EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS087-06387 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr14:65186380-65189290 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxq1MA0040.1chr14:65186790-65186801AATAAACAATA-6.62
RREB1MA0073.1chr14:65188779-65188799TCTTGGGGATTGTTTGGGGG-6.44
SRFMA0083.3chr14:65187797-65187813TTGCCATATAAGGTGA+6.43
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_01667chr14:65180847-65190201Aorta
SE_03251chr14:65186793-65188858Brain_Angular_Gyrus
SE_03953chr14:65180662-65189028Brain_Anterior_Caudate
SE_04856chr14:65180505-65197762Brain_Cingulate_Gyrus
SE_05821chr14:65180438-65199821Brain_Hippocampus_Middle
SE_06781chr14:65180403-65192060Brain_Hippocampus_Middle_150
SE_07938chr14:65180667-65190097Brain_Inferior_Temporal_Lobe
SE_08852chr14:65187988-65188330Brain_Mid_Frontal_Lobe
SE_19856chr14:65187027-65188984CD4p_CD25-_Il17p_PMAstim_Th17
SE_19856chr14:65188989-65195748CD4p_CD25-_Il17p_PMAstim_Th17
SE_20478chr14:65185982-65194236CD56
SE_22874chr14:65186008-65194196CD8_primiary
SE_23289chr14:65182158-65189042Colon_Crypt_1
SE_24426chr14:65186024-65188737Colon_Crypt_2
SE_26750chr14:65181719-65194103Esophagus
SE_27717chr14:65181723-65189060Fetal_Intestine
SE_28783chr14:65185739-65188904Fetal_Intestine_Large
SE_32308chr14:65185993-65188715Gastric
SE_36148chr14:65181584-65194566HMEC
SE_47632chr14:65186035-65189003Pancreas
SE_49272chr14:65187548-65189045Right_Atrium
SE_50477chr14:65180818-65190196Sigmoid_Colon
SE_54434chr14:65186992-65191038Spleen
SE_57093chr14:65186048-65187048VACO_400
SE_57093chr14:65187178-65188964VACO_400
SE_57603chr14:65186014-65188960VACO_503
SE_64475chr14:65185799-65194369NHEK
SE_65298chr14:65181865-65199543Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr146518777165188902
Number: 1             
IDChromosomeStartEnd
GH14I064714chr146518085865194899
Enhancer Sequence
GGGCCCCTCC ACACCCACTT GGTTCCCACC GAGATTCTCC AGTGCCTTTG AACCTGAGGC 60
AGTAGTAAAA TGCAGCTTCC TCCTACCCAC CCACCCCGCT CCAGCCTAGA GGCCTCAAAA 120
CAAGCAGCCC CTGAAATGGG GATGAGGCCG GAAAGATGGC GAATTTGCAG GGCTGGGTTC 180
TTGAACTTTG CTGGTAAGTA GCAGCGGTCC TGTGAACCTT TTTGACCTCA AGATGAGAGA 240
GGTGGGGCCT CTGGGAACTT TGGATCTGTC TGTGATTTCC AGGGGGTAAT TTCTAGTAAC 300
ACCTTTTAGG GCTTTCTTTG GCTCTTCCGG TTTTGGGGCA CATTGCATAG TGACAAGTTG 360
TGCTGGCAGC CAAGTTACCT CTACACTGGC TGTGAACAAG AGCAATTTAT AATAAACAAT 420
ACTTGCCCCC ATTTGGCTTT AGCATATGTT TACATGAAAC TTCCTGGCAG ATTGCTTTTC 480
CTGGGACATT TGCAGGGAGA CCAGATCATC ACAGCCCCTT TTCTAAACTT GGCTACTTTC 540
CCCTTCCTCC CAGTCTCTTG TGGCTGGTCA CCTAGTATGT AGCCCAGCGG GGCAGCTATG 600
CCGTGCTCTA GCTCCCTGTC TGGGGCCAAG TAGGATGGGA CTACCGGGGT GAATGAGCAG 660
TCATCAATCC TGGCGCTTCT TGGTTGATCG GAAACTTGCT GGCAGTGACT AATGTGGAGA 720
CTCATTAGGC TAGGAGGAAC TGGCTTTGGT CTTGACCTCA CCCACTGTTT ACCTTTCTCT 780
TGACTGTGTG AGTGGTGAGC TCATCCCGGC GCCATCTCAG AGTCCTTCCA GCAGGCATTT 840
ATTGAACACC TAATGTGCCT TGCTCTCTGG GGCTGAAGGG AAGGTATGGG AAAGAAGGCC 900
CAGCCCACTG GGTTTTACTG TATTGTCCAG AAGAGATGCA TGTACATATC AAGCCCCAAG 960
ACCAATGCTT TAAGTGATAG GGTGTTTCGA GTTCAGAGGA GTATATTACT TCCCTATTGC 1020
CACTGTAACA AATTCTGCAA TCTTAGTGGC TTAAATCAAC ACACATTTGT TGTCTTAAAG 1080
TTCTGGAGGT AAGAAGTCAG ACTGGGTTTG CATGGCTGGG TTCCTTCTGC AGGATCCAGG 1140
GCAGAATTTG TTTCCTTGCT CTTCCTAGCT TCCCAGGCTG CCTGTATCCT TGGCTTGTGG 1200
CCCCTTCCTC CATCTTCAAA GCCAGCAGTG TAGCATCTTC CAGTTCCCTT CTCTCTGTCC 1260
CTCTGCTTTT ATTGTCAAAC TTCTGTCTGA CTCTGACTCC TGCCGGATTC CTCTTACGAG 1320
GAGCCTTATG ATCACATCAG GCCCACCGGG CTAATCCAGG ATAATCTTCC ATCTTAAAAT 1380
CCTTGATTTG ATCACATCTG CCTTCTATGT GTCCCTTTTG CCATATAAGG TGACATTCAT 1440
AGGTTGAGGG TCAGGCTGTA GATATCCTTG GGTGGGGGCA TTATTCAGCT TACACTAGTG 1500
TGTATGTTGG GAAATGGTTG AGGAGGCCTT TCTCTGAAGG AGATGATTGC TAAATGTGTA 1560
TAGGCAGAGG GTCTGGGGAC ACATTCCAGG TTTGGGAGAC AACATGGGCA CATGTTGGGT 1620
AGGTGGGGAC AGGGGGGTGT AGATGAACAG CCCTCCCTCT GAGCTAGGTG CCTGGCTTTC 1680
CTTTCCTTCC AAGGTCAGGC CGAGGGAACT TTCTGGACTT CAGTTGCAGG CCCAGGCTTT 1740
CTCCTGGAGT CCATGTGGGA GGGCTCCCCT GGCAACACAA TCCTTTTCCT TCCTGGCAGC 1800
TGTGGTCCTG CTGCAAGGGA CCCAGCCAGA CTACATGGGC CCTGCTGCTC TTAGGTGGTG 1860
GGAAAATGCA TTCCTGAGGG AAAATGAATT TGAACCAGCT GGGCTGGGTT TGGGTGGCCC 1920
AGAAACCTTG GTCACACTGT TGGCACAGCC TCTGCAGGCA GTCACGTTGC TCACATGCAC 1980
ACAAAGTCAC TCCCCGGGGA GCCTTCTCTC GCGCTTTATT ACGGTGCTCA GGGCTGCTGA 2040
ATCTCCAGGA GGGATGGGAG GGGTCAGAGT GAGGAAACTG CTGGGAAAGG GGGCAAGGGT 2100
CCCCTAGGAG GGGGTCCTCC CCTCCCCCAG GAGAGCCCCT AGGGTGCAGG GAGCAGTGGG 2160
AACACACAGG CAAGAGCTGG GCCTCTGGGG ACAGTTTGGG AGCCGGGTGG CCCAGAGTGG 2220
TGCCGAGCTG TGGGTAAGAG CACAGCCGAG GGATTTCACC ATCTTAGTTG AGATCTTAGT 2280
TGAGAGAGAT CTCTCTCTGG AAGTTCACAT TGCTCCCACA CTGTTTTTTC TGGAAAAGTT 2340
ATAGCTTTTC TCTATTGCTT CCTTCTGGCA CCCTTTTTGA AGGGATTCCG AAAGTGCCGT 2400
CTTGGGGATT GTTTGGGGGA AGGACAAAAG CCGCTGGGCC ACCCTGGCTT TGAGAGCCCT 2460
TGGAATGTTT AGCAGATGAT GTAGTTGAGG GATGAAGGCC ACACAGGAGG GCTGCGCCAT 2520
CGCCGTTCCT GAGTGAGGAC TTTCTTTCTT CCTTTCTTTT TTTGTTTTTG AGATGGAGTT 2580
TCGCTCTCAT TGCCTAGGCT GGAGTGCAGT GGTGCGATCT CAGCTCACTG CAACCTCCTG 2640
GGTTCAAGCA ATTCTCCTGC CTCAGCCTCG CGAGTAGCTG GGATTACAGG TGCATGCCAC 2700
CACACCCGGC TAATTTTTGT ATTTTTAGTA GAGATGGGGT TTCCTCATAT TGGTCAGGCT 2760
GGTCTCAAAC TCCTCTCAAA CTCCTGACCA AAGGTGATCC GCCCACCTCG GCCTCCCAAA 2820
GTGCTGGGAT TACAGGCGTG AGCCACTGCG CCTGGCCACG AGGACTTTCC CTGTGTGCAG 2880
GTGCCGTGTG GATTCCTCCC CAGCTGGGGC 2910