AGCCCATCAG CAGGTGAACG GATACACTAG TGCACCCACA CAATGCAATA 120
TGACTTAGTA ACCAGAAAGA AGGAACTGCT GACATGATGA ATCTTAAAAA AAACAAAATG 180
AGATAAAGCA GCCGGGCACA AAGACGTGCA CATGGCATGA TTCCATTTAC ATGAGATAAA 240
GCAGCCGGGC ACAAAGACGT GCACATGGCA TGATTCCATT TACATGAGAT AAAGCAGCCG 300
GGCACAAAGA CGTGCACATG GCATGATTCC ATTTACATGA AACTCTATTA GCATCGTGCC 360
TGTCCCTGGT GAGAAAACAG CCCAGGGCCC AGGAGAAGGT GCTGGGCTGC TGCGATCCGG 420
GTGATGTTTA CACAGGTGCA CACAATTATC AAAATTTAAC CAACTATGTG CCTTAAAATG 480
TCTGAGTTTT ATTGCATGCA ATTTAGACCT TGATAAAATC GATTTTTAAA AATCATGTCT 540
TAGGAGAGGA ATTAGTAGCG TGGAAAACAC TCTGCAGTAT GTTTTCTCAG CTTTTCTTTC 600
ATGCATATTT ACATATACAC AAATACCAAA TATTAATCAC GTCTAAGTCG AAGAGTGACT 660
TTTTGTGTAT GCTTTTCTGT GTTTTCTCGA TATTATTAAA TCAACATGAC TTACTTTTGT 720
AAGCAGGAAA AACATTTTTT TAAAGTATCT GTGGCATGCC TATGTTTTGC CAGGCACTTT 780
GCAGGGTGTG CTGAGGACAC GCTTTATAAA CACAGTACTG ACCTGCCCAA CGAGTTCACC 840
ACCAGCCTGG GACATCCCAA GTGGGGTTGG TGGAAGGAAG GGGAGGATCC TCCCACAAAG 900
GTAGAGCCTG GGCAGTAGTC CCCTCACCCC CCAACACACA CACACACACA CACACACTCT 960
TCCCATTCCC AACTCTAAAG GAATAAATGC AGGGTTTGTC TAAGTGTGTT TTGCGACAGT 1020
CAGGGGAAAT AACCCAGATA TCAACTCAGT GTTTCCAGTT CAACGAGCAT GACCCACTTC 1080
AAGTTCCTGT TTTCGTCCTG CCCTACTTCC CACCAGGCTG GCGGCCCAGG GCACTTGCTG 1140
TCGCGGCTTC CTCAGGTGCA GACCTCACCC AGGCCCAGGA AGCTGCAGCG ATCCAAATTG 1200
CTAGTCCTTG TCTGTGCTCT TGTACAGTCA GTCACTGTCC CAGCATGATG ACCCACTGAC 1260
GAAAGTGCAC GTGCCTGGGT TCAAAGCCAG CTCCCTCTGT ACATCACTGC CTCTGGGCCC 1320
AGTCAATTCC CACTCCTACT GTCCACATCT GAAATAGGGG TGATGCTACG GAGAAAACAA 1380
AGGAGTCGGA ATAACTAAGC GGCCACCCCA GCAGGGCACA CACAGTGGCC TTGGCTTTGT 1440
CTTTAGCCCA TTGGTCACCT GGAGCTCCAG GGCTGCTCCT GCCTCATCTC ACAGGTCCTC 1500
CTAGGGCCAG TTTTTGCACA ATTCTCCACC TCTCATCATT CCTCAACCTA ATCAATCCCA 1560
GTGTGCCCAG ATACACCTGG GGGAATGGGG AGGGCTGGGC 1600