EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS118-15339 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr5:131769760-131772090 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2188962chr5131770805hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr5:131771883-131771894CCACACCCTCC+6.32
Klf1MA0493.1chr5:131771881-131771892GGCCACACCCT+6.32
RREB1MA0073.1chr5:131770856-131770876GCCCATACCAACCCCAACCC+6.1
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00037chr5:131769476-131776420Adipose_Nuclei
SE_09163chr5:131769539-131776436CD14
SE_11905chr5:131771443-131772099CD3
SE_18258chr5:131771017-131776294CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131771175-131772281CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131769618-131776268CD56
SE_22284chr5:131754357-131780344CD8_primiary
SE_23079chr5:131769694-131771398Colon_Crypt_1
SE_23079chr5:131771568-131772123Colon_Crypt_1
SE_23750chr5:131770391-131770966Colon_Crypt_2
SE_23750chr5:131771062-131771423Colon_Crypt_2
SE_23750chr5:131771671-131772131Colon_Crypt_2
SE_25340chr5:131769678-131772094DND41
SE_25784chr5:131769540-131776186Duodenum_Smooth_Muscle
SE_26597chr5:131769999-131771102Esophagus
SE_27859chr5:131769639-131772128Fetal_Intestine
SE_28909chr5:131768454-131771973Fetal_Intestine_Large
SE_30917chr5:131769816-131771306Fetal_Thymus
SE_31393chr5:131770034-131771484Gastric
SE_39368chr5:131770545-131771502Jurkat
SE_39368chr5:131771530-131772102Jurkat
SE_40726chr5:131769888-131771252Left_Ventricle
SE_40726chr5:131771413-131772138Left_Ventricle
SE_42103chr5:131769872-131772151Lung
SE_48659chr5:131770097-131771409Right_Atrium
SE_50034chr5:131769767-131771423RPMI-8402
SE_50051chr5:131769920-131772121Sigmoid_Colon
SE_52336chr5:131769663-131772128Small_Intestine
SE_53285chr5:131769955-131770781Spleen
SE_53285chr5:131771498-131772157Spleen
SE_54554chr5:131769980-131771486Stomach_Smooth_Muscle
SE_56265chr5:131771323-131776703u87
SE_59850chr5:131745223-131774088Ly4
SE_61542chr5:131744876-131774119Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_66244chr5:131770545-131771502Jurkat
SE_66244chr5:131771530-131772102Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr5131770427131770908
chr5131771667131772000
Number: 1             
IDChromosomeStartEnd
GH05I132433chr5131769658131776999
Enhancer Sequence
ACCACTCCCG GCTAGCAACC GGCTTTTTAC AAATAGCAGT CTATTGTGTA TATTTCTCTA 60
TGACAGTACA TAGAGACCTG CTGTCTTCTT TTTAAAGGCT GCTTGGTATG TATTCCACCA 120
CGTAGATGTA CTGCTAGTTC ATCTCCTCCC CTACAGATGA CCACAAAGTT TTTCAATGTC 180
CTGATAATAT TTATAGGCCA CTACATCCTC ATTTTTATAC TTTTATGCAT TTGTGCTAGT 240
GTTTCTATAA AATAGATTTC TACAATTGAG ACTGTTGAGT TAAAGGGTAT ATACATAGTA 300
AGTTGTATAT ACTTCCAGTT GCCCCTTGTT GAAACCTTGT ACCAATCAGT GCAGTGTCCT 360
TTTAAATGGT CTTTTCATTG CCTGTTGCTT CCCTGTCTCC CCACCCCCCG GCTCTTCACC 420
CTAGTGCTAG AATTGCTTTT ATGAAACTCA GATCTGACCA TGGCTTGCCC TGTTTAAAAT 480
ACCTCAGTGG CTCCTCACTG TCAGCAAAAC CCAAACATTC ATCTAAGCTC CTTCTCAGTT 540
GGAGTCCTCT GGGAAGCAGA CACCAAAACA GAATGAAAAG TGCAGAAGAT TTATTGGGGG 600
TAAGAAGAGC TAATGCCTAT GAAAGATAAA GGAGAAAGGA GCAGAAGTAC GGAGAGAAAA 660
GACAGCTTTC AGACTGCAGT CCAGATCTAA CTCTGGGACG CAAGAGAGGG AAGGATAATT 720
CTGTTGAAAG AGCATCAGAC TGTGATGCGG CTGTAAGAGT GTCTCAACGA GCCCAGTGGG 780
GAGTTCCAGC CAAAGATTGC CCAGGAGAAG AGTCGCACTT TGGGCAGAAA TGGACAGGCC 840
CGAGCAACCC TGCCATGTTC TGTCATTGGC TGGGGGCCAC CCAGGAGGCA ACATGGTCTG 900
ACTTGAATGG TGTGGATCCG AGGCTGCAGC CTGTCAGCTG TCTGCACTCC ATGCAACAGG 960
TCCTTTGAAT GGCATGTGTT CGTGGCTGCC ATAAACTGCA GCCTGCCTTT TAGCCTTACC 1020
TCCTTTGCTC TTGCTCTCTG ACCCCGTGTT CTGGCAACAC TGGCCTGACT ACACGCCGTA 1080
TCACATACAA CCAACTGCCC ATACCAACCC CAACCCTGAC CTTTGCTCAC TCAGTTCTTT 1140
CTGCCTGGAA TGCCACTCCT TCCCAGTTAT ACCCAGCAAA ATCCTAATGT GCTTTCAAGG 1200
CCCAACTTAA AAATCATCTT CTCTGGTTGA CCTCACCATG TAGAATTAAT TGTTCCTTGC 1260
TCCTATGGTG CTATGTGTAT ATTAGTACTT CCCAGATTGG AGTATTCTTA GCTGTTTTTT 1320
TCTCAGATTT TTGCCTCCTC TAAACCTAGC AAAACGTCAG CACACAGTAA ATGTTGACTG 1380
AGCTGTTTCC CTGCTCCTCG CAAAGCACCT TGAGGTTGCA GAATTCCAAC TCCCGGAATG 1440
GTTGGAAGCA CACAGTACAT GGTCAATAAG TGTTTGTTGA CTTGTCTGGG ACCTAGTATT 1500
GGTGGGGTGA GGTGGGCAGA AGGCTGCTGA GGGTGGGTAT TTACTGTTGT TGGGGCTCAC 1560
CAGTCTGGGG CCACATTGGA GTTTTAAGAC TAGAGCATGT CTTCCCCTGT TTTTATTTTT 1620
CTCCATGATT TGGAAAGACC CCAGAGGTGG GTTTTTTTTT TTTTAAGTAA TCACTTTATT 1680
GTCTCTGGTC AACAAATGAG AACTTTTATG GGTCTTCCCT TTTTCAACCA CATTTTCATG 1740
AGTTGGGATT TTGCATTTCT TCATTACCCA TTCTCCTTAT GGGTAAAAGA AGAGCCATTA 1800
TGATACCTAG GATGAGAGCT CCAGGTCAGA TGGGTAATCA TTTTCAGACT GGAGGCTCAT 1860
GGGATACAGG GAATTGGGAA GGTAGAAATG ATATTTTTCC TCTTCCTCTT TCCCACATCC 1920
ACCAATTAAA GAACTTCCCT GGGAGTGGAC CTGTGGGAAG TGGCTAAGGG TTTCCGGGGT 1980
GGGTACAGCA GGGAGTGACA TCAGGGCGTG GTGGGGATGA GGTGGGTGGA GAGGACAAAG 2040
AGGGACTCTC CACCTTCCTT TGGATCTATG AGGATGTTCC TTGGCCACTG TCCCTCAGCA 2100
GAAGGAGGCT AGAGCTGAGG TGGCCACACC CTCCACTCAT TTTCAATCCC TTCAAACTGT 2160
CAGGCCCTCA GAGGAAACCC TAGGGTTTCC CCACCAAGAT GTAAGGGCTG TGTGCCTCTG 2220
CCTTCTCTCT TAGGGTGGTC AGCACAGGTG GAAGCAGGGA GGTACTGGGC TGAGGCTTCG 2280
GTTGTCAGTG CTAGCTTGAC AGCAGTTAAG AATTTTTTTT GTTTTGTTTT 2330