EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS045-14206 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr12:6289400-6292040 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs4991925chr126290434hg19
rs4290286chr126290541hg19
rs7342306chr126291093hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RxraMA0512.2chr12:6289509-6289523TGACCCTTAACCCC-6.23
SP1MA0079.4chr12:6291837-6291852AGAGGGCGTGGCCTG-6.15
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00985chr12:6289433-6290385Adrenal_Gland
SE_00985chr12:6290507-6292062Adrenal_Gland
SE_01613chr12:6287777-6290458Aorta
SE_01613chr12:6290594-6292119Aorta
SE_03988chr12:6287691-6290093Brain_Anterior_Caudate
SE_03988chr12:6290792-6291792Brain_Anterior_Caudate
SE_04905chr12:6289324-6293306Brain_Cingulate_Gyrus
SE_05857chr12:6287388-6293430Brain_Hippocampus_Middle
SE_07876chr12:6289745-6293464Brain_Inferior_Temporal_Lobe
SE_23086chr12:6289496-6290357Colon_Crypt_1
SE_23086chr12:6290753-6292057Colon_Crypt_1
SE_23760chr12:6289538-6290171Colon_Crypt_2
SE_23760chr12:6290811-6292000Colon_Crypt_2
SE_24754chr12:6289387-6290267Colon_Crypt_3
SE_24754chr12:6291005-6292084Colon_Crypt_3
SE_25881chr12:6290586-6291938Duodenum_Smooth_Muscle
SE_26531chr12:6287925-6290403Esophagus
SE_26531chr12:6290619-6292172Esophagus
SE_27879chr12:6290695-6293924Fetal_Intestine
SE_28805chr12:6290511-6293953Fetal_Intestine_Large
SE_30052chr12:6288016-6290605Fetal_Muscle
SE_30052chr12:6290681-6292144Fetal_Muscle
SE_31631chr12:6289050-6290342Gastric
SE_31631chr12:6290651-6293026Gastric
SE_34881chr12:6288010-6291925HeLa
SE_37709chr12:6286475-6292578HSMMtube
SE_37940chr12:6286549-6293824HUVEC
SE_41013chr12:6288021-6292951Left_Ventricle
SE_42122chr12:6287877-6292200Lung
SE_48662chr12:6287969-6292096Right_Atrium
SE_50072chr12:6287999-6290419Sigmoid_Colon
SE_50072chr12:6290476-6292094Sigmoid_Colon
SE_52457chr12:6287948-6292107Small_Intestine
SE_53862chr12:6287321-6293849Spleen
SE_54512chr12:6288437-6293993Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1262913586291755
Number: 1             
IDChromosomeStartEnd
GH12I006177chr1262869856293820
Enhancer Sequence
GGGGACACAA CACAACAGGT GTGCCGTGAC CGAGACAGAG ATGGGAGGAA CAGAAAAAGC 60
CACCCTGACA GGCAGCATGG GAGGGGTGAT GAGCAAGTTC TTGTTTTGTT GACCCTTAAC 120
CCCTCTGTAC TCCCTACAGG AGCCACTTCC CTGGCGTGCT TCCCCAGCCC GGCTGACTCA 180
CTGGACAGGA AAAGGAAGGG CAGGAATTCA GGCCGATGAG CCAGGGACCC TCACCTCTGG 240
CCGGGCCTGG CACAGCCTCC TGGGGAGCCC CCGCACACCA GCCCTCCCGG CACCACTCGG 300
TGTGTCCTGC CTGGCTGATG GGCAGCCACG TATGCCCCAC CCTCCCCTGA CCGTGCCCAC 360
TTACCCAGGG GCCCAGCTGT CTTGGCTGGC AGGCTTCCAT TGCAAGTCAC TCCTCCATCC 420
ACACAGATCA CTCACGTCCC TCATTCCGTC CCTCGTTCCA CAGAGCGTGT TGACACCCAC 480
TGCGGGGCAG GCCTGGCTGC AGGCCTGGAG ATGCAACAGC AGCAAAAGGA GCAGCCCCTG 540
CCCCAGGAGG CTCCCATTCA AGTGAAGGAG GCAGACGAAA GGCCACAACA GTCGAGTGCA 600
CACTGTCAGA TGGCGATGAG GGCCAAGGAG GCACAGCAGC AGGGGAGGGG ATAGGGAAGG 660
CCCCGGTGGG CTGGGCTGCG TGAGCCACCT CTGACAAGGG TGCCTGGGAG CAGAGGCCCA 720
AAGGATTGGA CAGAACCAGC CATGTGGATC CTGGGGGAGA GGATCCAGGC TGAGGAAGCA 780
GCAAGGGCTC AGGCGAGAGC GGGAGTGCCC CCATCCTTTC CAAGAAACAC CCACGAGTCC 840
AGGGTCTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTATCTA TATGTGTGTG 900
TCTGTATGAG TATGTGTCTG TATGATGTCT GTGTGTCTTT ATGTGTGTGT GTCTGTGTAT 960
CTATATGTGT GTGTCTGTAT GTGTATGTGT CTGTATGATG TCTGTGTGTC TTTATGTGTG 1020
TGTCTGTGTG TATCTATGTG TGTATGTGTG TGTCTGTATG TGTATGTGTC TGTATGATGT 1080
CTGTGTGTCT TTATGTGTGT GTGTCTGTGT GTGTGTCTAT GTTCCTGGGT GTGTGTCTGT 1140
ATGTGTGTAC CTATATGTGT GTGTGTGTGT ATCTATATGT GTATGTGTCT GTATGTGCAT 1200
GTGTCTGTAT GATGTGTCTA TGTGTCTCTA TGTGTGTGTG TCTGTACGTG TGTGTGTATC 1260
TATATATGTG TCTGTGTGTC TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTTGGGA 1320
AATGGCAGTG GCAGGTGCAC TATATGGTGG AGACACTGGG TTTTAGGCTT TAATGAGTTT 1380
GGGTTTTACC CCCAAGAAAC TGGGGGTAAA AGAGGGAATA AAAGCAAAAC ATCCCATGCC 1440
CTCAAGGAAC GTCTAGTCCA GGATTAGAAG TGGGGCAGTC CCAGGAAGGA GCCATCTTGA 1500
CAGTGAATTC ACGCGGAAGA CGCGTGAACC CAGCTGGCCT GGAGAGACAG AGGTGCTTTG 1560
CAGGGCATGG GGAAGCCAGC AGGTCCCAGT CGAGAAACCT GGTTTTCTGT CTGGGTTGGT 1620
TGAAGACTCT TTGTCCCAGA AGGAGTCGCT TGTTTGCTTG TTCATCTTAA GTTTAAATTG 1680
AGAGAGGTTA ACGGCTTTTG CCTCAGAAGG CAGGCTGGCC TGGCAGGGTG TGTGTTGTGA 1740
GGTGCAGAAA CACATCTTCC CCAGCTGGCC TCACAGGCCA AGAAGCAGAT AATGTCTTCC 1800
TTCTGCCAGC TTCCCCGCAG CTTGGTTTTC CTGGGACAGT TCCTCCGCTG GAGGAAGGGA 1860
CAGGGGATGG GGACAGGGGA TGGAGGAGGA GTTGGGGAGA CCCTTCAGAG AGTGTGGCAG 1920
AAACACGTGT GTACAGGCTG GCACACGAGT CACAGAGGCA ACAGGGTGGC TGCGGGGAGA 1980
AATGTGAGCA GAGCTCATGC AATTGTCGTG AGTGAGTGCG CTCTCGCGGC TCTAAGGATT 2040
TGGGAAAACA ACTTGCAGAT CCAGGCATGT TTACGTAGGG AGGGGTGCCG TGTGCTGGAC 2100
CAGGTCCAGA ACTAAAAATA ACACAGTATT TCTGTGCCCA GCAAGAGCGC TAGCATCTGT 2160
GGGGTTTGCG TGGTGGGAAG AGTGTGGTTT CAGCTGAACC AGGCGCAGTG TGACCAGAAC 2220
AGTAGGAGGG AAGGCCAGGC CTGGGTGGGA GGCCCCAGGA TGGGCGGGGG AAGGACTGAG 2280
GGCGAAGGCC ATCCCAACTC GCAGCAGAAA AAGCCTCCAG GCGGTCACGG GCTGCCCATC 2340
TCGTGAGGCC AGATGTGGGT CCTCCTGCAT ATCTGAAACA GCACAGAGCA TTGGGGCAGC 2400
CTCCAAACCT CCCCTATAAG GAGCAGTTAA GGGATCCAGA GGGCGTGGCC TGGAGCAGAG 2460
AGAAGGGAAG CAACATGTGT GGGGCATTCA CAAGTGCAGG ATGCCTTCTC CGGGCTCCCA 2520
TGATGATCCA GACAGGTAGG CGTTTTCCTT CCCTTTTTGC AGATTGTGAA AACAGCGTTC 2580
AAAAAAGACT CATGGGCCGG GCGCGGTGGA TCACGCCTGT AATCCCAGCA CTTTGGGAGG 2640