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

TagContent
EnhancerAtlas ID
HS176-10649 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr12:120684510-120686730 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr12:120685635-120685656AAAGAAAAAAAGAAAGAAAGT-6.17
NFAT5MA0606.1chr12:120684890-120684900AATGGAAAAT-6.02
NFATC1MA0624.1chr12:120684890-120684900AATGGAAAAT-6.02
NFATC3MA0625.1chr12:120684890-120684900AATGGAAAAT-6.02
ZNF263MA0528.1chr12:120686353-120686374CCCTCTCTTCCCTCCTCCCCA-6.73
ZNF263MA0528.1chr12:120686350-120686371GTCCCCTCTCTTCCCTCCTCC-7.09
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_00357chr12:120684667-120690964Adipose_Nuclei
SE_00942chr12:120684944-120685582Adrenal_Gland
SE_00942chr12:120685787-120686779Adrenal_Gland
SE_02706chr12:120684829-120686788Astrocytes
SE_06253chr12:120685767-120689006Brain_Hippocampus_Middle
SE_09726chr12:120685440-120686826CD14
SE_18785chr12:120684752-120689039CD4p_CD25-_Il17-_PMAstim_Th
SE_20423chr12:120685587-120693557CD56
SE_25945chr12:120684604-120689033Duodenum_Smooth_Muscle
SE_27013chr12:120684994-120685643Esophagus
SE_27013chr12:120685802-120686829Esophagus
SE_27737chr12:120685632-120688866Fetal_Intestine
SE_28646chr12:120685504-120688776Fetal_Intestine_Large
SE_29635chr12:120684971-120689052Fetal_Muscle
SE_31816chr12:120685849-120686769Gastric
SE_34374chr12:120684958-120688837HCT-116
SE_35936chr12:120684494-120688727HMEC
SE_36961chr12:120682447-120689343HSMMtube
SE_37987chr12:120684481-120688828HUVEC
SE_40794chr12:120684754-120689058Left_Ventricle
SE_42203chr12:120684854-120688856Lung
SE_44237chr12:120684549-120686785NHDF-Ad
SE_44983chr12:120684822-120685568NHLF
SE_44983chr12:120685745-120686766NHLF
SE_46156chr12:120684613-120686834Osteoblasts
SE_47284chr12:120682425-120704730Panc1
SE_48117chr12:120684796-120685663Psoas_Muscle
SE_48117chr12:120685760-120686946Psoas_Muscle
SE_48648chr12:120685031-120685716Right_Atrium
SE_48648chr12:120685821-120686839Right_Atrium
SE_50261chr12:120685010-120686891Sigmoid_Colon
SE_51208chr12:120684541-120689036Skeletal_Muscle
SE_51764chr12:120684782-120686801Skeletal_Muscle_Myoblast
SE_52496chr12:120684912-120685605Small_Intestine
SE_52496chr12:120685695-120686887Small_Intestine
SE_53419chr12:120684890-120689016Spleen
SE_54833chr12:120684953-120686427Stomach_Smooth_Muscle
SE_55411chr12:120685912-120686605Thymus
SE_55760chr12:120682350-120688669u87
SE_63549chr12:120684765-120686741HSMM
SE_64693chr12:120684589-120686808NHEK
SE_65557chr12:120685592-120686571Pancreatic_islets
SE_67501chr12:120682350-120688669u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12120684919120685800
chr12120685110120686279
Enhancer Sequence
AGCTAGGCAT GGTGGTGCGT GCCTGTAGTC TCAGCTACTC AGGAGGCTGA GGCAGGAGAA 60
TCACTTGAAC CCGGGAGGCA GAGGTTGCAG TGAGCCAGGA TTGCGCCACT GCACTCCAGC 120
CTGGGCAATA GAGTGAGAAT CTGTCTTAAA AAAAAAAAAA AAAAGAAAAA TGTAGCCGGG 180
CATGTTAGCA TATGCCTGTA ATTCCAGCTA CTCGAGAGGC TAAGGCAGGA GGATCACTTG 240
AGCCTAGGAG TTTGACACTG TAGTAAGCCA TGACTGTACC ACTGCACTTC AGCCTGGGTG 300
ACAGCAAGAC CCTGTCTCTA TAAAAAAAAA TTTTAAAAAA AAGAAGGCTA GAAAAGAAGA 360
AAGAATAAAC AGATGGCACA AATGGAAAAT GAATGGCAAC ATGATAGACT TCAGTCTAAC 420
CACATTGATA ATTACTTTAA AATCTAAAAG GTTTATATAC TCCAATTAAA AGGCAGAGAT 480
TTTCAGCCTG GGTAGAAATG CAGTATTTAA TACATGCTAT CTACAAGAAA CATACTTTAC 540
ATATAAAGAC ACAGATAGAT TCAGTATAAA GCAATGGAGA AAGATATACC ATGCAAACAC 600
TAATATCAAG GAAGGCAGAG TGGCCCTTTG AGGGAGCCAG CTGGCAGCTG CCACTAAACT 660
CTGGTGTGCC CTCGCCTGCT CCTGAGTTGC CACTGTTTGC CCTCACCCCA GAACAAGTCA 720
GCTAGGAAGC CACACCACAG CTATGGCTTT CAAAGCCATC CGTGGAACTA GAGGTGGCAA 780
TTTATTAAAT CAGAATTACC CTAGCCTGCC GCAACATCAA ATCTCTGGAG AAGGTGTGTG 840
CTGACTTGAT CAGAGGTGCA AAGGAAAAGA ATCTCAAAGT GAAGGATCAG TTCAGATGCC 900
TATCAAGACT CTGAGAATCA CTATAAGAAA AACGCCTCGT GATGAAGGTT CTAGGACAAG 960
GGATCGTTTC CAGATGAGAA TCCGCAAGTG ACTCACTGAC CTGGATGGTC CTCCCGAGAT 1020
TGCTAAGCAG ATTACGTCCA TCTGTACTGA GCTGAGATTC AAGGTTAAAG TCACCACTGC 1080
AGATGTTTCA AGCAACTATT TTATTAACAG AATAGCAGTT GTTTAAAAGA AAAAAAGAAA 1140
GAAAGTTGAA GTGCTTCTGT TAATATCAGG CAAGGCAGAC TTCCAGACAG GAATATTACC 1200
AGAGGTAAAG AGGGACATTT CATAATGATG AGTCAATTCA TCATGAAGAC ATAATCATCC 1260
TAAATGTACA CCCACTCAAC AACAGAGCTC TAAAGTAGAT AAAGCAAAAA TGGACAAAAT 1320
TGAAAAGAAA AAGTGACAAA TCCACAATCC TAGTTGGAAA CTGGAGACTT TGACTCTCCA 1380
GTTGAGAAAG CTCAATAATT GAGAAAAAAC TCTTCCAAAG GAAGCCAGTG GAAGATATAA 1440
GCAAATAACC CAAGAGAGGT GAAGAGCAGG AGGACAGAGG GCTGCCAGAC TGCTGGTCTG 1500
GGGAACATGA GGGACCCCAG CCTTTGCTCA CGGTAGAAGA GGGGGCTGGA GGATGGCCAC 1560
AGAGCAGGAA ATGCTCCCTC CTCTGTCCAC AGCCCCTAGA CCTTCCCCAG AGGGAAGCAC 1620
GCCAGCTCAC ACCACACTTC TCCTGGGGTC ATTTTCAGTC CCTGATAACC CTGGATAGGG 1680
GTCAGTGTTC AACAGCCCCC ACTGCCCTCA GCAGACACCT GGTTGACTAT GTTTCCTCAA 1740
TTACTGCACC CCCAAGCACA CCATATACAA TCCACAGATG ACTTTCACAC ACACACACAC 1800
ACACACACAC ACACACACAC ACACACACAC ACACCAGACT GTCCCCTCTC TTCCCTCCTC 1860
CCCAGTGGCA CCGCGTGGCA TCACCCTCAT TGGCGAGCAG GAATCAGAAC AGAGTCTACA 1920
ATGTCAGCAA AGGGCTGTAT GCGACAGTCA CTGAATCCAA TCCCAGCTCC ACCACTAATC 1980
AGCAACTAAC CTCGGGCAAG TTGCTCACCT CTCTGTGCTT CAGTGTCGTC AGCTAGAATA 2040
CCTACTTCAG AGGGCTGTTG TGAGGAAATG ATAAGGGAAC GTAAGGGAGG TATTTAGAAC 2100
AGTGGCTGCC ACAGAGTGAG TAACACTATA TTAATGCTGG CAGTTATGGC CAGGTGCAGT 2160
GGTTCACGTC TGTAATCCCA AAACTTTGGG AGGCTGAGGC GGGTGGATCA CCTGAGGTCA 2220