EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS118-09132 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr19:11204920-11207580 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr19:11205882-11205896AAGAAATGAGTCAT+7.12
JUN(var.2)MA0489.1chr19:11207063-11207077ATGACTCATTTCTT-7.12
JUN(var.2)MA0489.1chr19:11207058-11207072AGGAAATGACTCAT+8.12
JUN(var.2)MA0489.1chr19:11205887-11205901ATGAGTCATTTCCT-8.12
SREBF1MA0595.1chr19:11205756-11205766GTGGGGTGAT-6.02
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_01022chr19:11203682-11206319Adrenal_Gland
SE_01022chr19:11206333-11207663Adrenal_Gland
SE_12085chr19:11204949-11207773CD3
SE_14622chr19:11198676-11207877CD4_Memory_Primary_7pool
SE_17142chr19:11204971-11207608CD4p_CD225int_CD127p_Tmem
SE_19715chr19:11204867-11207840CD4p_CD25-_Il17p_PMAstim_Th17
SE_20994chr19:11198676-11207604CD8_Memory_7pool
SE_22774chr19:11204855-11208057CD8_primiary
SE_23239chr19:11203891-11206070Colon_Crypt_1
SE_23239chr19:11206100-11207601Colon_Crypt_1
SE_24095chr19:11204989-11205979Colon_Crypt_2
SE_24095chr19:11206366-11207012Colon_Crypt_2
SE_24095chr19:11207130-11207564Colon_Crypt_2
SE_24928chr19:11205061-11206082Colon_Crypt_3
SE_24928chr19:11206201-11206876Colon_Crypt_3
SE_26902chr19:11204916-11207828Esophagus
SE_28429chr19:11198835-11207741Fetal_Intestine
SE_29308chr19:11199027-11207595Fetal_Intestine_Large
SE_29905chr19:11204956-11208148Fetal_Muscle
SE_31737chr19:11204927-11207763Gastric
SE_34726chr19:11198191-11208606HeLa
SE_36050chr19:11204941-11207563HMEC
SE_38264chr19:11198668-11208150HUVEC
SE_40068chr19:11198411-11207591K562
SE_42817chr19:11199051-11207805Lung
SE_44493chr19:11205013-11206118NHDF-Ad
SE_44493chr19:11206328-11207705NHDF-Ad
SE_44932chr19:11205113-11207883NHLF
SE_47693chr19:11204994-11205972Pancreas
SE_47693chr19:11206368-11206786Pancreas
SE_47693chr19:11207237-11207566Pancreas
SE_49361chr19:11205119-11206191Right_Atrium
SE_49361chr19:11206197-11207709Right_Atrium
SE_50772chr19:11198863-11207767Sigmoid_Colon
SE_52540chr19:11198883-11208401Small_Intestine
SE_54059chr19:11198844-11207806Spleen
SE_57847chr19:11205007-11205595VACO_503
SE_64571chr19:11204940-11207695NHEK
SE_65732chr19:11198652-11207882Pancreatic_islets
SE_68998chr19:11207123-11207544H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr191120695311207150
chr191120569611206011
Enhancer Sequence
AGCGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCATGCA CCACCACGCC 60
CGGCTAATTT TGTATTTTTC GTAGAGATGG GGTTTCTCCA CATTGGTTCA GGCTGTTCTC 120
GAACTCCCAA CCTCAGGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG GATTATAGGC 180
GTGAGCCCCC GAACCCGGCC ACTCCCAGCT AAGTTTAAAT TTTTTGTTTG TTTGTTCGTT 240
TGTTTTTATT TTTTGAGACA GAGTCTCCCG CCCAGGCTGG AGCGCAGATC ACTGCATCCT 300
TGACCTCCCA GGCTTAAGCC ATCCTCCCCA CTCAGCCTCC CAAGTAGCTG GGATTACAGG 360
TGTGTGCCAC TATGCTTGGC TAAGTTGTGT ATTTTTTGTA GAGATGGGGT TCAAGGGATT 420
CTCGCTTTGT TGCCTCGGTT GGTCTCAAAC TCCTGGGCTC AAGCAGTCCT CCCTCCTCAG 480
CCTCCCAAGG TGCTGGGGAA ATCCACTTTT GAAACATTGT CTGGAGAGTT GCCCAGGTGG 540
TAGATCACAG AAATAGGTCA TCGTGGGGTC CTTCCCATGG GTGCAGTCTT GAGCCACCTG 600
TGGCCAGCAA ATATTTGGAG AATAATAGTC AGGGGAGAGC TTGAGGTCCA GGGAAAGGTT 660
TTGTTTTTCT TCAGGGAAAG GTTTTTATTG TTCTTTATCC CTCCTTAAAG GACCTTCAGG 720
TGTTACTGAC ATTCCCGGTC TACCCAGTGG CACATTTAGT TTGTAAGCTG GGCCCTCGTA 780
CAGAGGTAGG GAGGTGAGAG CATTGGATTA GTGGTCACCA AAGCTGCGGT CACCTAGTGG 840
GGTGATCAGA GGCTCCTCCC TTAAGATCTT GATTGCCAAC GCCTCTGGCC CAACTTTCCT 900
TTTTATTTAT CGCAAGCCTC CTGGAATCTC AATTGCTTTT TGCCCACCCG GTGTGTCAGC 960
ACAAGAAATG AGTCATTTCC TCCTTTAAGC ACAGTTGAAA TTGAGCTGTG AGTCAGTGAG 1020
GTGTGTACGA TATTGTCAAA GCGGGGTGTG TACAGTATTG ACAGATCTGT AGTTGGGCAA 1080
GAGAATTATC AGAGTTTGTG ACCACAGCAG ATTCCAAAGC TCGACTCATT TTCTTCTCTC 1140
TTCCTTCCCT TTTTTCTTTT CTTTTTTTTT TTTTTTTTGA CAGAGTCTCG CTCTGTTGCC 1200
CAGGCTGGAG TGCAGTGGCA CAATCTGGGC TCACTGCAGC CCCTGCCTCC TGGGTTCAAA 1260
TGATTCTCAT GTTTCAGCCT CCCGAGTAGC TGCAATTACA GGCATTCGGG TTCAAGTGAT 1320
TCTCCTGCCT CAGCCACCTG AGCAGCTGGG ATTACAGGCG CCCGCCACCA CGCCCGGCTA 1380
ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CACCATGTTG GCCAGGCTGG TCTCGAACTC 1440
CTGAACTCAG GTGATCCGCC CACTTCGGCC TCCCAAAGTG CTGAGATTAC AGACGTGAGT 1500
CACCGCGCCC AGCCTGTTCT GTTCTTTAAT TCTCAAAACA CCCTCTAGGA AGTAGAGACT 1560
GCCATTCTCC CCCATTTTAC AGATCAGGAA ACTGAGTCCC AGAAGGATTT AGTCAGTTAC 1620
CCAAGTTGTT CTAGTTAAAT GGCCTGGAAA GCCAGTGAAG CCCAGGATTG TCTATCTAAC 1680
CCCCTTACTA CTCTAACTTT CAGGGAATCC ACATGAATGT GCTGGGTCAA CCATCAAAGT 1740
TGAAATGGAT AAAGGGGGCT GGATGCGGTG GCTGATGCCT GTAATCCTAG CACTTTGGGA 1800
GGCCGAGATG GGTGGGTGGA TTGCTTGAGC CCAAGAGTTT GAGACCAGCC TGGGCAACAT 1860
AGTGAGACAC CTGTCTCTGC AAAAAATAAA TAAAAAGTTA GCTGAGTGTG ATGGTGCACC 1920
CCTCTAGTCA CAGCTGTTGA GTTAGGCTTA GGCAGGAGGA TCGCATGAAC CTGGGAGGTG 1980
GAGGCGGCCG TGAGCCTCAG TCATGCCACT GCACTCCAAC CTGGGCAACA GAGTGAAAGC 2040
CGGTGTCCGA AAGAGAAAGA AAAAAAGACA TAGATACATC TTTTAAAGTT AGGTTGTATG 2100
TTAATTACCT ACAACTCAGT TTCAACTGTG CTTAAAGGAG GAAATGACTC ATTTCTTGCT 2160
ACATATCAAA TTAGCCCAAA ATGTAGTGGC TTAAAACAAC ACATTTATGA TTTCTCAGTT 2220
TTTGCGTGTC AGGAATTTGG AAGCAGCACA GCTAGACGGT TCCAGCTCAG GGTCTCTCAT 2280
GAAGTTGCAA TCAAAATATT GGCAGGAGAG AAAAACATAT TTTCAGAAGC TGCAGGCATA 2340
GGAAGACTTG GCTGGGGTTG AAGGATCCAC TTCCAAGATG GCGCACTCAG TGGCTCTTGG 2400
CTGGAGGCCT CAGTTCCCTG CTGCGTGGAG CTCTCCCTCC AGCTGCTTGA GTGGACTCAT 2460
GACATGCAGC TGGCCTCCCC TGGAGCAGTC GATCCAACAA TGAGCATGGC CATGAACTAG 2520
GCTCAGAAGC CACTCCCTGT CGTCTCTACA TTTTCCTATC AGAAGCAAGT CATTAAAAGT 2580
CCAGTGCCAC TCCAGGGGAG ACGAATTAGG CTCTGCCTTC TGAAAGGATT ATCACAGAAG 2640
ATGCGGTCCT ATATTCTTTT 2660